Ichthyosis, spastic quadriplegia, and mental retardation

Clear Filter

Results for "Ichthyosis, spastic quadriplegia, and mental retardation": 1002 gene sets

Name
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.
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.
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
spastic quadriplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic quadriplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive spastic quadriplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic quadriplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Spastic Quadriplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Spastic Quadriplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype 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.
Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set From OMIM Gene-Disease Associations genes associated with the exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated OMIM Gene-Disease Associations dataset.
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa Of Siemens-Like Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa Of Siemens-Like 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
paraparesis, tropical spastic; tropical spastic paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease paraparesis, tropical spastic; tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Quadriplegia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Quadriplegia from the curated CTD Gene-Disease Associations dataset.
quadriplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease quadriplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
episodic quadriplegia Gene Set From HPO Gene-Disease Associations genes associated with the episodic quadriplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Quadriplegia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Quadriplegia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Quadriplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Quadriplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Flaccid Quadriplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flaccid Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Quadriplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Quadriplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 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.
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.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset.
keratosis linearis with ichthyosis congenita and sclerosing keratoderma Gene Set From OMIM Gene-Disease Associations genes associated with the keratosis linearis with ichthyosis congenita and sclerosing keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratosis Linearis With Ichthyosis Congenita And Sclerosing Keratoderma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Keratosis Linearis With Ichthyosis Congenita And Sclerosing Keratoderma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratitis ichthyosis and deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Keratitis ichthyosis and deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
spastic paraplegia, optic atrophy, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
alzheimer disease, type 3, with spastic paraparesis and unusual plaques Gene Set From OMIM Gene-Disease Associations genes associated with the alzheimer disease, type 3, with spastic paraparesis and unusual plaques phenotype from the curated OMIM Gene-Disease Associations dataset.
alzheimer disease, type 3, with spastic paraparesis and apraxia Gene Set From OMIM Gene-Disease Associations genes associated with the alzheimer disease, type 3, with spastic paraparesis and apraxia phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset.
Severe Intellectual Disability And Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Intellectual Disability And Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic tetraplegia, thin corpus callosum, and progressive microcephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic tetraplegia, thin corpus callosum, and progressive microcephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic tetraplegia and axial hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic tetraplegia and axial hypotonia phenotype from the curated ClinVar Gene-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.
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.
X-linked ichthyosis with steryl-sulfatase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked ichthyosis with steryl-sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Triglyceride storage disease with ichthyosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lamellar ichthyosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lamellar ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis prematurity syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis prematurity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis with hypotrichosis, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis with hypotrichosis, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Harlequin type ichthyosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Harlequin type ichthyosis from the curated CTD Gene-Disease Associations dataset.
Lamellar ichthyosis, type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lamellar ichthyosis, type 2 from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Lamellar, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Lamellar, 5 from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis from the curated CTD Gene-Disease Associations dataset.
Ichthyosis Bullosa of Siemens Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis Bullosa of Siemens from the curated CTD Gene-Disease Associations dataset.
Ichthyosis Vulgaris Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis Vulgaris from the curated CTD Gene-Disease Associations dataset.
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 from the curated CTD Gene-Disease Associations dataset.
Ichthyosis follicularis atrichia photophobia syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis follicularis atrichia photophobia syndrome from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Lamellar Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Lamellar from the curated CTD Gene-Disease Associations dataset.
Ichthyosis hystrix, Curth Macklin type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis hystrix, Curth Macklin type from the curated CTD Gene-Disease Associations dataset.
Ichthyosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis from the curated CTD Gene-Disease Associations dataset.
Ichthyosis prematurity syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis prematurity syndrome from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, X-Linked from the curated CTD Gene-Disease Associations dataset.
Lamellar ichthyosis, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lamellar ichthyosis, type 3 from the curated CTD Gene-Disease Associations dataset.
x-linked ichthyosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease x-linked ichthyosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ichthyosis vulgaris Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ichthyosis vulgaris in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ichthyosis Gene Set From GAD Gene-Disease Associations genes associated with the disease ichthyosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ichthyosis vulgaris Gene Set From GAD Gene-Disease Associations genes associated with the disease ichthyosis vulgaris in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatitis, atopic; ichthyosis vulgaris Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, atopic; ichthyosis vulgaris in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ichthyosis, x-linked Gene Set From GAD Gene-Disease Associations genes associated with the disease ichthyosis, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lamellar ichthyosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lamellar ichthyosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatitis, allergic contact; hypersensitivity; hypersensitivity, immediate; ichthyosis vulgaris Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, allergic contact; hypersensitivity; hypersensitivity, immediate; ichthyosis vulgaris in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ichthyosis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term ichthyosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
ichthyosis Gene Set From HPO Gene-Disease Associations genes associated with the ichthyosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Ichthyosis, X-Linked Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ichthyosis, X-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ichthyosis Vulgaris Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ichthyosis Vulgaris phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ichthyosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ichthyosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
ichthyosis, cyclic, with epidermolytic hyperkeratosis Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, cyclic, with epidermolytic hyperkeratosis phenotype from the curated OMIM Gene-Disease Associations dataset.
hystrix-like ichthyosis with deafness Gene Set From OMIM Gene-Disease Associations genes associated with the hystrix-like ichthyosis with deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis vulgaris Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis vulgaris phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis prematurity syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis prematurity syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis histrix, curth-macklin type Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis histrix, curth-macklin type phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 4a Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 4a phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, autosomal recessive 4b (harlequin) Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, autosomal recessive 4b (harlequin) phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis with confetti Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis with confetti phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 6 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 7 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 8 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 9 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 10 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 11 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis bullosa of siemens Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis bullosa of siemens phenotype from the curated OMIM Gene-Disease Associations dataset.
keratitis-ichthyosis-deafness syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the keratitis-ichthyosis-deafness syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
vohwinkel syndrome with ichthyosis Gene Set From OMIM Gene-Disease Associations genes associated with the vohwinkel syndrome with ichthyosis phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) pathway from the Reactome Pathways dataset.
