Neonatal short-limb short stature

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Results for "Neonatal short-limb short stature": 867 gene sets

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neonatal short-limb short stature Gene Set From HPO Gene-Disease Associations genes associated with the neonatal short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Neonatal Short-Limb Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
neonatal short-trunk short stature Gene Set From HPO Gene-Disease Associations genes associated with the neonatal short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Neonatal Short-Trunk Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
childhood-onset short-trunk short stature Gene Set From HPO Gene-Disease Associations genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
disproportionate short-trunk short stature Gene Set From HPO Gene-Disease Associations genes associated with the disproportionate short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lethal short-limbed short stature Gene Set From HPO Gene-Disease Associations genes associated with the lethal short-limbed short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Lethal Short-Limbed Short Stature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lethal Short-Limbed Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood-Onset Short-Trunk Short Stature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disproportionate Short-Trunk Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disproportionate Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infancy Onset Short-Trunk Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infancy Onset Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Short stature, idiopathic, autosomal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia/short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, idiopathic, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, short stature, and impaired glucose metabolism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Yakut short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Yakut short stature syndrome 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.
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS 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.
Short Stature, Idiopathic, Autosomal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, Autosomal from the curated CTD Gene-Disease Associations dataset.
Short Stature, Idiopathic, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, X-Linked from the curated CTD Gene-Disease Associations dataset.
short stature Gene Set From GAD Gene-Disease Associations genes associated with the disease short stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic short stature Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic short stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
moderately short stature Gene Set From HPO Gene-Disease Associations genes associated with the moderately short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short stature Gene Set From HPO Gene-Disease Associations genes associated with the short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mesomelic short stature Gene Set From HPO Gene-Disease Associations genes associated with the mesomelic short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
disproportionate short stature Gene Set From HPO Gene-Disease Associations genes associated with the disproportionate short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild short stature Gene Set From HPO Gene-Disease Associations genes associated with the mild short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proportionate short stature Gene Set From HPO Gene-Disease Associations genes associated with the proportionate short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe short stature Gene Set From HPO Gene-Disease Associations genes associated with the severe short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia/short stature syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia/short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature Gene Set From OMIM Gene-Disease Associations genes associated with the short stature phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature 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.
microcephaly, short stature, and impaired glucose metabolism Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, short stature, and impaired glucose metabolism phenotype from the curated OMIM Gene-Disease Associations dataset.
osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene Set From OMIM Gene-Disease Associations genes associated with the osteochondritis dissecans, short stature, and early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature with microcephaly and distinctive facies Gene Set From OMIM Gene-Disease Associations genes associated with the short stature with microcephaly and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, idiopathic familial Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From OMIM Gene-Disease Associations genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.
Ear, Patella, Short Stature Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ear, Patella, Short Stature Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Stature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Stature Homeobox Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Stature Homeobox Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pituitary Short Stature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pituitary Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Stature, Idiopathic, Autosomal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Stature, Idiopathic, Autosomal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Joint Laxity, Short Stature, And Myopia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Joint Laxity, Short Stature, And Myopia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facial Dysmorphism, Immunodeficiency, Livedo, And Short Stature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facial Dysmorphism, Immunodeficiency, Livedo, And Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Shox-Related Short Stature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Shox-Related Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Stature, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Stature, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Disproportionate Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disproportionate Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proportionate Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proportionate Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Moderately Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Moderately Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Stature, Postnatal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Stature, Postnatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mesomelic Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mesomelic Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intellectual developmental disorder with short stature and behavioral abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with short stature and behavioral abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short stature, hearing loss, retinitis pigmentosa, and distinctive facies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short stature, hearing loss, retinitis pigmentosa, and distinctive facies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual disability-short stature-overweight syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual disability-short stature-overweight syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
SHOX-related short stature Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease SHOX-related short stature in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short stature Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature due to growth hormone secretagogue receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to growth hormone secretagogue receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature due to partial GHR deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to partial GHR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SHOX-related short stature Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SHOX-related short stature phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature and advanced bone age Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature and advanced bone age phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature due to growth hormone qualitative anomaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to growth hormone qualitative anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-optic atrophy-Pelger-Huet anomaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-optic atrophy-Pelger-Huet anomaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Facial dysmorphism-immunodeficiency-livedo-short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Facial dysmorphism-immunodeficiency-livedo-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-pituitary and cerebellar defects-small sella turcica syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-pituitary and cerebellar defects-small sella turcica syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-brachydactyly-obesity-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-brachydactyly-obesity-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability-short stature-overweight syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability-short stature-overweight syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature due to primary acid-labile subunit deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to primary acid-labile subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proportionate short stature Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proportionate short stature phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature and microcephaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature and microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
First year height change in growth hormone-treated short stature Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the First year height change in growth hormone-treated short stature phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Camptodactyly, tall stature, and hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
heritability of stature Gene Set From GAD Gene-Disease Associations genes associated with the disease heritability of stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth height growth to adolescence and adult stature Gene Set From GAD Gene-Disease Associations genes associated with the disease birth height growth to adolescence and adult stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stature among african pygmies Gene Set From GAD Gene-Disease Associations genes associated with the disease stature among african pygmies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
testosterone; bone density; stature Gene Set From GAD Gene-Disease Associations genes associated with the disease testosterone; bone density; stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stature Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term stature in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
disproportionate tall stature Gene Set From HPO Gene-Disease Associations genes associated with the disproportionate tall stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tall stature Gene Set From HPO Gene-Disease Associations genes associated with the tall stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
{stature qtl 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 17} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 17} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 15} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 15} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 13} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 13} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 11} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 11} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 23} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 23} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 21} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 21} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 7} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 7} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 16} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 16} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 14} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 14} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 19} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 19} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 18} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 18} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 22} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 22} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 20} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 20} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stature qtl 24} Gene Set From OMIM Gene-Disease Associations genes associated with the {stature qtl 24} phenotype from the curated OMIM Gene-Disease Associations dataset.
Tall Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tall Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Disproportionate Tall Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disproportionate Tall Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proportionate Tall Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proportionate Tall Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
