Congenital Cerebellar Ataxia

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Results for "Congenital Cerebellar Ataxia": 1001 gene sets

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Congenital Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-progressive congenital cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-progressive congenital cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cognitive impairment with or without cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, deafness, and narcolepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia, cerebellar ataxia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia cerebellar ataxia mental deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aniridia cerebellar ataxia mental deficiency from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Cayman Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Cayman Type from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar ataxia; Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar ataxia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonprogressive cerebellar ataxia Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cerebellar ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cerebellar Ataxia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebellar Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
cognitive impairment with or without cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, cerebellar, cayman type Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, cerebellar, cayman type phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, nonprogressive, with mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, nonprogressive, with mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, deafness, and narcolepsy, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, deafness, and narcolepsy, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
Autosomal Dominant Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessie Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessie Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Marie Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Marie Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cognitive Impairment With Or Without Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cognitive Impairment With Or Without Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spectrin-Associated Autosomal Recessive Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spectrin-Associated Autosomal Recessive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Cerebellar Ataxia Type 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Cerebellar Ataxia Type 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nonprogressive Cerebellar Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonprogressive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Gait Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Gait Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autosomal dominant cerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant cerebellar ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebellar ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive cerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive cerebellar ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nonprogressive cerebellar ataxia with mental retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nonprogressive cerebellar ataxia with mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia, mental retardation and dysequlibrium syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia, mental retardation and dysequlibrium syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant cerebellar ataxia, deafness and narcolepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cerebellar ataxia, deafness and narcolepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cayman type cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cayman type cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 47 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Abortive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abortive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ITPR1-associated cerebellar ataxia spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ITPR1-associated cerebellar ataxia spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar ataxia-hypogonadism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-hypogonadism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
spinocerebellar ataxia 29, congenital nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 29, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
Congenital Non-Progressive Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Non-Progressive Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Heart Defects, Congenital, And Other Congenital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
cerebellar hemisphere Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
dorsolateral (non-cerebellar) part of isA Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in dorsolateral (non-cerebellar) part of isA relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
mantle zone of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in mantle zone of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar white matter Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar white matter relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
white matter of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in white matter of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
lateral (dentate) cerebellar nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral (dentate) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar nuclei of CbH Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar nuclei of CbH relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cerebellar nuclei Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cerebellar nuclei relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cortex of cerebellar hemisphere Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cortex of cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
intermediate (interpositus) cerebellar nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in intermediate (interpositus) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cortex of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cortex of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
superficial stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
medial (fastigial) cerebellar nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in medial (fastigial) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar nuclei of CbV Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar nuclei of CbV relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
superficial stratum of cerebellar hemisphere Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
intermediate stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in intermediate stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cerebellar cortex Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cerebellar cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
periventricular stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in periventricular stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar cortex_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_26 pcw_F_12949 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_11 yrs_F_12289 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_8 yrs_M_12981 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_4 mos_M_12890 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_19 yrs_F_12832 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_37 pcw_M_263195015 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_35 pcw_F_12295 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_35 pcw_F_12295 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar vermis Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar vermis relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
cerebellar mossy fiber Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cerebellar mossy fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cerebellar mossy fiber Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cerebellar mossy fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 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.
CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 from the curated CTD Gene-Disease Associations dataset.
Cerebellar Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Diseases from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.
cerebellar disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cerebellar disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cerebellar disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar liponeurocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar liponeurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar angioblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar angioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myoclonic cerebellar dyssynergia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myoclonic cerebellar dyssynergia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
primary cerebellar degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary cerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
huntington disease; myoclonic cerebellar dyssynergia; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease huntington disease; myoclonic cerebellar dyssynergia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive Gene Set From GAD Gene-Disease Associations genes associated with the disease brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar medulloblastomas and cutaneous basal cell carcinomas. Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar medulloblastomas and cutaneous basal cell carcinomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar neoplasms; medulloblastoma Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar neoplasms; medulloblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar volume Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar volume in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cerebellar in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
CSTB_KO_GSE47516_18_mouse_brain (P7 cerebellum, P30 cerebellum, cerebellar granule cells) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the CSTB_KO_GSE47516_18_mouse_brain (P7 cerebellum, P30 cerebellum, cerebellar granule cells) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
