Mental retardation, anterior maxillary protrusion, and strabismus

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Results for "Mental retardation, anterior maxillary protrusion, and strabismus": 1003 gene sets

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Mental retardation, anterior maxillary protrusion, and strabismus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.
mental retardation, anterior maxillary protrusion, and strabismus Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated OMIM Gene-Disease Associations dataset.
Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
scaphocephaly, maxillary retrusion, and mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the scaphocephaly, maxillary retrusion, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cystic fibrosis; maxillary sinusitis; sinusitis, maxillary Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; maxillary sinusitis; sinusitis, maxillary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation with language impairment and autistic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with mental retardation and digital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia, cerebellar ataxia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alacrima, achalasia, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skeletal defects, genital hypoplasia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth deficiency and mental retardation with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset.
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset.
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.
Cleft Palate, Isolated, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cleft Palate, Isolated, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Microcephaly with Mental Retardation and Digital Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly with Mental Retardation and Digital Anomalies from the curated CTD Gene-Disease Associations dataset.
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Cubitus Valgus with Mental Retardation and Unusual Facies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cubitus Valgus with Mental Retardation and Unusual Facies from the curated CTD Gene-Disease Associations dataset.
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset.
epilepsy and mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy and mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation, severe, with spasticity and tapetoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, severe, with spasticity and tapetoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation with language impairment and autistic features Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation with language impairment and autistic features phenotype from the curated OMIM Gene-Disease Associations dataset.
?rolandic epilepsy, mental retardation, and speech dyspraxia Gene Set From OMIM Gene-Disease Associations genes associated with the ?rolandic epilepsy, mental retardation, and speech dyspraxia phenotype from the curated OMIM Gene-Disease Associations dataset.
skeletal defects, genital hypoplasia, and mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia Gene Set From OMIM Gene-Disease Associations genes associated with the corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.
alacrima, achalasia, and mental retardation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the alacrima, achalasia, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
?arthrogryposis, mental retardation, and seizures Gene Set From OMIM Gene-Disease Associations genes associated with the ?arthrogryposis, mental retardation, and seizures phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.
?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
choroideremia, deafness, and mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the choroideremia, deafness, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
cubitus valgus with mental retardation and unusual facies Gene Set From OMIM Gene-Disease Associations genes associated with the cubitus valgus with mental retardation and unusual facies phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, focal, with speech disorder and with or without mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 29 and others Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 29 and others phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, spastic quadriplegia, and mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) phenotype from the curated OMIM Gene-Disease Associations dataset.
coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis Gene Set From OMIM Gene-Disease Associations genes associated with the alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis phenotype from the curated OMIM Gene-Disease Associations dataset.
Alport Syndrome, Mental Retardation, Midface Hypoplasia, And Elliptocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, And Elliptocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Iris Coloboma With Ptosis, Hypertelorism, And Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Iris Coloboma With Ptosis, Hypertelorism, And Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, And Obesity Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, And Obesity Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alacrima, Achalasia, And Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alacrima, Achalasia, And Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hydronephrosis, Congenital, With Cleft Palate, Characteristic Facies, Hypotonia, And Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hydronephrosis, Congenital, With Cleft Palate, Characteristic Facies, Hypotonia, And Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Deficiency And Mental Retardation With Facial Dysmorphism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Deficiency And Mental Retardation With Facial Dysmorphism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryohydrocytosis, Stomatin-Deficient, With Mental Retardation, Seizures, Cataracts, And Massive Hepatosplenomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryohydrocytosis, Stomatin-Deficient, With Mental Retardation, Seizures, Cataracts, And Massive Hepatosplenomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coloboma, Cleft Lip-Palate And Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coloboma, Cleft Lip-Palate And Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) pathway from the Reactome Pathways 2024 dataset.
Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) pathway from the Reactome Pathways 2024 dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia, mental retardation and dysequlibrium syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia, mental retardation and dysequlibrium syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
protrusion Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term protrusion in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
RNA polymerase, beta subunit, protrusion Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RNA polymerase, beta subunit, protrusion protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lateral Protrusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lateral Protrusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Protrusion Of Tongue Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Protrusion Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Incisor Protrusion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Incisor Protrusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
rDNA protrusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the rDNA protrusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Ear protrusion Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ear protrusion phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Metaphyseal Dysplasia With Maxillary Hypoplasia And Brachydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metaphyseal Dysplasia With Maxillary Hypoplasia And Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-linked mental retardation 58 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation 58 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked 45 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation, syndromic, Claes-Jensen type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation, syndromic, Claes-Jensen type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation 63 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation 63 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked, syndromic, turner type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked, syndromic, turner type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 30 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-Linked mental retardation 90 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-Linked mental retardation 90 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked syndromic 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked syndromic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 27 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 29 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Syndromic X-linked mental retardation 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Syndromic X-linked mental retardation 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Siderius X-linked mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with marfanoid habitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wilson-Turner X-linked mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wilson-Turner X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked, syndromic, raymond type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked, syndromic, raymond type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation, syndromic 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation, syndromic 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Birk Barel mental retardation dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Birk Barel mental retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ZNF711-Related X-linked Mental Retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ZNF711-Related X-linked Mental Retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 27 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation, with or without seizures, ARX-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 39 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal epilepsy with speech disorder with or without mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 38 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 38 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 34 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 34 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked, syndromic 32 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked, syndromic 32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked, syndromic, wu type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked, syndromic, wu type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-Linked Mental Retardation 41 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-Linked Mental Retardation 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked, syndromic, Hedera type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked, syndromic, Hedera type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked syndromic mental retardation, Nascimento type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked syndromic mental retardation, Nascimento type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 47 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 47 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked, nonspecific Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation 30 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked, syndromic 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked, syndromic 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 40 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 40 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 41 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 42 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 42 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 43 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 43 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 44 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 44 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 45 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 46 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 46 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked 93 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked 93 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked 96 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked 96 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked 98 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked 98 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked 99 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked 99 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, X-linked 72 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, X-linked 72 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Siderius X-linked mental retardation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Siderius X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.
Partington X-linked mental retardation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Partington X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.
Alopecia-Mental Retardation Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia-Mental Retardation Syndrome 1 from the curated CTD Gene-Disease Associations dataset.
Alopecia-Mental Retardation Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia-Mental Retardation Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 30 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 30 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 13 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 23 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 23 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 91 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 91 from the curated CTD Gene-Disease Associations dataset.