camptodactyly-tall stature-scoliosis-hearing loss syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease camptodactyly-tall stature-scoliosis-hearing loss syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Camptodactyly-tall stature-scoliosis-hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Camptodactyly-tall stature-scoliosis-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Disproportionate tall stature Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Disproportionate tall stature phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Tall stature-scoliosis-macrodactyly of the great toes syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Tall stature-scoliosis-macrodactyly of the great toes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Tall stature-intellectual disability-renal anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Tall stature-intellectual disability-renal anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Tall stature Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Tall stature phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transient neonatal diabetes mellitus 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Transient neonatal diabetes mellitus 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal insulin-dependent diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal insulin-dependent diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperparathyroidism, neonatal severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperparathyroidism, neonatal severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus, permanent neonatal, with neurologic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus, permanent neonatal, with neurologic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal adrenoleucodystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal adrenoleucodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Permanent neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Permanent neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal intrahepatic cholestasis caused by citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal intrahepatic cholestasis caused by citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus, permanent neonatal, with cerebellar agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus, permanent neonatal, with cerebellar agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cyanosis, transient neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cyanosis, transient neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal from the curated CTD Gene-Disease Associations dataset.
Hyperparathyroidism, Neonatal Severe Primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperparathyroidism, Neonatal Severe Primary from the curated CTD Gene-Disease Associations dataset.
Neonatal-onset citrullinemia type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neonatal-onset citrullinemia type 2 from the curated CTD Gene-Disease Associations dataset.
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Jaundice, Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jaundice, Neonatal from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 3 from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 1 from the curated CTD Gene-Disease Associations dataset.
Finnish lethal neonatal metabolic syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Finnish lethal neonatal metabolic syndrome from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 2 from the curated CTD Gene-Disease Associations dataset.
Pancreatic beta cell agenesis with neonatal diabetes mellitus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pancreatic beta cell agenesis with neonatal diabetes mellitus from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.
Hyperbilirubinemia, Transient Familial Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Permanent Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal from the curated CTD Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neonatal Abstinence Syndrome from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Benign Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Benign Neonatal from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Benign Neonatal, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Benign Neonatal, 3 from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.
Anemia, Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Neonatal from the curated CTD Gene-Disease Associations dataset.
Thrombocytopenia, Neonatal Alloimmune Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Neonatal Alloimmune from the curated CTD Gene-Disease Associations dataset.
neonatal period electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease neonatal period electroclinical syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
neonatal candidiasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal candidiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
transient neonatal neutropenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transient neonatal neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal jaundice Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal jaundice in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal period electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal period electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal thyrotoxicosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal thyrotoxicosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal abstinence syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal abstinence syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal myasthenia gravis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal myasthenia gravis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal respiratory failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal respiratory failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
transient neonatal thrombocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transient neonatal thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glucosephosphate dehydrogenase deficiency; hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set From GAD Gene-Disease Associations genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal thrombocytopenia Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; respiratory distress syndrome, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
respiratory distress syndrome, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal infection Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal hyperbilirubinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal hyperbilirubinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperbilirubinemia, neonatal; jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperbilirubinemia, neonatal; jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cutaneous neonatal lupus Gene Set From GAD Gene-Disease Associations genes associated with the disease cutaneous neonatal lupus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jaundice, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease jaundice, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute neonatal disease and hyperammonemia Gene Set From GAD Gene-Disease Associations genes associated with the disease acute neonatal disease and hyperammonemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term neonatal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
KDM4C_natural variation_GSE41040_589_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_589_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
KDM4C_natural variation_GSE41040_588_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_588_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
KDM4C_natural variation_GSE41040_590_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_590_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
Neonatal lupus Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Neonatal lupus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
neonatal unconjugated hyperbilirubinemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal unconjugated hyperbilirubinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal hyperbilirubinemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hyperbilirubinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal breathing dysregulation Gene Set From HPO Gene-Disease Associations genes associated with the neonatal breathing dysregulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal alloimmune thrombocytopenia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal alloimmune thrombocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal epiphyseal stippling Gene Set From HPO Gene-Disease Associations genes associated with the neonatal epiphyseal stippling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal death Gene Set From HPO Gene-Disease Associations genes associated with the neonatal death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal insulin-dependent diabetes mellitus Gene Set From HPO Gene-Disease Associations genes associated with the neonatal insulin-dependent diabetes mellitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal wrinkled skin of hands and feet Gene Set From HPO Gene-Disease Associations genes associated with the neonatal wrinkled skin of hands and feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized neonatal hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spontaneous neonatal pneumothorax Gene Set From HPO Gene-Disease Associations genes associated with the spontaneous neonatal pneumothorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal respiratory distress Gene Set From HPO Gene-Disease Associations genes associated with the neonatal respiratory distress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
transient neonatal diabetes mellitus Gene Set From HPO Gene-Disease Associations genes associated with the transient neonatal diabetes mellitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prolonged neonatal jaundice Gene Set From HPO Gene-Disease Associations genes associated with the prolonged neonatal jaundice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal hypoglycemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal onset Gene Set From HPO Gene-Disease Associations genes associated with the neonatal onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neonatal Abstinence Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Jaundice, Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Jaundice, Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Benign Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Benign Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hyperbilirubinemia, Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperbilirubinemia, Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Thrombocytopenia, Neonatal Alloimmune Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Thrombocytopenia, Neonatal Alloimmune phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
partial neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
diabetes mellitus, neonatal, with congenital hypothyroidism Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, neonatal, with congenital hypothyroidism phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperparathyroidism, neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
?diabetes mellitus, insulin-dependent, neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the ?diabetes mellitus, insulin-dependent, neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal 2 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, neonatal hemolytic, fatal and near-fatal Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, neonatal hemolytic, fatal and near-fatal phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombocytopenia, neonatal alloimmune Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenia, neonatal alloimmune phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, permanent neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, permanent neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperbilirubinemia, familial transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperbilirubinemia, familial transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia gravis, neonatal transient Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia gravis, neonatal transient phenotype from the curated OMIM Gene-Disease Associations dataset.
cpt ii deficiency, lethal neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the cpt ii deficiency, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
{diabetes mellitus, transient neonatal} Gene Set From OMIM Gene-Disease Associations genes associated with the {diabetes mellitus, transient neonatal} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, neonatal alloimmune Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, neonatal alloimmune phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, neonatal severe Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, neonatal severe phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombocytopenia, neonatal alloimmune, bak antigen related Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenia, neonatal alloimmune, bak antigen related phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes, permanent neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes, permanent neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
citrullinemia, type ii, neonatal-onset Gene Set From OMIM Gene-Disease Associations genes associated with the citrullinemia, type ii, neonatal-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, permanent neonatal, with neurologic features Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, permanent neonatal, with neurologic features phenotype from the curated OMIM Gene-Disease Associations dataset.