Triglyceride Storage Disease With Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triglyceride Storage Disease With Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Harlequin Type Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Harlequin Type Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Congenita Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Congenita in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lamellar Ichthyosis, Type 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lamellar Ichthyosis, Type 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Bullosa Of Siemens Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Bullosa Of Siemens in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratitis-Ichthyosis-Deafness Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Keratitis-Ichthyosis-Deafness Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Vulgaris Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Vulgaris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bathing Suit Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bathing Suit Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Ichthyosis Vulgaris Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Ichthyosis Vulgaris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Follicularis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Follicularis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Congenital Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Hystrix Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Hystrix in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratinopathic Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Keratinopathic Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Follicular Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Follicular Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Syndromic Recessive X-Linked Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Syndromic Recessive X-Linked Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Ichthyosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS) pathway from the Reactome Pathways 2024 dataset.
Ichthyosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ichthyosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive congenital ichthyosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive congenital ichthyosis 4B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ichthyosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ichthyosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked ichthyosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked ichthyosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ichthyosis vulgaris Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ichthyosis vulgaris in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 4B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 4A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 4A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant keratitis-ichthyosis-deafness syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant keratitis-ichthyosis-deafness syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ichthyosis follicularis-alopecia-photophobia syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ichthyosis follicularis-alopecia-photophobia syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive congenital ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lamellar ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lamellar ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Keratoderma-ichthyosis-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Keratoderma-ichthyosis-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital ichthyosis of skin Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital ichthyosis of skin phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis linearis circumflexa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis linearis circumflexa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis prematurity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis prematurity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis bullosa of Siemens Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis bullosa of Siemens phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Exfoliative ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Exfoliative ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epidermolytic ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epidermolytic ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Annular epidermolytic ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Annular epidermolytic ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant epidermolytic ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant epidermolytic ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis vulgaris Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis vulgaris phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant keratitis-ichthyosis-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal ichthyosis-sclerosing cholangitis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal ichthyosis-sclerosing cholangitis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant ichthyosis vulgaris Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant ichthyosis vulgaris phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive keratitis-ichthyosis-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive keratitis-ichthyosis-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 46, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 46, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 48, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 48, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 4, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 54, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 54, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia, spastic, 4, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia, spastic, 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 5A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 5A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 11, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 11, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 57, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 57, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 72, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 72, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 35 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 35 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 44, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 44, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic ataxia 5, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic ataxia 5, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 72, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 72, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic ataxia Charlevoix-Saguenay type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic ataxia Charlevoix-Saguenay type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 26 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 55, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 55, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 63, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 63, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 31, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 31, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 39 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 56, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 56, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 30, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 30, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 33, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 33, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia, spastic, 2, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia, spastic, 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 45, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 45, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 42, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 42, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 24 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 24 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 20, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 20, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 32, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 32, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 36, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 36, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 34, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 34, X-Linked from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia type 5A, recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia type 5A, recessive from the curated CTD Gene-Disease Associations dataset.
Ataxia, Spastic, 3, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia, Spastic, 3, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 7, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 7, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Hereditary spastic paralysis, infantile onset ascending Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 4, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 4, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia type 5B, recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia type 5B, recessive from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 31, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 31, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 16, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 16, X-linked from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 42, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 42, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 33, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 33, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 17 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 17 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 11, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 11, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 10, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 10, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 44, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 44, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 2, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 2, X-linked from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 25, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 25, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Paraparesis, Spastic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Paraparesis, Spastic from the curated CTD Gene-Disease Associations dataset.
SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 15, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 15, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 2 from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 39, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 39, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 9, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 9, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 37, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 37, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia-50, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia-50, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 3, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 3, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 38, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 38, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic ataxia Charlevoix-Saguenay type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic ataxia Charlevoix-Saguenay type from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 23 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 23 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 14, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 14, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 29, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 29, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 6, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 6, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 8, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 8, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Ataxia, Spastic, 1, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia, Spastic, 1, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Hereditary from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 27, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 27, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 1 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 13, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 13, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 19, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 19, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 18, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 18, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
hereditary spastic paraplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary spastic paraplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
spastic hemiplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic hemiplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic entropion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic entropion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic diplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic diplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary spastic paraplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary spastic paraplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic ectropion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic ectropion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tropical spastic paraparesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tropical spastic paraparesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
motor neuron disease; paraparesis, spastic Gene Set From GAD Gene-Disease Associations genes associated with the disease motor neuron disease; paraparesis, spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spastic paraplegia Gene Set From GAD Gene-Disease Associations genes associated with the disease spastic paraplegia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spastic paralysis Gene Set From GAD Gene-Disease Associations genes associated with the disease spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary spastic paraparesis due to a frame shift mutat Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-1 associated myelopathy/tropical spastic; paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-1 associated myelopathy/tropical spastic; paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary spastic angina. Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary spastic angina. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary spastic angina Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary spastic angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelopathy/tropical spastic paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease myelopathy/tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spastic paraplegia, hereditary Gene Set From GAD Gene-Disease Associations genes associated with the disease spastic paraplegia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile-onset ascending hereditary spastic paralysis Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; spastic paraplegia, hereditary Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; spastic paraplegia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-i infections; paraparesis, tropical spastic Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i infections; paraparesis, tropical spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spastic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term spastic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
spastic dysarthria Gene Set From HPO Gene-Disease Associations genes associated with the spastic dysarthria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic ataxia Gene Set From HPO Gene-Disease Associations genes associated with the spastic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spastic paraplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic paraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic tetraplegia Gene Set From HPO Gene-Disease Associations genes associated with the spastic tetraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic tetraparesis Gene Set From HPO Gene-Disease Associations genes associated with the spastic tetraparesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic diplegia Gene Set From HPO Gene-Disease Associations genes associated with the spastic diplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic gait Gene Set From HPO Gene-Disease Associations genes associated with the spastic gait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic paraparesis Gene Set From HPO Gene-Disease Associations genes associated with the spastic paraparesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic paraplegia Gene Set From HPO Gene-Disease Associations genes associated with the spastic paraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Paraparesis, Tropical Spastic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paraparesis, Tropical Spastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Paraparesis, Spastic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paraparesis, Spastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spastic Paraplegia, Hereditary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spastic Paraplegia, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
spastic paraplegia 8, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 8, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 13, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 13, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 5a, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 5a, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 12, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 12, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 72, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 72, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 29, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 29, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 16, x-linked, complicated Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 16, x-linked, complicated phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 18, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 18, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, with spastic paraplegia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, with spastic paraplegia phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 32, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 32, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 53, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 53, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 19, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 19, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 3, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 3, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 33, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 33, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 64 Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 64 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 30, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 30, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 42, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 42, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 43, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 43, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 45, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 45, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 25, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 25, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 39, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 39, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 55, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 55, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 24, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 24, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 28, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 28, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 37, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 11, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 11, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 2, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 46, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 46, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 38, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 38, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 26, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 26, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 51, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 51, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 47, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 47, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 27, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 27, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 9, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 9, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 34, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 34, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 52, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 52, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 14, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 14, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 56, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 56, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 35, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 35, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 10, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 10, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 41, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 41, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral palsy, spastic quadriplegic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral palsy, spastic quadriplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 50, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 50, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 44, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 44, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 63 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 63 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 15, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 15, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 36, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 36, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 72, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 72, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 49, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 49, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 7, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 7, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 3a, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 3a, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 54, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 54, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