Miles-Carpenter x-linked mental retardation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miles-Carpenter x-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 95 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 95 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 9 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 77 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 77 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, Syndromic 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 13 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, Syndromic 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 12 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, Syndromic 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 14 from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.
Lubs X-linked mental retardation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lubs X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Fra12a Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Fra12a Type from the curated CTD Gene-Disease Associations dataset.
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, with Short Stature Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, with Short Stature from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 20 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 20 from the curated CTD Gene-Disease Associations dataset.
Mental retardation X-linked syndromic 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation X-linked syndromic 7 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Dominant 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Dominant 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 5 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Dominant 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 4 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 17 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 17 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, Syndromic, Jarid1c-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Jarid1c-Related from the curated CTD Gene-Disease Associations dataset.
X-linked mental retardation Gustavson type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease X-linked mental retardation Gustavson type from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Female-Restricted, with Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Female-Restricted, with Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 81 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 81 from the curated CTD Gene-Disease Associations dataset.
Mental retardation, X-linked 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked 14 from the curated CTD Gene-Disease Associations dataset.
Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type from the curated CTD Gene-Disease Associations dataset.
Mental retardation-hypotonic facies syndrome, x-linked, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation-hypotonic facies syndrome, x-linked, 1 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, Syndromic, Christianson Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Christianson Type from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 84 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 84 from the curated CTD Gene-Disease Associations dataset.
Mental retardation, X-linked, syndromic 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, syndromic 5 from the curated CTD Gene-Disease Associations dataset.
BRACHYDACTYLY-MENTAL RETARDATION SYNDROME Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BRACHYDACTYLY-MENTAL RETARDATION SYNDROME from the curated CTD Gene-Disease Associations dataset.
Birk-Barel Mental Retardation Dysmorphism Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Birk-Barel Mental Retardation Dysmorphism Syndrome from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.
MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, X-LINKED 21 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 21 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, with Epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, with Epilepsy from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 9 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 78 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 78 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 73 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 73 from the curated CTD Gene-Disease Associations dataset.
Abidi X-linked mental retardation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Abidi X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 4 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 82 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 82 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 11 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 10 from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, X-LINKED 96 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 96 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 8 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 7 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 6 from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, X-LINKED 49 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 49 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, With Panhypopituitarism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, With Panhypopituitarism from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 52 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 52 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 53 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 53 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 58 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 58 from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Recessive 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 1 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 63 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 63 from the curated CTD Gene-Disease Associations dataset.
Armfield X-Linked Mental Retardation Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Armfield X-Linked Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 42 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 42 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 93 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 93 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 94 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 94 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, Syndromic, Turner Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Turner Type from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 72 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 72 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 45 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 45 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 46 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 46 from the curated CTD Gene-Disease Associations dataset.
Prieto X-linked mental retardation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prieto X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, Syndromic 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 10 from the curated CTD Gene-Disease Associations dataset.
Martin-Probst Deafness-Mental Retardation Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Martin-Probst Deafness-Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked 50 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked 50 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Dominant 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.
Parkinsonism, early onset with mental retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinsonism, early onset with mental retardation from the curated CTD Gene-Disease Associations dataset.
non-specific x-linked mental retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease non-specific x-linked mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
epilepsy; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation; rett syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
language development disorders; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease language development disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x syndrome; mental retardation; spinocerebellar degenerations; tremor Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x syndrome; mental retardation; spinocerebellar degenerations; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x syndrome; fragile x syndromes; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x syndrome; fragile x syndromes; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation; muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
violent offenders with mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease violent offenders with mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukomalacia, periventricular; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease leukomalacia, periventricular; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
non-syndromic x-linked mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease non-syndromic x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain diseases; mental retardation, x-linked Gene Set From GAD Gene-Disease Associations genes associated with the disease brain diseases; mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital abnormalities; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital abnormalities; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
learning disorders; memory disorders; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease learning disorders; memory disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
x-linked mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation, x-linked Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation, x-linked; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation, x-linked; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation; microcephaly Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation; microcephaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Mental Retardation, X-Linked Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Retardation, X-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Retardation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Retardation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Nuclear fragile X mental retardation-interacting protein 1, conserved domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear fragile X mental retardation-interacting protein 1, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Fragile X mental retardation protein family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Fragile X mental retardation protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
mental retardation, autosomal recessive, 9/26 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive, 9/26 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 19 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 18 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 10 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 13 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 12 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 15 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 14 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 17 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 16 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 84 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 84 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 81 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 81 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 82 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 82 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 89 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 89 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 28 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 28 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 29 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 29 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 23 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 27 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 24 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 25 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 30 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 30 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 9 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 8 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 1 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 3 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 2 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 5 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 4 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 7 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 6 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, snyder-robinson type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, snyder-robinson type phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 30/47 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 30/47 phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, x-linked syndromic 10 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, x-linked syndromic 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation syndrome, x-linked, siderius type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation syndrome, x-linked, siderius type phenotype from the curated OMIM Gene-Disease Associations dataset.