regulation of cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar cortex structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar cortex structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell layer morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell layer morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar cortex formation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar cortex formation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar cortex morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar cortex morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granule cell precursor tangential migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granule cell precursor tangential migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar molecular layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar molecular layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell layer structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell layer structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar cortex development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar cortex development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
radial glia guided migration of cerebellar granule cell Gene Set From GO Biological Process Annotations 2015 genes participating in the radial glia guided migration of cerebellar granule cell biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
smoothened signaling pathway involved in regulation of cerebellar granule cell precursor cell proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the smoothened signaling pathway involved in regulation of cerebellar granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell layer maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell layer maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granule cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granule cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar mossy fiber Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cerebellar mossy fiber cellular component from the curated GO Cellular Component Annotations 2015 dataset.
abnormality of the cerebellar peduncle Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the inferior half of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the inferior half of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thickened superior cerebellar peduncle Gene Set From HPO Gene-Disease Associations genes associated with the thickened superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
agenesis of cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the agenesis of cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar cyst Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar cyst phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
elongated superior cerebellar peduncle Gene Set From HPO Gene-Disease Associations genes associated with the elongated superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dysgenesis of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the dysgenesis of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hemisphere hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hemisphere hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
disorganization of the anterior cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the disorganization of the anterior cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the superior cerebellar peduncle Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar malformation Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar calcifications Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hemangioblastoma Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hemangioblastoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
loss of purkinje cells in the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the loss of purkinje cells in the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dense calcifications in the cerebellar dentate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the dense calcifications in the cerebellar dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cerebellar Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebellar Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebellar Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebellar Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myoclonic Cerebellar Dyssynergia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myoclonic Cerebellar Dyssynergia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebellar degeneration-related protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cerebellar degeneration-related protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
thin cerebellar molecular layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar molecular layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar lobule formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar lobule formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar hemisphere morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar hemisphere morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar purkinje cell layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar purkinje cell layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebellar granule cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebellar granule cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellar foliation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellar granule cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellar granule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin cerebellar granule layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar granule layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar granule layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar golgi cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar golgi cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar peduncle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar peduncle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
reduced cerebellar foliation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the reduced cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellar lobules Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellar lobules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar granule cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar granule cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar cortex morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delaminated cerebellar granule layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delaminated cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ectopic cerebellar granule cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ectopic cerebellar granule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar plate morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar granule cell migration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar granule cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar foliation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellar granule layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar granule cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar granule cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
hemangioblastoma, cerebellar, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the hemangioblastoma, cerebellar, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral-cerebellar-coloboma syndrome, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral-cerebellar-coloboma syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile cerebellar-retinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
pancreatic and cerebellar agenesis Gene Set From OMIM Gene-Disease Associations genes associated with the pancreatic and cerebellar agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term cerebellar in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
cerebellar granule cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebellar granule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebellar nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebellar nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebellar cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebellar cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebellar purkinje cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebellar purkinje cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Function Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Function in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Lesion Nos Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Lesion Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Liponeurocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Liponeurocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Ischaemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Ischaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy, Cerebellar Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cortical Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Decompression Injury Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Decompression Injury in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thickened Superior Cerebellar Peduncle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thickened Superior Cerebellar Peduncle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysgenesis Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysgenesis Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Granule Cell Hypertrophy And Megalencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Granule Cell Hypertrophy And Megalencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cognitive Affective Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cognitive Affective Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Degeneration, Subacute Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Degeneration, Subacute in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Cerebellar Degeneration, Anti-Yo-Associated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Cerebellar Degeneration, Anti-Yo-Associated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic Cerebellar Dyssynergia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic Cerebellar Dyssynergia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Absence Of Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Absence Of Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Cortical Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Cortical Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymicrogyria, Perisylvian, With