choreoathetosis, hypothyroidism, and neonatal respiratory distress Gene Set From OMIM Gene-Disease Associations genes associated with the choreoathetosis, hypothyroidism, and neonatal respiratory distress phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypertrypsinemia, neonatal} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypertrypsinemia, neonatal} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, alloimmune neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, alloimmune neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary hypertension, neonatal, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, neonatal, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
zinc deficiency, transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the zinc deficiency, transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
cyanosis, transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the cyanosis, transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
neonatal Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term neonatal in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Neonatal Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Respiratory Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Abstinence Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hepatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay, Epilepsy, And Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Delay, Epilepsy, And Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
K Atp Permanent Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease K Atp Permanent Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypoglycemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypoglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adrenoleukodystrophy, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adrenoleukodystrophy, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Alloimmune Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Alloimmune Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Cholangitis, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Cholangitis, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Herpes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Herpes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Opiate Withdrawal Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Opiate Withdrawal Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Deformity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypoxic Ischemic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypoxic Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Inflammatory Skin And Bowel Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Inflammatory Skin And Bowel Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Citrullinemia, Type Ii, Neonatal-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Citrullinemia, Type Ii, Neonatal-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hemochromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hemochromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypocalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypocalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Systemic Lupus Erythematosus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Systemic Lupus Erythematosus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Renal Tubular Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Chlamydial Conjunctivitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Chlamydial Conjunctivitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Early-Onset Sepsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Early-Onset Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alloimmune Neonatal Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alloimmune Neonatal Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thrombocytopenia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thrombocytopenia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Meningitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperglycemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Onset Neonatal Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Onset Neonatal Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Late-Onset Sepsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Late-Onset Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Torulopsis Glabrata Fungemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Torulopsis Glabrata Fungemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Marfan Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Marfan Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Diarrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Intestinal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Noninfective Neonatal Diarrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Noninfective Neonatal Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Necrotizing Enterocolitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Necrotizing Enterocolitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Respiratory System Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Respiratory System Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Leukaemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Leukaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Hypothyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cyanosis, Transient Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cyanosis, Transient Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Indirect Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Indirect Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Alloimmune Thrombocytopenia (Nait) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Alloimmune Thrombocytopenia (Nait) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Maladjustment Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Maladjustment Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy, Nonfamilial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy, Nonfamilial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Listeriosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Listeriosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thrombosis Of Cerebral Venous Sinus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thrombosis Of Cerebral Venous Sinus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Unconjugated Hyperbilirubinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Unconjugated Hyperbilirubinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
6Q24-Related Transient Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 6Q24-Related Transient Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Testicular Torsion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Testicular Torsion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Laryngospasm, Severe Neonatal Episodic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Laryngospasm, Severe Neonatal Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Disorder Of Endocrine System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Disorder Of Endocrine System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperthyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperthyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thyrotoxicosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thyrotoxicosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prolonged Neonatal Jaundice Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged Neonatal Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Respiratory Distress Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Respiratory Distress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Insulin-Dependent Diabetes Mellitus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Insulin-Dependent Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Jaundice Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Onset Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tremor, Neonatal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tremor, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spontaneous Neonatal Pneumothorax Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous Neonatal Pneumothorax in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Neonatal Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Neonatal Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Breathing Dysregulation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Breathing Dysregulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Cholestatic Liver Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Cholestatic Liver Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Wrinkled Skin Of Hands And Feet Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Wrinkled Skin Of Hands And Feet in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypertrypsinemia, Neonatal, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypertrypsinemia, Neonatal, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Direct Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Direct Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Inspiratory Stridor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Inspiratory Stridor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Epiphyseal Stippling Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Epiphyseal Stippling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Transient Neonatal Hyperparathyroidism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Transient Neonatal Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
neonatal lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neonatal lethality, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neonatal lethality Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Neonatal astrocyte_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neonatal astrocyte_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Benign neonatal seizures Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign neonatal seizures from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal period electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neonatal period electroclinical syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal diabetes Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neonatal diabetes from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Permanent neonatal diabetes mellitus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal diabetes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal diabetes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal respiratory failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal respiratory failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Permanent neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal jaundice Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal jaundice in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal period electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal period electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
neonatal-onset type II citrullinemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease neonatal-onset type II citrullinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal abstinence syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal abstinence syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal thyrotoxicosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal thyrotoxicosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient neonatal thrombocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient neonatal neutropenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal myasthenia gravis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal myasthenia gravis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal candidiasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal candidiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal diabetes mellitus with congenital hypothyroidism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal diabetes mellitus with congenital hypothyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal infective mastitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal infective mastitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal intrahepatic cholestasis due to citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal intrahepatic cholestasis due to citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal/infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal/infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal severe primary hyperparathyroidism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal severe primary hyperparathyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Permanent neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal insulin-dependent diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal insulin-dependent diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transitory neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transitory neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transient Neonatal Diabetes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transient Neonatal Diabetes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
History of neonatal hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the History of neonatal hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal Marfan syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal Marfan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign neonatal seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign neonatal seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign Neonatal Epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign Neonatal Epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal pseudo-hydrocephalic progeroid syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal pseudo-hydrocephalic progeroid syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal hypoglycemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal hypoglycemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated neonatal sclerosing cholangitis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated neonatal sclerosing cholangitis 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.