alpha-thalassemia/mental retardation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the alpha-thalassemia/mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic 16 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 40 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 40 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 44 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 44 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 46 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 46 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, fraxe type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, fraxe type phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation syndrome, x-linked, armfield type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation syndrome, x-linked, armfield type phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, x-linked, syndromic 12 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, x-linked, syndromic 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperphosphatasia with mental retardation syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperphosphatasia with mental retardation syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperphosphatasia with mental retardation syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperphosphatasia with mental retardation syndrome 4 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, with isolated growth hormone deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, with isolated growth hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, x-linked, syndromic, hedera type Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, x-linked, syndromic, hedera type phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, x-linked 91 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, x-linked 91 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 90 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 90 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 98 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 98 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 32 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 32 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic, shashi type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic, shashi type phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation-hypotonic facies syndrome, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation-hypotonic facies syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, autosomal dominant 22 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, autosomal dominant 22 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 30 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 30 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 78 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 78 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 72 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 72 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 3 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 2 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 7 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, syndromic 32 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, syndromic 32 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 52 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 52 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 53 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 53 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 50 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 50 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 58 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 58 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, syndromic, claes-jensen type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, syndromic, claes-jensen type phenotype from the curated OMIM Gene-Disease Associations dataset.
waisman parkinsonism-mental retardation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the waisman parkinsonism-mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic, nascimento-type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic, nascimento-type phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 21/34 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 21/34 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 31 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 31 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, syndromic 13 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, syndromic 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, syndromic 17 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, syndromic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, syndromic 14 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, syndromic 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 10/20 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 10/20 phenotype from the curated OMIM Gene-Disease Associations dataset.
?stocco dos santos x-linked mental retardation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?stocco dos santos x-linked mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 19 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 14 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
birk-barel mental retardation dysmorphism syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the birk-barel mental retardation dysmorphism syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 77 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 77 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 9 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 1 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 2 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, syndromic 15 (cabezas type) Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, syndromic 15 (cabezas type) phenotype from the curated OMIM Gene-Disease Associations dataset.
brachydactyly-mental retardation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the brachydactyly-mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, with short stature Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, with short stature phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, autosomal recessive 45 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, autosomal recessive 45 phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, autosomal recessive 42 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, autosomal recessive 42 phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, autosomal recessive 43 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, autosomal recessive 43 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, syndromic, chudley-schwartz type, Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, syndromic, chudley-schwartz type, phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 92 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 92 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 93 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 93 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 96 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 96 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 97 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 97 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 94 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 94 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 95 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 95 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 99 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 99 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 39 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 39 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 38 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 38 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 31 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 31 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 33 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 33 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 35 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 35 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 34 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 34 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 36 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 36 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia-mental retardation syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia-mental retardation syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia-mental retardation syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia-mental retardation syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia-mental retardation syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia-mental retardation syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 21 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 23 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 24 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 26 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 26 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 29 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 29 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation-skeletal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation-skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 13 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 12 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 16 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 15 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 14 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 19 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 18 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic, raymond type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic, raymond type phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, nonprogressive, with mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, nonprogressive, with mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic, abidi type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic, abidi type phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, with or without nystagmus Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic 7 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic 5 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
alpha-thalassemia/mental retardation syndrome, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the alpha-thalassemia/mental retardation syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
?hyperphosphatasia with mental retardation syndrome 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ?hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 41 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 41 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 63 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 63 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 5 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, x-linked 101 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, x-linked 101 phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, x-linked 100 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, x-linked 100 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic, turner type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic, turner type phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 49 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 49 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 41 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 41 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 42 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 42 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 45 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 45 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 46 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 46 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic, lubs type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic, lubs type phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, autosomal dominant 11 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, autosomal dominant 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 23 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked 20 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal recessive 1 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant, 27 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, fra12a type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, fra12a type phenotype from the curated OMIM Gene-Disease Associations dataset.
megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, autosomal recessive, 37 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, autosomal recessive, 37 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant, 28 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant, 28 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked syndromic, christianson type Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked syndromic, christianson type phenotype from the curated OMIM Gene-Disease Associations dataset.
Mild Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mandibulofacial Dysostosis With Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mandibulofacial Dysostosis With Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Profound Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Profound Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alpha-Thalassemia/Mental Retardation Syndrome, Nondeletion Type, X-Linked Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alpha-Thalassemia/Mental Retardation Syndrome, Nondeletion Type, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partington X-Linked Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partington X-Linked Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Miles-Carpenter X-Linked Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miles-Carpenter X-Linked Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prieto X-Linked Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prieto X-Linked Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lubs X-Linked Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lubs X-Linked Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Siderius X-Linked Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Siderius X-Linked Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alpha-Thalassemia/Mental Retardation Syndrome (301040) Is An Allelic Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alpha-Thalassemia/Mental Retardation Syndrome (301040) Is An Allelic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Birk-Barel Mental Retardation Dysmorphism Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Birk-Barel Mental Retardation Dysmorphism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Martin-Probst Deafness-Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Martin-Probst Deafness-Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH) pathway from the Reactome Pathways 2024 dataset.