Cerebellar Hypoplasia And Arthrogryposis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymicrogyria, Perisylvian, With Cerebellar Hypoplasia And Arthrogryposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Agenesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Agenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Degenerations, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Degenerations, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Hemisphere Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Hemisphere Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Cerebellar Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cerebellar Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Cerebral, Cerebellar, Coloboma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Cerebral, Cerebellar, Coloboma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Cerebellar Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebellar Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Signs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Dysmetria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Dysmetria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Vermis Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Elongated Superior Cerebellar Peduncle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elongated Superior Cerebellar Peduncle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Loss Of Purkinje Cells In The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Purkinje Cells In The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Purkinje Layer Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Purkinje Layer Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Vermis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Cyst Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Cyst in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Dysplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Calcifications Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Calcifications in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fusion Of The Cerebellar Hemispheres Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fusion Of The Cerebellar Hemispheres in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Superior Cerebellar Peduncle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Superior Cerebellar Peduncle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Disorganization Of The Anterior Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disorganization Of The Anterior Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dense Calcifications In The Cerebellar Dentate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dense Calcifications In The Cerebellar Dentate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Gliosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Gliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Morphology Of The Cerebellar Cortex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Morphology Of The Cerebellar Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Hypoplasia With Endosteal Sclerosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Hypoplasia With Endosteal Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Hemiataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Hemiataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Cerebellar Peduncle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Cerebellar Peduncle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Small Cerebellar Cortex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Cerebellar Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Inferior Half Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Inferior Half Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cerebellar granule cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar granule cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar Purkinje cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar Purkinje cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar Purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar Purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar granule cell precursor tangential migration Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar granule cell precursor tangential migration biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar granular layer maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar granular layer maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
radial glia guided migration of cerebellar granule cell Gene Set From GO Biological Process Annotations 2023 genes participating in the radial glia guided migration of cerebellar granule cell biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar cortex maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar cortex maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar mossy fiber Gene Set From GO Cellular Component Annotations 2023 proteins localized to the cerebellar mossy fiber cellular component from the curated GO Cellular Component Annotations 2023 dataset.
abnormal cerebellar granule cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar granule cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar plate morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar plate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar molecular layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin cerebellar molecular layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin cerebellar molecular layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar foliation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar granule layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar granule layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebellar granule cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebellar granule cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar Purkinje cell layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar Purkinje cell layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin cerebellar granule layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin cerebellar granule layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellar granule cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellar granule cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delaminated cerebellar granule layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delaminated cerebellar granule layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cerebellar foliation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar cortex morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellar foliation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar lobule formation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar lobule formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellar lobules Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellar lobules phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
reduced cerebellar foliation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ectopic cerebellar granule cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic cerebellar granule cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar granule cell migration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar granule cell migration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar Golgi cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar Golgi cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellar granule layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellar granule layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebellar granule cell precursor proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebellar granule cell precursor proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar glomerulus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar glomerulus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar peduncle morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar peduncle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar granule cell precursor proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar granule cell precursor proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar hemisphere morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar hemisphere morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cerebellar granule cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cerebellar granule cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Brain - Cerebellar Hemisphere Gene Set From GTEx Tissue Gene Expression Profiles 2023 genes with high or low expression in Brain - Cerebellar Hemisphere relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.
Cerebellar interneuron_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Cerebellar interneuron_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
cerebellar granule cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar granule cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar Purkinje cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar Purkinje cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar Purkinje cell-granule cell precursor cell signaling Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar Purkinje cell-granule cell precursor cell signaling biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar granule cell precursor tangential migration Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar granule cell precursor tangential migration biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar granular layer maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar granular layer maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