Neonatal seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal and neonatal alloimmune thrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal and neonatal alloimmune thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal respiratory distress Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal respiratory distress phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal inflammatory skin and bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal inflammatory skin and bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal white matter microstructure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal white matter microstructure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal cytokine/chemokine levels (maternal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal cytokine/chemokine levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal lupus Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal lupus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
short insular gyri, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in short insular gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
short insular gyri, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in short insular gyri, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Short rib-polydactyly syndrome, Majewski type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-sleeper Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-sleeper phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
short QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the short QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital short bowel syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib polydactyly syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib polydactyly syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
SHORT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the SHORT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brachyrachia (short spine dysplasia) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brachyrachia (short spine dysplasia) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
short-chain collagen trimer Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the short-chain collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
short-chain collagen trimer Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the short-chain collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Short QT Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short QT Syndrome 1 from the curated CTD Gene-Disease Associations dataset.
Short QT Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short QT Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Short QT Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short QT Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Short Rib-Polydactyly Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Rib-Polydactyly Syndrome from the curated CTD Gene-Disease Associations dataset.
Short chain Acyl CoA dehydrogenase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short chain Acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.
Memory, Short-Term Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Memory, Short-Term in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
short bowel syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease short bowel syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
memory, short-term Gene Set From GAD Gene-Disease Associations genes associated with the disease memory, short-term in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; short bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; short bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
short-term response to haloperidol treatment Gene Set From GAD Gene-Disease Associations genes associated with the disease short-term response to haloperidol treatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
short Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term short in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
16478745-SuppTable1-short Gene Set From GeneSigDB Published Gene Signatures genes in signature reported in the publication with PubMedID 16478745-SuppTable1-short from the GeneSigDB Published Gene Signatures dataset.
short-chain fatty acid metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of short-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset.
short-chain fatty acid transport Gene Set From GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset.
short-chain fatty acid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
short-chain fatty acid import Gene Set From GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid import biological process from the curated GO Biological Process Annotations 2015 dataset.
short-term memory Gene Set From GO Biological Process Annotations 2015 genes participating in the short-term memory biological process from the curated GO Biological Process Annotations 2015 dataset.
short-chain fatty acid catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
short-chain collagen trimer Gene Set From GO Cellular Component Annotations 2015 proteins localized to the short-chain collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.
short-chain fatty acid uptake transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the short-chain fatty acid uptake transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
short-chain carboxylesterase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the short-chain carboxylesterase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
short-chain fatty acid transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the short-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Hypertension risk in short sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
short attention span Gene Set From GWASdb SNP-Phenotype Associations genes associated with the short attention span phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
short distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short nasal bridge Gene Set From HPO Gene-Disease Associations genes associated with the short nasal bridge phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short chordae tendineae of the tricuspid valve Gene Set From HPO Gene-Disease Associations genes associated with the short chordae tendineae of the tricuspid valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short nose Gene Set From HPO Gene-Disease Associations genes associated with the short nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the short 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 5th toe Gene Set From HPO Gene-Disease Associations genes associated with the short 5th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 4th toe Gene Set From HPO Gene-Disease Associations genes associated with the short 4th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short diaphyses Gene Set From HPO Gene-Disease Associations genes associated with the short diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short metacarpals with rounded proximal ends Gene Set From HPO Gene-Disease Associations genes associated with the short metacarpals with rounded proximal ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 1st metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the short 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short femoral neck Gene Set From HPO Gene-Disease Associations genes associated with the short femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short digit Gene Set From HPO Gene-Disease Associations genes associated with the short digit phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
relatively short spine Gene Set From HPO Gene-Disease Associations genes associated with the relatively short spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short sacroiliac notch Gene Set From HPO Gene-Disease Associations genes associated with the short sacroiliac notch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short chordae tendineae of the mitral valve Gene Set From HPO Gene-Disease Associations genes associated with the short chordae tendineae of the mitral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short columella Gene Set From HPO Gene-Disease Associations genes associated with the short columella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short nail Gene Set From HPO Gene-Disease Associations genes associated with the short nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short fourth metatarsal Gene Set From HPO Gene-Disease Associations genes associated with the short fourth metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short humerus Gene Set From HPO Gene-Disease Associations genes associated with the short humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short middle phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short philtrum Gene Set From HPO Gene-Disease Associations genes associated with the short philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short metatarsal Gene Set From HPO Gene-Disease Associations genes associated with the short metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short umbilical cord Gene Set From HPO Gene-Disease Associations genes associated with the short umbilical cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short upper lip Gene Set From HPO Gene-Disease Associations genes associated with the short upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short palpebral fissure Gene Set From HPO Gene-Disease Associations genes associated with the short palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short femur Gene Set From HPO Gene-Disease Associations genes associated with the short femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the short phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short attention span Gene Set From HPO Gene-Disease Associations genes associated with the short attention span phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 5th metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the short 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the short middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short chin Gene Set From HPO Gene-Disease Associations genes associated with the short chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short thorax Gene Set From HPO Gene-Disease Associations genes associated with the short thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short mandibular rami Gene Set From HPO Gene-Disease Associations genes associated with the short mandibular rami phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short lingual frenulum Gene Set From HPO Gene-Disease Associations genes associated with the short lingual frenulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 3rd metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the short 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short palm Gene Set From HPO Gene-Disease Associations genes associated with the short palm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short mandibular condyles Gene Set From HPO Gene-Disease Associations genes associated with the short mandibular condyles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 2nd toe Gene Set From HPO Gene-Disease Associations genes associated with the short 2nd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of thumb Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short neck Gene Set From HPO Gene-Disease Associations genes associated with the short neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short foot Gene Set From HPO Gene-Disease Associations genes associated with the short foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short ribs Gene Set From HPO Gene-Disease Associations genes associated with the short ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of hallux Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the short 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short ear Gene Set From HPO Gene-Disease Associations genes associated with the short ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short toe Gene Set From HPO Gene-Disease Associations genes associated with the short toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short thumb Gene Set From HPO Gene-Disease Associations genes associated with the short thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short iliac bones Gene Set From HPO Gene-Disease Associations genes associated with the short iliac bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short lower limbs Gene Set From HPO Gene-Disease Associations genes associated with the short lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short phalanx of hallux Gene Set From HPO Gene-Disease Associations genes associated with the short phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short hard palate Gene Set From HPO Gene-Disease Associations genes associated with the short hard palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short nasal septum Gene Set From HPO Gene-Disease Associations genes associated with the short nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the short metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short long bone Gene Set From HPO Gene-Disease Associations genes associated with the short long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short sternum Gene Set From HPO Gene-Disease Associations genes associated with the short sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the short 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short stepped shuffling gait Gene Set From HPO Gene-Disease Associations genes associated with the short stepped shuffling gait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short tibia Gene Set From HPO Gene-Disease Associations genes associated with the short tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the short 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short 4th metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the short 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short tubular bones (hand) Gene Set From HPO Gene-Disease Associations genes associated with the short tubular bones (hand) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short clavicles Gene Set From HPO Gene-Disease Associations genes associated with the short clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short middle phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the short middle phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short first metatarsal Gene Set From HPO Gene-Disease Associations genes associated with the short first metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short finger Gene Set From HPO Gene-Disease Associations genes associated with the short finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short hallux Gene Set From HPO Gene-Disease Associations genes associated with the short hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Short Bowel Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Short Bowel Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Memory, Short-Term Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Memory, Short-Term phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Short hematopoietin receptor, family 1, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Short hematopoietin receptor, family 1, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Short hematopoietin receptor, family 2, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Short hematopoietin receptor, family 2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Short-chain dehydrogenase/reductase, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Short-chain dehydrogenase/reductase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Short-chain dehydrogenase/reductase SDR Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Short-chain dehydrogenase/reductase SDR protein domain from the InterPro Predicted Protein Domain Annotations dataset.
short nasal bone Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short frontal bone Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short frontal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short perineum Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short perineum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short tail Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short tail phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short photoreceptor inner segment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short squamosal bone Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short squamosal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short malleus manubrium Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short malleus manubrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short metestrus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short metestrus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short metatarsal bones Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short metatarsal bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short diestrus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short diestrus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short photoreceptor outer segment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short vertebral body Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short zygomatic bone Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short zygomatic bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short fibula Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short fibula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short premaxilla Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short premaxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short excitatory postsynaptic current decay time Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short excitatory postsynaptic current decay time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short proestrus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short proestrus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short ureter Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short ureter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short humerus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short humerus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short uterine horn Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short uterine horn phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal short term object recognition memory Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal short term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short tibia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short tibia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short radius Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short radius phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short ulna Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short ulna phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short stride length Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short stride length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short vibrissae Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short vibrissae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short umbilical cord Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short umbilical cord phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short malleus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short malleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short hair Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short lumbar vertebrae Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short lumbar vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short estrous cycle Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short mandible Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short mandible phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short rostral-caudal axis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short cochlear hair cell stereocilia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short maxilla Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short maxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short kidney papilla Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short kidney papilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short outer hair cell stereocilia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short endolymphatic duct Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short oviduct Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short oviduct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short presphenoid bone Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short presphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short ribs Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short ribs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short snout Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short snout phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short vertebral column Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short vertebral column phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short nails Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short nails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short cochlear outer hair cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short gestation period Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short gestation period phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short sternum Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short sternum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal short term spatial reference memory Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal short term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short neck Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short neck phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short femur Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short inner hair cell stereocilia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short sperm flagellum Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short sperm flagellum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short limbs Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short limbs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short metacarpal bones Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short metacarpal bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short incisors Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short scapula Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short scapula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short scala media Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short scala media phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short trachea Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short trachea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short estrus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short estrus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the short syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 4 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
[short sleeper] Gene Set From OMIM Gene-Disease Associations genes associated with the [short sleeper] phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 6 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 7 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital short bowel syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the congenital short bowel syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
short qt syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the short qt syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
short qt syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the short qt syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
short qt syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the short qt syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
acyl-coa dehydrogenase, short-chain, deficiency of Gene Set From OMIM Gene-Disease Associations genes associated with the acyl-coa dehydrogenase, short-chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 3 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 8 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 2 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 5 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
Short Segment Hirschsprung'S Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Segment Hirschsprung'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Corpus Callosum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short-Term Memory Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short-Term Memory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Sleeper Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Sleeper Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Distal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short 2Nd Toe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short 2Nd Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Qt Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Rib-Polydactyly Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Rib-Polydactyly Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short-Rib Thoracic Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short-Rib Thoracic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Hard Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Hard Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spondyloperipheral Dysplasia Short Ulna Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spondyloperipheral Dysplasia Short Ulna in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Bowel Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Bowel Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short 5Th Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Rib Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Rib Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Middle Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Chordae Tendineae Of The Mitral Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Chordae Tendineae Of The Mitral Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Chordae Tendineae Of The Tricuspid Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Chordae Tendineae Of The Tricuspid Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Bowel Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Bowel in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short 3Rd Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Digit Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Digit in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Fifth Metatarsal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Fifth Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Diaphyses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Poor Short-Term Memory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Poor Short-Term Memory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short 5Th Toe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short 