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
alopecia-mental retardation syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alopecia-mental retardation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nonprogressive cerebellar ataxia with mental retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nonprogressive cerebellar ataxia with mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
alopecia-mental retardation syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alopecia-mental retardation syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked mental retardation-hypotonic facies syndrome-1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked mental retardation-hypotonic facies syndrome-1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Strabismus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Strabismus from the curated CTD Gene-Disease Associations dataset.
strabismus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease strabismus from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
strabismus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease strabismus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
strabismus Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term strabismus in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
strabismus Gene Set From HPO Gene-Disease Associations genes associated with the strabismus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital strabismus Gene Set From HPO Gene-Disease Associations genes associated with the congenital strabismus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Strabismus Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Strabismus protein domain from the InterPro Predicted Protein Domain Annotations dataset.
{strabismus, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {strabismus, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
Strabismus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Strabismus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Strabismus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Strabismus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paralytic Strabismus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paralytic Strabismus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Incomitant Strabismus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Incomitant Strabismus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Strabismus Fixus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Strabismus Fixus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Monocular Strabismus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Monocular Strabismus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Strabismus, Comitant Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Strabismus, Comitant in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Strabismus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Strabismus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Strabismus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Strabismus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mechanical strabismus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mechanical strabismus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Strabismus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Strabismus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-strabismus syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-strabismus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; hellp syndrome; intrauterine growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; intrauterine growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Anterior hypothalamic nucleus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
abnormal anterior commissure pars anterior morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal anterior commissure pars anterior morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal anterior commissure pars anterior morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal anterior commissure pars anterior morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Maxillary Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Maxillary Diseases from the curated CTD Gene-Disease Associations dataset.
Maxillary Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Maxillary Neoplasms from the curated CTD Gene-Disease Associations dataset.
maxillary sinus cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease maxillary sinus cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acute maxillary sinusitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute maxillary sinusitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
maxillary sinus squamous cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease maxillary sinus squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
maxillary sinusitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease maxillary sinusitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
maxillary sinus adenoid cystic carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease maxillary sinus adenoid cystic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic maxillary sinusitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic maxillary sinusitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; maxillary neoplasms; mouth neoplasms; tongue neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; maxillary neoplasms; mouth neoplasms; tongue neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
maxillary Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term maxillary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
agenesis of maxillary lateral incisor Gene Set From HPO Gene-Disease Associations genes associated with the agenesis of maxillary lateral incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
agenesis of maxillary incisor Gene Set From HPO Gene-Disease Associations genes associated with the agenesis of maxillary incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peg-shaped maxillary lateral incisors Gene Set From HPO Gene-Disease Associations genes associated with the peg-shaped maxillary lateral incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
widely-spaced maxillary central incisors Gene Set From HPO Gene-Disease Associations genes associated with the widely-spaced maxillary central incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
supernumerary maxillary incisor Gene Set From HPO Gene-Disease Associations genes associated with the supernumerary maxillary incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macrodontia of permanent maxillary central incisor Gene Set From HPO Gene-Disease Associations genes associated with the macrodontia of permanent maxillary central incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
single median maxillary incisor Gene Set From HPO Gene-Disease Associations genes associated with the single median maxillary incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Maxillary Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Maxillary Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Maxillary Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Maxillary Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Maxillary Sinusitis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Maxillary Sinusitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal maxillary sinus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent maxillary shelf Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent maxillary shelf phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal maxillary nerve morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal maxillary prominence morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
maxillary shelf hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the maxillary shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased maxillary shelf size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased maxillary shelf size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal maxillary shelf morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary shelf morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
single median maxillary central incisor Gene Set From OMIM Gene-Disease Associations genes associated with the single median maxillary central incisor phenotype from the curated OMIM Gene-Disease Associations dataset.
metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
maxillary nerve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue maxillary nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Maxillary Sinus Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Maxillary Sinus Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Solitary Median Maxillary Central Incisor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Solitary Median Maxillary Central Incisor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Maxillary Sinusitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Maxillary Sinusitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Maxillary Sinus Squamous Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Maxillary Sinus Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supernumerary Maxillary Incisor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supernumerary Maxillary Incisor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Maxillary Sinusitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Maxillary Sinusitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Maxillary Sinusitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Maxillary Sinusitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Maxillary Retrusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Maxillary Retrusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metaphyseal Dysplasia With Maxillary Hypoplasia With Or Without Brachydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metaphyseal Dysplasia With Maxillary Hypoplasia With Or Without Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Widely-Spaced Maxillary Central Incisors Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widely-Spaced Maxillary Central Incisors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peg-Shaped Maxillary Lateral Incisors Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peg-Shaped Maxillary Lateral Incisors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Maxillary Retroposition Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maxillary Retroposition in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
absent maxillary shelf Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent maxillary shelf phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal maxillary zygomatic process morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary zygomatic process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged maxillary zygomatic process Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged maxillary zygomatic process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal maxillary shelf morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary shelf morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased maxillary shelf size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased maxillary shelf size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal maxillary prominence morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary prominence morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent maxillary sinus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent maxillary sinus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
maxillary shelf hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the maxillary shelf hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal maxillary nerve morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary nerve morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal maxillary-premaxillary suture morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary-premaxillary suture morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
maxillary retrognathia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the maxillary retrognathia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal maxillary dental arch morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary dental arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal maxillary frontal process morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary frontal process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
maxillary sinus inflammation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the maxillary sinus inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
maxillary cyst Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the maxillary cyst phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature maxillary-premaxillary suture closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature maxillary-premaxillary suture closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small maxillary prominence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small maxillary prominence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent maxillary prominence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent maxillary prominence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