radial glia guided migration of cerebellar granule cell Gene Set From GO Biological Process Annotations 2025 genes participating in the radial glia guided migration of cerebellar granule cell biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar cortex maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar cortex maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar mossy fiber Gene Set From GO Cellular Component Annotations 2025 proteins localized to the cerebellar mossy fiber cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Cerebellar disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebellar disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebellar medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary cerebellar degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary cerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myoclonic cerebellar dyssynergia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myoclonic cerebellar dyssynergia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile cerebellar-retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar liponeurocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar liponeurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar vermis medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar vermis medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lissencephaly 7 with cerebellar hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lissencephaly 7 with cerebellar hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar angioblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar angioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebellar cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebellar Purkinje cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebellar Purkinje cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebellar granule cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebellar granule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebellar nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebellar nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebellar mossy fiber Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cerebellar mossy fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Cerebellar granule cell to Purkinje cell synapse Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cerebellar granule cell to Purkinje cell synapse cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Cerebellar climbing fiber to Purkinje cell synapse Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cerebellar climbing fiber to Purkinje cell synapse cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Cerebellar mossy fiber Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cerebellar mossy fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Infantile cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability-cerebellar hypoplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability-cerebellar hypoplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebellar-retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar-facial-dental syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar-facial-dental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hemangioblastoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hemangioblastoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar vermis hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar vermis hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked cerebral-cerebellar-coloboma syndrome syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked cerebral-cerebellar-coloboma syndrome 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.
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.
Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dysgenesis of the cerebellar vermis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dysgenesis of the cerebellar vermis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal cerebellar vermis morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal cerebellar vermis morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-telangiectasia-like disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia autosomal recessive 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia autosomal recessive 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic ataxia, type 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia, spastic, 4, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia, spastic, 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia with vitamin E deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia with vitamin E deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia, sensory, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia, sensory, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic ataxia 5, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic ataxia 5, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Friedreich's ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Friedreich's ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic ataxia Charlevoix-Saguenay type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic ataxia Charlevoix-Saguenay type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrokeratodermia with ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrokeratodermia with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, X-linked 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive myoclonus epilepsy with ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive myoclonus epilepsy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia autosomal recessive with axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia autosomal recessive with axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia-like disorder 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia-like disorder 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-oculomotor apraxia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-oculomotor apraxia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 40 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 40 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 35 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 35 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adult onset ataxia with oculomotor apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult onset ataxia with oculomotor apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia, spastic, 2, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia, spastic, 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia autosomal recessive 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia autosomal recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic ataxia type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic ataxia type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 27 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 26 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 29 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia 38 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia 38 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar Ataxia 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia 15 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia 12 from the curated CTD Gene-Disease Associations dataset.
Ataxia Telangiectasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia Telangiectasia from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia 17 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia 17 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia 10 from the curated CTD Gene-Disease Associations dataset.
Gait Ataxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gait Ataxia from the curated CTD Gene-Disease Associations dataset.
Ataxia, Spastic, 3, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia, Spastic, 3, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Anemia, sideroblastic spinocerebellar ataxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, sideroblastic spinocerebellar ataxia from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia 11 from the curated CTD Gene-Disease Associations dataset.
Posterior column ataxia with retinitis pigmentosa Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Posterior column ataxia with retinitis pigmentosa from the curated CTD Gene-Disease Associations dataset.
Episodic ataxia with nystagmus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic ataxia with nystagmus from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 26 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 26 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 28 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 28 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia, Autosomal Recessive 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia, Autosomal Recessive 9 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia, Autosomal Recessive 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia, Autosomal Recessive 8 from the curated CTD Gene-Disease Associations dataset.
SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy from the curated CTD Gene-Disease Associations dataset.
Ataxia with vitamin E deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia with vitamin E deficiency from the curated CTD Gene-Disease Associations dataset.
ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia, X-Linked 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia, X-Linked 5 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 8 from the curated CTD Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.
Spastic ataxia Charlevoix-Saguenay type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic ataxia Charlevoix-Saguenay type from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, autosomal recessive 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 3 from the curated CTD Gene-Disease Associations dataset.
Sensorimotor neuropathy with ataxia, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensorimotor neuropathy with ataxia, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Friedreich Ataxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Friedreich Ataxia from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 3 from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 1 from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 7 from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 5 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, autosomal recessive 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 4 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, autosomal recessive 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 1 from the curated CTD Gene-Disease Associations dataset.
Ataxia, Spastic, 1, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia, Spastic, 1, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, X-linked, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 4 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, X-linked, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 3 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, X-linked, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 2 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, autosomal recessive 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 6 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, autosomal recessive 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 5 from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 6 from the curated CTD Gene-Disease Associations dataset.