5Th Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Relatively Short Spine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Relatively Short Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Nose Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Distal Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Neck Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Lower Third Of Face Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Lower Third Of Face in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Thorax Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Thorax in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Columella Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Columella in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Neck (In Some Patients) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Neck (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Upturned Nose Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Upturned Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short 1St Metacarpal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 1St Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Toe Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Extremities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Extremities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Phalanx Of Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Philtrum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Philtrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Long Bone Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Metacarpals With Rounded Proximal Ends Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Metacarpals With Rounded Proximal Ends in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Palm Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Palm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Memory, Short-Term Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Memory, Short-Term in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Stepped Shuffling Gait Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Stepped Shuffling Gait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Humerus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Humerus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Ribs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Ribs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Tibia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Tibia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Leg Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Leg in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Palpebral Fissure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Palpebral Fissure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Upper Lip Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Sternum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Sternum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Nasal Septum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Nasal Septum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Telomere Length Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Telomere Length in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Clavicle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Clavicle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Femoral Neck Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Femoral Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Iliac Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Iliac Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Metacarpal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Frenulum Of Tongue Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Frenulum Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Metatarsal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short 2Nd Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short 2Nd Metacarpal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 2Nd Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short 5Th Metacarpal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 5Th Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Middle Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Proximal Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Ear Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Sperm Flagella Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Sperm Flagella in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Tubular Bones Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Tubular Bones Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short 4Th Metacarpal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 4Th Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Fourth Metatarsal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Fourth Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Sacroiliac Notch Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Sacroiliac Notch in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short 3Rd Metacarpal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 3Rd Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Face Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Face in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Deficit In Phonologic Short-Term Memory Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deficit In Phonologic Short-Term Memory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Third Metatarsal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Third Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short First Metatarsal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short First Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short-Rib Thoracic Dysplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short-Rib Thoracic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Mandibular Rami Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Mandibular Rami in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Cord Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Nasal Bridge Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Nasal Bridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dorsolateral Bowed, Short Radii Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dorsolateral Bowed, Short Radii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Forearm Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Forearm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Uvula Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Uvula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short 4Th Toe Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 4Th Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Dental Roots Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Dental Roots in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Fetal Femur Length Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Fetal Femur Length in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Bowed Radii Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Bowed Radii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
regulation of short-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset.
short-term memory Gene Set From GO Biological Process Annotations 2023 genes participating in the short-term memory biological process from the curated GO Biological Process Annotations 2023 dataset.
short-term synaptic potentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
short-chain fatty acid catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
short-chain fatty acid transport Gene Set From GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2023 dataset.
short-chain fatty acid metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of short-term synaptic potentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
short-chain fatty acid transmembrane transport Gene Set From GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset.
short-chain fatty acid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of short-term synaptic potentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
short-chain fatty acid transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the short-chain fatty acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
short-chain-acyl-CoA dehydrogenase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the short-chain-acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
short-chain carboxylesterase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the short-chain carboxylesterase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
short tibia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short tibia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short humerus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short humerus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short radius Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short radius phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short ulna Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short ulna phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short mandible Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short mandible phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short maxilla Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short maxilla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short zygomatic bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short zygomatic bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short ribs Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short ribs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short femur Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short femur phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short rostral-caudal axis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short metacarpal bones Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short metacarpal bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short metatarsal bones Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short metatarsal bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short vertebral body Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short vertebral body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short tail Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short tail phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short premaxilla Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short premaxilla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short Meckel's cartilage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short Meckel's cartilage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short lower incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short lower incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short upper incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short nasal septum Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short nasal septum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short vertebral column Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short vertebral column phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short snout Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short snout phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short limbs Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short limbs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short fibula Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short fibula phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short oviduct Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short oviduct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short photoreceptor outer segment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short photoreceptor outer segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short vibrissae Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short vibrissae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short sternum Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short sternum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short photoreceptor inner segment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short malleus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short malleus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short stride length Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short stride length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short frontal bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short frontal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short hair Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short ears Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short ears phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short nasal bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short nasal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short scapula Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short scapula phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short lumbar vertebrae Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short lumbar vertebrae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short face Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short face phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short basicranium Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short basicranium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short trachea Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short trachea phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short endolymphatic duct Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short endolymphatic duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short cochlear outer hair cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short estrous cycle Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short