maxillary zygomatic process hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the maxillary zygomatic process hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Maxillary sinusitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinusitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic maxillary sinusitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic maxillary sinusitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acute maxillary sinusitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute maxillary sinusitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary sinus squamous cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinus squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary sinus cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinus cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Solitary median maxillary central incisor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Solitary median maxillary central incisor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary sinus adenoid cystic carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinus adenoid cystic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary sinus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary sinus adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinus adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary sinus inverted papilloma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinus inverted papilloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary nerve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Maxillary nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Solitary median maxillary central incisor syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Solitary median maxillary central incisor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Tooth agenesis (maxillary lateral incisors) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Tooth agenesis (maxillary lateral incisors) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Tooth agenesis (maxillary second premolars) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Tooth agenesis (maxillary second premolars) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Abstraction and mental flexibility Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abstraction and mental flexibility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.
psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From OMIM Gene-Disease Associations genes associated with the psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated OMIM Gene-Disease Associations dataset.
severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set From OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated OMIM Gene-Disease Associations dataset.
growth retardation, developmental delay, coarse facies, and early death Gene Set From OMIM Gene-Disease Associations genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.
Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychomotor Retardation, Epilepsy, And Craniofacial Dysmorphism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychomotor Retardation, Epilepsy, And Craniofacial Dysmorphism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Pre- And Postnatal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Growth Retardation, Pre- And Postnatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypotonia with psychomotor retardation and characteristic facies-3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypotonia with psychomotor retardation and characteristic facies-3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and anterior segment dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sacral defect and anterior sacral meningocele Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.
Foveal Hypoplasia and Anterior Segment Dysgenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset.
thorax and anterior abdomen determination Gene Set From GO Biological Process Annotations 2015 genes participating in the thorax and anterior abdomen determination biological process from the curated GO Biological Process Annotations 2015 dataset.
craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set From OMIM Gene-Disease Associations genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
Anterior Segment Anomalies And Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Segment Anomalies And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sacral Defect And Anterior Sacral Meningocele Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sacral Defect And Anterior Sacral Meningocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Foveal Hypoplasia And Anterior Segment Dysgenesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Foveal Hypoplasia And Anterior Segment Dysgenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Craniofacial Anomalies And Anterior Segment Dysgenesis Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Craniofacial Anomalies And Anterior Segment Dysgenesis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
thorax and anterior abdomen determination Gene Set From GO Biological Process Annotations 2023 genes participating in the thorax and anterior abdomen determination biological process from the curated GO Biological Process Annotations 2023 dataset.
thorax and anterior abdomen determination Gene Set From GO Biological Process Annotations 2025 genes participating in the thorax and anterior abdomen determination biological process from the curated GO Biological Process Annotations 2025 dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aniridia cerebellar ataxia mental deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aniridia cerebellar ataxia mental deficiency from the curated CTD Gene-Disease Associations dataset.
Mental Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Disorders from the curated CTD Gene-Disease Associations dataset.
MENTAL HEALTH WELLNESS 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL HEALTH WELLNESS 1 from the curated CTD Gene-Disease Associations dataset.
Growth mental deficiency syndrome of Myhre Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth mental deficiency syndrome of Myhre from the curated CTD Gene-Disease Associations dataset.
Mental Disorders Diagnosed in Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Disorders Diagnosed in Childhood from the curated CTD Gene-Disease Associations dataset.
MENTAL HEALTH WELLNESS 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL HEALTH WELLNESS 2 from the curated CTD Gene-Disease Associations dataset.
Mental Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Mental Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Mental Competency Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Mental Competency in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Mental Processes Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Mental Processes in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
developmental disorder of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease developmental disorder of mental health from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
disease of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease disease of mental health from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
mental depression Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease mental depression in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
disease of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease disease of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
mental depression Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mental depression in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcohol-induced mental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
disease of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease disease of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental disorder of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
drug-induced mental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease drug-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mental development Gene Set From GAD Gene-Disease Associations genes associated with the disease mental development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease mental disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
confusion; confusion (mental); dementia; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease confusion; confusion (mental); dementia; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease mental disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental illness Gene Set From GAD Gene-Disease Associations genes associated with the disease mental illness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental processes Gene Set From GAD Gene-Disease Associations genes associated with the disease mental processes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental competency Gene Set From GAD Gene-Disease Associations genes associated with the disease mental competency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mental in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
mental depression Gene Set From GWASdb SNP-Disease Associations genes associated with the disease mental depression in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
drug-induced mental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease drug-induced mental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
alcohol-induced mental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease alcohol-induced mental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
developmental disorder of mental health Gene Set From GWASdb SNP-Disease Associations genes associated with the disease developmental disorder of mental health in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
disease of mental health Gene Set From GWASdb SNP-Disease Associations genes associated with the disease disease of mental health in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
mental deterioration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the mental deterioration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of higher mental function Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of higher mental function Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of higher mental function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mental deterioration Gene Set From HPO Gene-Disease Associations genes associated with the mental deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Mental Processes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Processes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Competency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Competency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Health Services Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Health Services phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Fatigue Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Fatigue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Health Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Health phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Community Mental Health Services Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Community Mental Health Services phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Recall Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Recall phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Status Schedule Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Status Schedule phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
MENTAL domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the MENTAL domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
{mental health wellness-1} Gene Set From OMIM Gene-Disease Associations genes associated with the {mental health wellness-1} phenotype from the curated OMIM Gene-Disease Associations dataset.
{mental health wellness-2} Gene Set From OMIM Gene-Disease Associations genes associated with the {mental health wellness-2} phenotype from the curated OMIM Gene-Disease Associations dataset.
Mental Depression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Disorders, Severe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Disorders, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Organic Mental Disorders, Substance-Induced Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Organic Mental Disorders, Substance-Induced in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Status Changes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Status Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Handicap Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Handicap in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Condensation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Condensation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Alcohol-Induced Mental Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Alcohol-Induced Mental Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Organic Mental Disorders, Psychotic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Organic Mental Disorders, Psychotic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mental Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Palmo-Mental Reflex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Palmo-Mental Reflex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Mental State Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Mental State in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Taste Perception (Mental Process) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Taste Perception (Mental Process) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Higher Mental Function Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Higher Mental Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal mental foramen morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mental foramen morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent mental foramen Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent mental foramen phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Disease of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Disease of mental health from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental disorder of mental health from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Disease of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Disease of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Disease of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Disease of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental disorder of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
drug-induced mental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease drug-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