Friedreich Ataxia 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Friedreich Ataxia 1 from the curated CTD Gene-Disease Associations dataset.
Friedreich Ataxia 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Friedreich Ataxia 2 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia, Autosomal Recessive 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 13 from the curated CTD Gene-Disease Associations dataset.
Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset.
Fragile X Tremor Ataxia Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fragile X Tremor Ataxia Syndrome from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 20 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 20 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia 29 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia 29 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 23 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 23 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 21 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 21 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 27 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 27 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 25 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 25 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 14 from the curated CTD Gene-Disease Associations dataset.
Ataxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar Ataxia 31 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar Ataxia 31 from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia 30 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia 30 from the curated CTD Gene-Disease Associations dataset.
infantile onset spinocerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease infantile onset spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
episodic ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease episodic ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ataxia telangiectasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ataxia telangiectasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
x-linked sideroblastic anemia with ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease x-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
spinocerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
friedreich ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease friedreich ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
infantile onset spinocerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease infantile onset spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
friedreich ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease friedreich ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sideroblastic anemia with spinocerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sideroblastic anemia with spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ataxia telangiectasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ataxia telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
x-linked sideroblastic anemia with ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease x-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinocerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
episodic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease episodic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ataxia with oculomotor apraxia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ataxia with oculomotor apraxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ataxia with oculomotor apraxia type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ataxia with oculomotor apraxia type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set From GAD Gene-Disease Associations genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomegaly; friedreich ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomegaly; friedreich ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia type 6 Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia type 6 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x associated tremor/ataxia syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x associated tremor/ataxia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia-telangiectasia Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia-telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
friedreich ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease friedreich ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia; fragile x syndrome; tremor Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; fragile x syndrome; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathies; friedreich ataxia; scoliosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathies; friedreich ataxia; scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
episodic ataxia type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease episodic ataxia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
huntington's disease; ataxia (sca) Gene Set From GAD Gene-Disease Associations genes associated with the disease huntington's disease; ataxia (sca) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x-associated tremor/ataxia syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x-associated tremor/ataxia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia; fragile x syndrome; huntington disease; tremor Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia; fragile x syndrome; huntington disease; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia (sca) Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia (sca) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosomal instability; friedreich ataxia; Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosomal instability; friedreich ataxia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia; fragile x syndrome; fragile x syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia; fragile x syndrome; fragile x syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gait ataxia; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease gait ataxia; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
friedreichs ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease friedreichs ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term ataxia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
spastic ataxia Gene Set From HPO Gene-Disease Associations genes associated with the spastic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
gait ataxia Gene Set From HPO Gene-Disease Associations genes associated with the gait ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb ataxia Gene Set From HPO Gene-Disease Associations genes associated with the limb ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic ataxia Gene Set From HPO Gene-Disease Associations genes associated with the episodic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ataxia Gene Set From HPO Gene-Disease Associations genes associated with the ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive gait ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive gait ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensory ataxia Gene Set From HPO Gene-Disease Associations genes associated with the sensory ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive truncal ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive truncal ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
truncal ataxia Gene Set From HPO Gene-Disease Associations genes associated with the truncal ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Gait Ataxia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Gait Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ataxia Telangiectasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ataxia Telangiectasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Friedreich Ataxia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Friedreich Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ataxia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
ataxia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ataxia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
?spinocerebellar ataxia, autosomal recessive 15 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia, autosomal recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia, autosomal recessive 17 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia, autosomal recessive 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia with isolated vitamin e deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia with isolated vitamin e deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 7 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 6 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 5 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 3, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 3, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia 34 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia 34 phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia 30 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia 30 phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, sideroblastic, with ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, sideroblastic, with ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 6 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 7 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 8 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 7 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 8 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 18 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 19 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 17 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 14 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 15 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 12 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 13 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 10 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 11 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia-telangiectasia-like disorder Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 35 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 35 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 36 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 36 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 31 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 31 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 32 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 32 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 38 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 38 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocrebellar ataxia, autosomal recessive 12 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocrebellar ataxia, autosomal recessive 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy with ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia-telangiectasia Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-telangiectasia phenotype from the curated OMIM Gene-Disease Associations dataset.