silver spastic paraplegia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the silver spastic paraplegia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, spastic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, spastic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, spastic, 5, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, spastic, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 61, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 61, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 48, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 48, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 57, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 57, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral palsy, spastic quadriplegic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral palsy, spastic quadriplegic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 45 Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 45 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 31, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 31, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia, charlevoix-saguenay type Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia, charlevoix-saguenay type phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paralysis, infantile onset ascending Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) pathway from the Reactome Pathways dataset.
Spastic Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Functional Diarrhoea (Due To Spastic Colon) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Functional Diarrhoea (Due To Spastic Colon) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Tetraparesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Tetraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tropical Spastic Paraparesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tropical Spastic Paraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Palsy, Spastic Quadriplegic, 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Hereditary Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complicated Hereditary Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complicated Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Autosomal Dominant Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Autosomal Dominant Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Spastic Paralysis, Infantile Onset Ascending Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Spastic Paralysis, Infantile Onset Ascending in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pure Hereditary Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pure Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Diplegia Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Diplegia Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mt-Atp6-Related Mitochondrial Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mt-Atp6-Related Mitochondrial Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary X-Linked Recessive Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary X-Linked Recessive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked, Spastic Paraplegia, Hereditary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked, Spastic Paraplegia, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraparesis, Spastic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paraparesis, Spastic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spastic Gait Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spastic Gait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraparesis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Coronary Spastic Angina Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Coronary Spastic Angina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spastic/Hyperactive Bladder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spastic/Hyperactive Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spastic Paraparetic Gait Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spastic Paraparetic Gait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spastic Paraplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC33A1 causes spastic paraplegia 42 (SPG42) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC33A1 causes spastic paraplegia 42 (SPG42) pathway from the Reactome Pathways 2024 dataset.
Hereditary spastic paraplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 31 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 31 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 15 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 15 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Charlevoix-Saguenay spastic ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 35 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 35 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 7 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 7 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 3A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 3A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 5A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 5A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 8 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 8 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 11 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 11 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 49 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 49 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 17 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 17 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic quadriplegic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic quadriplegic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tropical spastic paraparesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tropical spastic paraparesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 61 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 61 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 73 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 73 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 39 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 39 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic diplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic diplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 76 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 76 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 49 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 49 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 81 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 81 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 78 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 78 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic hemiplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic hemiplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 75 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 75 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 9A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 9A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 63 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 63 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 45 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 77 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 77 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 70 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 70 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 5A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 5A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 64 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 64 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 47 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 3A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charlevoix-Saguenay spastic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 84 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 84 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 57 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 57 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic entropion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic entropion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 51 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic monoplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic monoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 72A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 72A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 87 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 87 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 9B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 9B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 82 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 82 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic quadriplegic cerebral palsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic quadriplegic cerebral palsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 85 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 85 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraparesis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraparesis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charlevoix-Saguenay spastic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-progressive spastic diplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-progressive spastic diplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

ichthyosis, spastic quadriplegia, and mental retardation Gene Set

Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Gene Set

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

spastic quadriplegia Gene Set

progressive spastic quadriplegia Gene Set

Spastic Quadriplegia Gene Set

Progressive Spastic Quadriplegia 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

Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set

exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set

Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa Of Siemens-Like Gene Set

Arthrogryposis, mental retardation, and seizures Gene Set

Mental retardation with language impairment and autistic features Gene Set

Mental retardation, anterior maxillary protrusion, and strabismus 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

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS 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

Scaphocephaly, Maxillary Retrusion, And Mental Retardation 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

mental retardation, anterior maxillary protrusion, and strabismus 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

scaphocephaly, maxillary retrusion, and mental retardation 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

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