alcohol-induced mental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mental deterioration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mental deterioration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mental development (prenatal lead exposure interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mental development (prenatal lead exposure interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mental health related quality of life Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mental health related quality of life phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pharmacokinetics of antiepileptic drugs in severe mental disorder (concentration drug ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pharmacokinetics of antiepileptic drugs in severe mental disorder (concentration drug ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pharmacokinetics of antipsychotic drugs in severe mental disorder (concentration drug ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pharmacokinetics of antipsychotic drugs in severe mental disorder (concentration drug ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pharmacokinetics of olanzapine in severe mental disorder (concentration dose ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pharmacokinetics of olanzapine in severe mental disorder (concentration dose ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mental health study participation (provided email address) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mental health study participation (provided email address) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mental health study participation (completed survey) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mental health study participation (completed survey) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypoparathyroidism retardation dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoparathyroidism retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoparathyroidism-retardation-dysmorphism syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoparathyroidism-retardation-dysmorphism syndrome from the curated CTD Gene-Disease Associations dataset.
Fetal Growth Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Growth Retardation from the curated CTD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; pre-eclampsia; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intrauterine growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; periodontal diseases; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; periodontal diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; hellp syndrome; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retardation Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term retardation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
mild postnatal growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the mild postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild intrauterine growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the mild intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intrauterine growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe intrauterine growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the severe intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
postnatal growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe postnatal growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the severe postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Fetal Growth Retardation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Growth Retardation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
prenatal growth retardation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the prenatal growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fetal growth retardation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fetal growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
growth retardation of incisors Gene Set From MPO Gene-Phenotype Associations gene mutations causing the growth retardation of incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
growth retardation of molars Gene Set From MPO Gene-Phenotype Associations gene mutations causing the growth retardation of molars phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
postnatal growth retardation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the postnatal growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
embryonic growth retardation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the embryonic growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hypoparathyroidism-retardation-dysmorphism syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the hypoparathyroidism-retardation-dysmorphism syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Chorea, Childhood-Onset, With Psychomotor Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Childhood-Onset, With Psychomotor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypoparathyroidism-Retardation-Dysmorphism Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoparathyroidism-Retardation-Dysmorphism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Motor Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intrauterine Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrauterine Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Postnatal Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postnatal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Postnatal Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Postnatal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Psychomotor Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Psychomotor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Psychomotor Retardation Due To S-Adenosylhomocysteine Hydrolase Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Psychomotor Retardation Due To S-Adenosylhomocysteine Hydrolase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Moderate Intrauterine Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Moderate Intrauterine Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Postnatal Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Postnatal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Intrauterine Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Intrauterine Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Intrauterine Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Intrauterine Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
embryonic growth retardation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic growth retardation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
postnatal growth retardation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the postnatal growth retardation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fetal growth retardation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fetal growth retardation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
growth retardation of molars Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the growth retardation of molars phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
growth retardation of incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the growth retardation of incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prenatal growth retardation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prenatal growth retardation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic growth retardation Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the embryonic growth retardation phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
hypoparathyroidism-retardation-dysmorphism syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypoparathyroidism-retardation-dysmorphism syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypoparathyroidism-retardation-dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypoparathyroidism-retardation-dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Psychomotor retardation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Psychomotor retardation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Postnatal growth retardation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Postnatal growth retardation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intrauterine growth retardation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intrauterine growth retardation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Growth retardation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth retardation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
anterior group of nuclei, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
anterior orbital gyrus, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior orbital gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, anterior region, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, anterior region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
paracentral lobule, anterior part, right, superior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, anterior part, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
paracentral lobule, anterior part, right, inferior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, anterior part, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
paracentral lobule, anterior part, left, inferior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, anterior part, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
paracentral lobule, anterior part, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, anterior part, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
anterior group of nuclei, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, anterior region, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, anterior region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
paracentral lobule, anterior part, left, superior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, anterior part, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
anterior hypothalamic area, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior hypothalamic area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
anterior orbital gyrus, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior orbital gyrus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
anterior hypothalamic area, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior hypothalamic area, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
anterior olfactory area, dorsal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior olfactory area, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior olfactory area, ventral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior olfactory area, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior tegmental nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior tegmental nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, ventral part, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, ventral part, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, dorsal part, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, dorsal part, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
nucleus of the stria terminalis, medial division, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in nucleus of the stria terminalis, medial division, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior paraventricular nucleus of thalamus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior paraventricular nucleus of thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, anterolateral area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, anterolateral area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior pretectal nucleus, ventral core part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior pretectal nucleus, ventral core part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, oval nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, oval nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior nuclei Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior nuclei relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Dorsomedial nucleus of the hypothalamus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Dorsomedial nucleus of the hypothalamus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior olfactory nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior olfactory nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior digastric muscle trigeminal motor cell group Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior digastric muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
interstitial nucleus of the posterior limb of the anterior commissure Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in interstitial nucleus of the posterior limb of the anterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, ventral part, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, ventral part, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, ventral part, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, ventral part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, dorsal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, fusiform nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, fusiform nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, ventral nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, ventral nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior hypothalamic nucleus, central part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, juxtacapsular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, juxtacapsular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, anteromedial area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, anteromedial area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Basolateral amygdalar nucleus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basolateral amygdalar nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior pretectal nucleus, ventral superficial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior pretectal nucleus, ventral superficial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nucleus of the anterior commissure Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nucleus of the anterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior group of the dorsal thalamus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior pretectal nucleus, dorsal superficial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior pretectal nucleus, dorsal superficial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior olfactory nucleus, lateral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior olfactory nucleus, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior pretectal nucleus, dorsal core part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior pretectal nucleus, dorsal core part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