?ataxia-telangiectasia-like disorder Gene Set From OMIM Gene-Disease Associations genes associated with the ?ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From OMIM Gene-Disease Associations genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
friedreich ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the friedreich ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 16 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 14 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 13 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 11 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 10 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, x-linked 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, x-linked 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
fragile x tremor/ataxia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the fragile x tremor/ataxia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, posterior column, with retinitis pigmentosa Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, posterior column, with retinitis pigmentosa phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
friedreich ataxia with retained reflexes Gene Set From OMIM Gene-Disease Associations genes associated with the friedreich ataxia with retained reflexes phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia-ocular apraxia-2 Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-ocular apraxia-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia 40 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia 40 phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia 26 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia 26 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia-oculomotor apraxia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-oculomotor apraxia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
mitochondrial recessive ataxia syndrome (includes sando and scae) Gene Set From OMIM Gene-Disease Associations genes associated with the mitochondrial recessive ataxia syndrome (includes sando and scae) phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia, x-linked 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, sensory, 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, sensory, 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 23 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 21 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 20 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 27 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 25 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 28 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 28 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia/myokymia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia/myokymia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
friedreich ataxia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the friedreich ataxia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, spastic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, spastic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, spastic, 5, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, spastic, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive with axonal neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive with axonal neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia, charlevoix-saguenay type Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia, charlevoix-saguenay type phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term ataxia in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
ataxia-telangiectasic cancer Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease ataxia-telangiectasic cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
spinocerebellar ataxia type 14 Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease spinocerebellar ataxia type 14 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
ataxia-telangiectasia Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease ataxia-telangiectasia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
spinocerebellar ataxia type 1 Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease spinocerebellar ataxia type 1 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Friedreich Ataxia 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Friedreich Ataxia 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ataxia With Central Nervous System Hypomyelinization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ataxia With Central Nervous System Hypomyelinization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinocerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinocerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Friedreich Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Friedreich Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fragile X Tremor/Ataxia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fragile X Tremor/Ataxia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Opsoclonus-Myoclonus Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Opsoclonus-Myoclonus Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Onset Spinocerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Onset Spinocerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erythrokeratodermia With Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erythrokeratodermia With Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Column Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Column Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Column Ataxia With Retinitis Pigmentosa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Column Ataxia With Retinitis Pigmentosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Harding Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Harding Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prickle1-Related Progressive Myoclonus Epilepsy With Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prickle1-Related Progressive Myoclonus Epilepsy With Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gait Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gait Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Gait Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Gait Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sporadic Adult-Onset Ataxia Of Unknown Etiology Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sporadic Adult-Onset Ataxia Of Unknown Etiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gait Ataxia, Sensory Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gait Ataxia, Sensory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Truncal Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Truncal Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intermittent Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
ataxia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ataxia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
PKC gamma calcium signaling in ataxia Gene Set From WikiPathways Pathways 2024 proteins participating in the PKC gamma calcium signaling in ataxia pathway from the WikiPathways Pathways 2024 dataset.
Defective SLC1A3 causes episodic ataxia 6 (EA6) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC1A3 causes episodic ataxia 6 (EA6) pathway from the Reactome Pathways 2024 dataset.
Hereditary ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia with axonal neuropathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Charlevoix-Saguenay spastic ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Episodic ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Episodic ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked sideroblastic anemia with ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 6 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia type 6 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Friedreich ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Friedreich ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia type 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ataxia telangiectasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ataxia telangiectasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 36 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia type 36 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 8 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive spinocerebellar ataxia 8 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fragile X-associated tremor/ataxia syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fragile X-associated tremor/ataxia syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked hereditary ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked hereditary ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fragile X-associated tremor/ataxia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fragile X-associated tremor/ataxia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked hereditary ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked hereditary ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ataxia telangiectasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ataxia telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Friedreich ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Friedreich ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