estrous cycle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short diestrus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short diestrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short estrus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short estrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal incus short process morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal incus short process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short inner hair cell stereocilia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short sperm flagellum Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short sperm flagellum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short nails Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short nails phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short excitatory postsynaptic current decay time Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short excitatory postsynaptic current decay time phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short outer hair cell stereocilia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short zygomatic arch Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short facial bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short facial bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short scala media Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short scala media phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short soft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short soft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short ureter Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short ureter phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short proestrus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short proestrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short styloid process Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short styloid process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short cochlear hair cell stereocilia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short tongue Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short tongue phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short neck Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short neck phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short perineum Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short perineum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent incus short process Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent incus short process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal short-term spatial reference memory Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal short-term spatial reference memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short philtrum Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short philtrum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short malleus manubrium Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short malleus manubrium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short umbilical cord Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short umbilical cord phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short Tomes' process Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short Tomes' process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short gestation period Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short gestation period phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short uterine horn Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short uterine horn phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short femur neck Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short femur neck phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short chin Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short chin phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal short-term object recognition memory Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal short-term object recognition memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short ilium Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short ilium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short temporal bone squamous part Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short temporal bone squamous part phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short tooth root Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short tooth root phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short nasal bridge Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short nasal bridge phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short vestibular hair cell stereocilia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short vestibular hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short metestrus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short metestrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short forehead Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short forehead phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short presphenoid bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short presphenoid bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short kidney papilla Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short kidney papilla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short mandibular coronoid process Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short mandibular coronoid process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short excitatory postsynaptic current rise time Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short excitatory postsynaptic current rise time phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short parietal bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short parietal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short tibia Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the short tibia phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Human - Tonsil - L2 - Short lived IgM+ PC Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - Short lived IgM+ PC cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Short-lived effector cell (SLEC)_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Short-lived effector cell (SLEC)_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Mitochondrial short-chain enoyl-CoA hydratase deficiency 1 Gene Set From Reactome Pathways 2024 proteins participating in the Mitochondrial short-chain enoyl-CoA hydratase deficiency 1 pathway from the Reactome Pathways 2024 dataset.
regulation of short-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2025 dataset.
short-term memory Gene Set From GO Biological Process Annotations 2025 genes participating in the short-term memory biological process from the curated GO Biological Process Annotations 2025 dataset.
short-term synaptic potentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
short-chain fatty acid catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the short-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
short-chain fatty acid transport Gene Set From GO Biological Process Annotations 2025 genes participating in the short-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2025 dataset.
short-chain fatty acid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the short-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of short-term synaptic potentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
short-chain fatty acid transmembrane transport Gene Set From GO Biological Process Annotations 2025 genes participating in the short-chain fatty acid transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset.
short-chain fatty acid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the short-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of short-term synaptic potentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
short-chain fatty acyl-CoA dehydrogenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the short-chain fatty acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
short-chain fatty acid transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the short-chain fatty acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
short-chain 2-methyl fatty acyl-CoA dehydrogenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the short-chain 2-methyl fatty acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
short-chain carboxylesterase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the short-chain carboxylesterase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
short-chain fatty acyl-CoA hydrolase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the short-chain fatty acyl-CoA hydrolase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
short-chain fatty acid-CoA ligase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the short-chain fatty acid-CoA ligase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease short-rib thoracic dysplasia 9 with or without polydactyly from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Short QT syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Short QT syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
SHORT syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease SHORT syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Short chain acyl-CoA dehydrogenase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Short chain acyl-CoA dehydrogenase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Short bowel syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short bowel syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short QT syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short QT syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
SHORT syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease SHORT syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 9 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 6 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 6 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short chain acyl-CoA dehydrogenase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short chain acyl-CoA dehydrogenase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 10 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 14 with polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 14 with polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 8 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 8 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 11 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 13 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 13 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 7 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 7 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-chain collagen trimer Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the short-chain collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
short-chain collagen trimer Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the short-chain collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Short QT syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short-rib thoracic dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short-rib thoracic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short fetal femur length Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short fetal femur length phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital short bowel syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital short bowel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SHORT syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SHORT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short rib-polydactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short rib-polydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short ribs Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short ribs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short rib polydactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short rib polydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short telomere length Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short telomere length phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short 5th finger Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short 5th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
LDL cholesterol levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Short-term memory (visuospatial task) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Short-term memory (visuospatial task) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Short-term memory (digit-span task) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Short-term memory (digit-span task) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep duration (short sleep) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (short sleep) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypertension risk in short sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Baseline cortisol levels in response to low dose short synacthen test in corticosteroid treated asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Baseline cortisol levels in response to low dose short synacthen test in corticosteroid treated asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Peak cortisol response to low dose short synacthen test in corticosteroid treated asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peak cortisol response to low dose short synacthen test in corticosteroid treated asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fasting glucose change (short-term) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fasting glucose change (short-term) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