basomedial amygdaloid nucleus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in basomedial amygdaloid nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Ventral anterior-lateral complex of the thalamus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventral anterior-lateral complex of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior amygdalar area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior amygdalar area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior olfactory nucleus, dorsal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior olfactory nucleus, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, dorsal part, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, dorsal part, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior olfactory nucleus, external part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior olfactory nucleus, external part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cortical amygdalar area, anterior part, layer 2 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, anterior part, layer 2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior olfactory nucleus, medial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior olfactory nucleus, medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, rhomboid nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, rhomboid nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, dorsal part, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, dorsal part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
basolateral amygdaloid nucleus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in basolateral amygdaloid nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cortical amygdalar area, anterior part, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, anterior part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Basomedial amygdalar nucleus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basomedial amygdalar nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior olfactory nucleus, posteroventral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior olfactory nucleus, posteroventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior part of Int Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior part of Int relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior hypothalamic nucleus, posterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, ventral part, 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, ventral part, 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, ventral part, 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, ventral part, 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, magnocellular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, magnocellular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cortical amygdalar area, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, ventral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior olfactory nucleus, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior olfactory nucleus, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior pretectal nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior pretectal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, dorsal part, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, dorsal part, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior cingulate area, dorsal part, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior cingulate area, dorsal part, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Bed nuclei of the stria terminalis, anterior division, dorsomedial nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, dorsomedial nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posterior part of anterior hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior part of anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
lateral anterior hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Ventromedial hypothalamic nucleus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventromedial hypothalamic nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior cortical amygdaloid area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior cortical amygdaloid area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_19 yrs_F_12832 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12981 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_11 yrs_F_12289 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_37 pcw_M_263195015 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12890 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
anterior hypothalamic nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
anterior nucleus of pulvinar Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior nucleus of pulvinar relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
anterior cortical nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior cortical nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
ventral anterior nucleus of thalamus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in ventral anterior nucleus of thalamus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
anterior amygdaloid area Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior amygdaloid area relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, anterior part Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, anterior part relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
rostral (anterior) extramural migratory stream Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in rostral (anterior) extramural migratory stream relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Lethal arthrogryposis with anterior horn cell disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anterior segment mesenchymal dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anterior segment mesenchymal dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Myopathy, Distal, with Anterior Tibial Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.
Anterior segment mesenchymal dysgenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anterior segment mesenchymal dysgenesis from the curated CTD Gene-Disease Associations dataset.
Anterior polar cataract 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anterior polar cataract 2 from the curated CTD Gene-Disease Associations dataset.
Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease from the curated CTD Gene-Disease Associations dataset.
anterior spinal artery syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior spinal artery syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior horn cell disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior horn cell disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior compartment syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior compartment syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior cranial fossa meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior cranial fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior uveitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior uveitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior scleritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior scleritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior cerebral artery infarction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
rheumatoid spondylitis; spondylitis, ankylosing; uveitis, anterior Gene Set From GAD Gene-Disease Associations genes associated with the disease rheumatoid spondylitis; spondylitis, ankylosing; uveitis, anterior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
uveitis, anterior Gene Set From GAD Gene-Disease Associations genes associated with the disease uveitis, anterior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute anterior uveitis Gene Set From GAD Gene-Disease Associations genes associated with the disease acute anterior uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene Set From GAD Gene-Disease Associations genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anterior Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term anterior in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
H6PD_KO_GDS3195_603_mouse_Skeletal muscle - Tibialis anterior Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the H6PD_KO_GDS3195_603_mouse_Skeletal muscle - Tibialis anterior gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
positive regulation of anterior head development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of anterior head development biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic heart tube anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior axis specification, embryo Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations 2015 dataset.
specification of ureteric bud anterior/posterior symmetry Gene Set From GO Biological Process Annotations 2015 genes participating in the specification of ureteric bud anterior/posterior symmetry biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior neuropore closure Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior neuropore closure biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior compartment pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior compartment pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
cardioblast anterior-lateral migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cardioblast anterior-lateral migration biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior pattern specification involved in kidney development Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2015 dataset.
canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior commissure morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior commissure morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
polarity specification of anterior/posterior axis Gene Set From GO Biological Process Annotations 2015 genes participating in the polarity specification of anterior/posterior axis biological process from the curated GO Biological Process Annotations 2015 dataset.
specification of anterior mesonephric tubule identity Gene Set From GO Biological Process Annotations 2015 genes participating in the specification of anterior mesonephric tubule identity biological process from the curated GO Biological Process Annotations 2015 dataset.
epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification Gene Set From GO Biological Process Annotations 2015 genes participating in the epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations 2015 dataset.
spemann organizer formation at the anterior end of the primitive streak Gene Set From GO Biological Process Annotations 2015 genes participating in the spemann organizer formation at the anterior end of the primitive streak biological process from the curated GO Biological Process Annotations 2015 dataset.
zygotic determination of anterior/posterior axis, embryo Gene Set From GO Biological Process Annotations 2015 genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior axis specification Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior axis specification biological process from the curated GO Biological Process Annotations 2015 dataset.
fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
neural plate anterior/posterior regionalization Gene Set From GO Biological Process Annotations 2015 genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord anterior/posterior patterning Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of anterior head development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of anterior head development biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior pattern specification involved in ureteric bud development Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification involved in ureteric bud development biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior semicircular canal development Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior semicircular canal development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
forebrain anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the forebrain anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription involved in anterior/posterior axis specification Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations 2015 dataset.
Anterior chamber depth Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Anterior chamber depth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
abnormality of the anterior segment of the eye Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the anterior pituitary Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
anterior polar cataract Gene Set From HPO Gene-Disease Associations genes associated with the anterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior chamber synechiae Gene Set From HPO Gene-Disease Associations genes associated with the anterior chamber synechiae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular ossification at anterior rib ends Gene Set From HPO Gene-Disease Associations genes associated with the irregular ossification at anterior rib ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior beaking of lumbar vertebrae Gene Set From HPO Gene-Disease Associations genes associated with the anterior beaking of lumbar vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior encephalocele Gene Set From HPO Gene-Disease Associations genes associated with the anterior encephalocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the anterior chamber Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
left anterior fascicular block Gene Set From HPO Gene-Disease Associations genes associated with the left anterior fascicular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior tibial bowing Gene Set From HPO Gene-Disease Associations genes associated with the anterior tibial bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior beaking of thoracic vertebrae Gene Set From HPO Gene-Disease Associations genes associated with the anterior beaking of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior rib cupping Gene Set From HPO Gene-Disease Associations genes associated with the anterior rib cupping phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Harmonizome 3.0