hypotonia, ataxia, and delayed development syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypotonia, ataxia, and delayed development syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked sideroblastic anemia with ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 34 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 34 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia 45 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Friedreich ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Friedreich ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ataxia-telangiectasia-like disorder-2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ataxia-telangiectasia-like disorder-2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 19/22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 19/22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease stress-induced childhood-onset neurodegeneration with variable ataxia and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ataxia with oculomotor apraxia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ataxia with oculomotor apraxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Friedreich ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Friedreich ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ataxia-telangiectasia-like disorder-1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ataxia-telangiectasia-like disorder-1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charlevoix-Saguenay spastic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant sensory ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant sensory ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with eye movement abnormalities and ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with eye movement abnormalities and ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ataxia with oculomotor apraxia type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ataxia with oculomotor apraxia type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ataxia-oculomotor apraxia type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ataxia-oculomotor apraxia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 33 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 33 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Gait ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gait ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia - telangiectasia variant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - telangiectasia variant phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-telangiectasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive ataxia due to ubiquinone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive ataxia due to ubiquinone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Friedreich ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Friedreich ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile onset spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile onset spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia - oculomotor apraxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - oculomotor apraxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charlevoix-Saguenay spastic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-hypogonadism-choroidal dystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-hypogonadism-choroidal dystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-telangiectasia-like disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia and retinitis pigmentosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia and retinitis pigmentosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Posterior column ataxia-retinitis pigmentosa syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Posterior column ataxia-retinitis pigmentosa syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary episodic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary episodic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant sensory ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant sensory ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinocerebellar ataxia / Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinocerebellar ataxia / phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic and progressive ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chronic and progressive ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia _ Neurologic Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia _ Neurologic phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fragile X-associated tremor/ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fragile X-associated tremor/ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sideroblastic Anemia and Ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sideroblastic Anemia and Ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recessive mitochondrial ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recessive mitochondrial ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spasticity-ataxia-gait anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spasticity-ataxia-gait anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive spastic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive spastic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia Neuropathy Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia Neuropathy Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cayman ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cayman ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-pancytopenia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-pancytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PUM1-associated developmental disability-ataxia-seizure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PUM1-associated developmental disability-ataxia-seizure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia telangiectasi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia telangiectasi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive gait ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive gait ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
NUS1-related epilepsy-myoclonus-ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the NUS1-related epilepsy-myoclonus-ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinocerebellar ataxia Gene Set From KEGG Pathways 2026 proteins participating in the Spinocerebellar ataxia pathway from the KEGG Pathways 2026 dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hyperplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hyperplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital human immunodeficiency virus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital human immunodeficiency virus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige 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.
Diarrhea 5, with tufting enteropathy, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diarrhea 5, with tufting enteropathy, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vertical talus, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vertical talus, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital generalized lipodystrophy type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IV, congenital neuromuscular Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial paresis, hereditary congenital, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital glucose-galactose malabsorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital glucose-galactose malabsorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with cores Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aphakia, congenital primary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aphakia, congenital primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, congenital generalized, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital contractural arachnodactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital contractural arachnodactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital absence of salivary gland Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nystagmus 6, congenital, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nystagmus 6, congenital, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Afibrinogenemia, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Afibrinogenemia, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital amegakaryocytic thrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital amegakaryocytic thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, fast-channel Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal recessive congenital 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diarrhea 3, secretory sodium, congenital, syndromic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diarrhea 3, secretory sodium, congenital, syndromic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 3, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hypoplasia, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital secretory diarrhea, chloride type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Testicular anomalies with or without congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL 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.
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart disease, multiple types, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, slow-channel congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Indifference to pain, congenital, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Indifference to pain, congenital, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contractural syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart defects, multiple types, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital erythropoietic porphyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital erythropoietic porphyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
congenital neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with excess of thin myofilaments Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett syndrome, congenital variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2k Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, with excess of muscle spindles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital lactase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal recessive form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal recessive form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 6, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1Q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1v Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adult i Blood Group with or without Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, compton-north Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital cystic disease of liver Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type Ix Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital order of glycosylation type 1r Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital order of glycosylation type 1r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital central hypoventilation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital ocular coloboma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital ocular coloboma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