neonatal short-limb short stature Gene Set

Neonatal Short-Limb Short Stature Gene Set

neonatal short-trunk short stature Gene Set

Neonatal Short-Trunk Short Stature Gene Set

childhood-onset short-trunk short stature Gene Set

disproportionate short-trunk short stature Gene Set

lethal short-limbed short stature Gene Set

Lethal Short-Limbed Short Stature Gene Set

Childhood-Onset Short-Trunk Short Stature Gene Set

Disproportionate Short-Trunk Short Stature Gene Set

Infancy Onset Short-Trunk Short Stature Gene Set

Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome Gene Set

encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice Gene Set

jaundice, neonatal; neonatal jaundice Gene Set

glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice Gene Set

Short stature, idiopathic, autosomal Gene Set

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

Ectodermal dysplasia/short stature syndrome Gene Set

Short stature, idiopathic, X-linked Gene Set

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

Microcephaly, short stature, and impaired glucose metabolism Gene Set

Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set

Yakut short stature syndrome Gene Set

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

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

Mental Retardation, X-Linked, with Short Stature Gene Set

Short Stature, Idiopathic, Autosomal Gene Set

Short Stature, Idiopathic, X-Linked Gene Set

short stature Gene Set

idiopathic short stature Gene Set

moderately short stature Gene Set

short stature Gene Set

mesomelic short stature Gene Set

disproportionate short stature Gene Set

mild short stature Gene Set

proportionate short stature Gene Set

severe short stature Gene Set

short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

ectodermal dysplasia/short stature syndrome Gene Set

short stature Gene Set

short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

mental retardation, x-linked, with short stature Gene Set

microcephaly, short stature, and impaired glucose metabolism Gene Set

osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene Set

short stature with microcephaly and distinctive facies Gene Set

short stature, idiopathic familial Gene Set

short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

Ear, Patella, Short Stature Syndrome Gene Set

Short Stature Gene Set

Short Stature Homeobox Deficiency Gene Set

Pituitary Short Stature Gene Set

Short Stature, Idiopathic, Autosomal Gene Set

Joint Laxity, Short Stature, And Myopia Gene Set

Facial Dysmorphism, Immunodeficiency, Livedo, And Short Stature Gene Set

Shox-Related Short Stature Gene Set

Short Stature Gene Set

Short Stature, Ctcae Gene Set

Disproportionate Short Stature Gene Set

Proportionate Short Stature Gene Set

Mild Short Stature Gene Set

Moderately Short Stature Gene Set

Short Stature, Postnatal Gene Set

Mesomelic Short Stature Gene Set

Intellectual developmental disorder with short stature and behavioral abnormalities Gene Set

Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies Gene Set

Short stature, hearing loss, retinitis pigmentosa, and distinctive facies Gene Set

Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature Gene Set

X-linked intellectual disability-short stature-overweight syndrome Gene Set

SHOX-related short stature Gene Set

Short stature Gene Set

Short stature due to growth hormone secretagogue receptor deficiency Gene Set

Short stature due to partial GHR deficiency Gene Set

SHOX-related short stature Gene Set