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

mental retardation, anterior maxillary protrusion, and strabismus Gene Set

Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene Set

scaphocephaly, maxillary retrusion, and mental retardation Gene Set

growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set

cystic fibrosis; maxillary sinusitis; sinusitis, maxillary Gene Set

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set

Arthrogryposis, mental retardation, and seizures Gene Set

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

Mental retardation with language impairment and autistic features Gene Set

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

Microcephaly with mental retardation and digital anomalies Gene Set

Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

Aniridia, cerebellar ataxia, and mental retardation Gene Set

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

Alacrima, achalasia, and mental retardation syndrome Gene Set

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

Growth deficiency and mental retardation with facial dysmorphism Gene Set

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set

Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set

PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set

Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set

Cleft Palate, Isolated, And Mental Retardation Gene Set

Microcephaly with Mental Retardation and Digital Anomalies Gene Set

Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene Set

Cubitus Valgus with Mental Retardation and Unusual Facies Gene Set

Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set

epilepsy and mental retardation Gene Set

mental retardation, severe, with spasticity and tapetoretinal degeneration Gene Set

cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set

mental retardation with language impairment and autistic features Gene Set

?rolandic epilepsy, mental retardation, and speech dyspraxia Gene Set

skeletal defects, genital hypoplasia, and mental retardation Gene Set

corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia Gene Set

mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set

alacrima, achalasia, and mental retardation syndrome Gene Set

?arthrogryposis, mental retardation, and seizures Gene Set

mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

choroideremia, deafness, and mental retardation Gene Set

cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome Gene Set

cubitus valgus with mental retardation and unusual facies Gene Set

cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set

epilepsy, focal, with speech disorder and with or without mental retardation Gene Set

mental retardation, x-linked 29 and others Gene Set

ichthyosis, spastic quadriplegia, and mental retardation Gene Set

mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) Gene Set

coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set

alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis Gene Set

Alport Syndrome, Mental Retardation, Midface Hypoplasia, And Elliptocytosis Gene Set

Iris Coloboma With Ptosis, Hypertelorism, And Mental Retardation Gene Set

Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures Gene Set

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, And Obesity Syndrome Gene Set

Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave Gene Set