Congenital Cerebellar Ataxia Gene Set

Non-progressive congenital cerebellar ataxia Gene Set

Cognitive impairment with or without cerebellar ataxia Gene Set

Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

Cerebellar ataxia, deafness, and narcolepsy Gene Set

Aniridia, cerebellar ataxia, and mental retardation Gene Set

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

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

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

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

Aniridia cerebellar ataxia mental deficiency Gene Set

Cerebellar Ataxia, Cayman Type Gene Set

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

Cerebellar Ataxia Gene Set

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

cerebellar ataxia Gene Set

cerebellar ataxia; Gene Set

cerebellar ataxia Gene Set

nonprogressive cerebellar ataxia Gene Set

progressive cerebellar ataxia Gene Set

Cerebellar Ataxia Gene Set

cognitive impairment with or without cerebellar ataxia Gene Set

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

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

ataxia, cerebellar, cayman type Gene Set

migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set

cerebellar ataxia, nonprogressive, with mental retardation Gene Set

cerebellar ataxia Gene Set

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

cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

cerebellar ataxia, deafness, and narcolepsy, autosomal dominant Gene Set

Autosomal Dominant Cerebellar Ataxia Gene Set

Progressive Cerebellar Ataxia Gene Set

Autosomal Recessie Cerebellar Ataxia Gene Set

Cerebellar Ataxia Gene Set

Marie Cerebellar Ataxia Gene Set

Acute Cerebellar Ataxia Gene Set

Cognitive Impairment With Or Without Cerebellar Ataxia Gene Set

Spectrin-Associated Autosomal Recessive Cerebellar Ataxia Gene Set

Autosomal Recessive Cerebellar Ataxia Type 1 Gene Set

Cerebellar Ataxia Gene Set

Nonprogressive Cerebellar Ataxia Gene Set

Cerebellar Gait Ataxia Gene Set

Autosomal dominant cerebellar ataxia Gene Set

Cerebellar ataxia Gene Set

Autosomal recessive cerebellar ataxia Gene Set

Autosomal dominant cerebellar ataxia Gene Set

Cerebellar ataxia Gene Set

Autosomal recessive cerebellar ataxia Gene Set

Cerebellar ataxia type 48 Gene Set

Cerebellar ataxia type 41 Gene Set

Cerebellar ataxia type 42 Gene Set

Nonprogressive cerebellar ataxia with mental retardation Gene Set

Cerebellar ataxia, mental retardation and dysequlibrium syndrome Gene Set

Autosomal dominant cerebellar ataxia, deafness and narcolepsy Gene Set

Cayman type cerebellar ataxia Gene Set

Cerebellar ataxia type 47 Gene Set

Cerebellar ataxia type 43 Gene Set

X-linked cerebellar ataxia Gene Set

Cerebellar ataxia type 9 Gene Set

Abortive cerebellar ataxia Gene Set

Cerebellar ataxia Gene Set

Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Gene Set

Autosomal dominant cerebellar ataxia Gene Set

X-linked progressive cerebellar ataxia Gene Set

Autosomal recessive cerebellar ataxia Gene Set

Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome Gene Set

Progressive cerebellar ataxia Gene Set

Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome Gene Set

ITPR1-associated cerebellar ataxia spectrum disorder Gene Set

Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome Gene Set

Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set

Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome Gene Set

Cerebellar ataxia-hypogonadism syndrome Gene Set

Hereditary cerebellar ataxia Gene Set

Congenital cerebellar hypoplasia Gene Set

Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set