Progressive cerebellar ataxia

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Results for "Progressive cerebellar ataxia": 1003 gene sets

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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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, 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Epilepsy, progressive myoclonic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaze palsy, familial horizontal, with progressive scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy, progressive, with ovarian failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy, progressive, with ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive pseudorheumatoid dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperpigmentation, familial progressive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure 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.
Progressive intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 2b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis with progressive nerve deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis with progressive nerve deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive myositis ossificans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive myositis ossificans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic Epilepsies, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myoclonic Epilepsies, Progressive from the curated CTD Gene-Disease Associations dataset.
Cataract, Nuclear Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Nuclear Progressive from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset.
Gliosis, Familial Progressive Subcortical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.
Osseous Heteroplasia, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osseous Heteroplasia, Progressive from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive, 2 from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive, 3 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Progressive Myoclonic, 1b Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Progressive Myoclonic, 1b from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.
Chorioretinal atrophy, progressive bifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset.
Macrothrombocytopenia progressive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrothrombocytopenia progressive deafness from the curated CTD Gene-Disease Associations dataset.
Erythrokeratodermia, Progressive Symmetric Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrokeratodermia, Progressive Symmetric from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset.
Progressive hearing loss stapes fixation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive hearing loss stapes fixation from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.
Arthropathy, progressive pseudorheumatoid, of childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthropathy, progressive pseudorheumatoid, of childhood from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy, Progressive Multifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy, Progressive Multifocal from the curated CTD Gene-Disease Associations dataset.
Progressive Familial Heart Block, Type Ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.
Bulbar Palsy, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bulbar Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.
Ophthalmoplegia, Chronic Progressive External Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, Chronic Progressive External from the curated CTD Gene-Disease Associations dataset.
Nephropathy, Progressive, with Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy, Progressive, with Deafness from the curated CTD Gene-Disease Associations dataset.
Progressive supranuclear palsy atypical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive supranuclear palsy atypical from the curated CTD Gene-Disease Associations dataset.
Renal Failure, Progressive, with Hypertension Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Failure, Progressive, with Hypertension from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Supranuclear Palsy, Progressive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
chronic progressive external ophthalmoplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive myoclonus epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease progressive myoclonus epilepsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive supranuclear palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease progressive supranuclear palsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive supranuclear palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive supranuclear palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive bulbar palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive bulbar palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic progressive external ophthalmoplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic progressive external ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive multifocal leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive multifocal leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
rapidly progressive glomerulonephritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rapidly progressive glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive myoclonus epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive myoclonus epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
slowly progressive als Gene Set From GAD Gene-Disease Associations genes associated with the disease slowly progressive als in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial atypical progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia, primary progressive; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ophthalmoplegia, chronic progressive external Gene Set From GAD Gene-Disease Associations genes associated with the disease ophthalmoplegia, chronic progressive external in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
primary progressive aphasia Gene Set From GAD Gene-Disease Associations genes associated with the disease primary progressive aphasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neurodegenerative diseases; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dominant progressive deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant progressive deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia, primary progressive; heredodegenerative disorders, nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; heredodegenerative disorders, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rapidly progressive familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain diseases; neurodegenerative diseases; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease brain diseases; neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive av-block and anomalous venous return Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive av-block and anomalous venous return in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive external ophthalmoplegia Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive external ophthalmoplegia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; huntington disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive renal damage Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive renal damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; huntington disease; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; huntington disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term progressive in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
progressive supranuclear palsy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease progressive supranuclear palsy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
progressive cataract Gene Set From HPO Gene-Disease Associations genes associated with the progressive cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive inability to walk Gene Set From HPO Gene-Disease Associations genes associated with the progressive inability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive congenital scoliosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive congenital scoliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive visual field defects Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symmetrical progressive peripheral demyelination Gene Set From HPO Gene-Disease Associations genes associated with the symmetrical progressive peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spastic paraplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic paraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cone degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive cone degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive vitiligo Gene Set From HPO Gene-Disease Associations genes associated with the progressive vitiligo phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive neurologic deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive neurologic deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spastic quadriplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic quadriplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive psychomotor deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive psychomotor deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive reticulate hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the progressive reticulate hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive fusion 2nd-5th pip joints Gene Set From HPO Gene-Disease Associations genes associated with the progressive fusion 2nd-5th pip joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive extrapyramidal movement disorder Gene Set From HPO Gene-Disease Associations genes associated with the progressive extrapyramidal movement disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive inspiratory stridor Gene Set From HPO Gene-Disease Associations genes associated with the progressive inspiratory stridor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive choreoathetosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive choreoathetosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spasticity Gene Set From HPO Gene-Disease Associations genes associated with the progressive spasticity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive peripheral neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive sclerosis of skull base Gene Set From HPO Gene-Disease Associations genes associated with the progressive sclerosis of skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive clavicular acroosteolysis Gene Set From HPO Gene-Disease Associations genes associated with the progressive clavicular acroosteolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive alopecia Gene Set From HPO Gene-Disease Associations genes associated with the progressive alopecia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subacute progressive viral hepatitis Gene Set From HPO Gene-Disease Associations genes associated with the subacute progressive viral hepatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intellectual disability, progressive Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability, progressive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive central visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive language deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive language deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the progressive hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hypotrichosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive hypotrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive pulmonary function impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive pulmonary function impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive forgetfulness Gene Set From HPO Gene-Disease Associations genes associated with the progressive forgetfulness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive microcephaly Gene Set From HPO Gene-Disease Associations genes associated with the progressive microcephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive alveolar ridge hypertropy Gene Set From HPO Gene-Disease Associations genes associated with the progressive alveolar ridge hypertropy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive proximal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive macrocephaly Gene Set From HPO Gene-Disease Associations genes associated with the progressive macrocephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive external ophthalmoplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive night blindness Gene Set From HPO Gene-Disease Associations genes associated with the progressive night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive macular scarring Gene Set From HPO Gene-Disease Associations genes associated with the progressive macular scarring phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive ptosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive ptosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive calcification of costochondral cartilage Gene Set From HPO Gene-Disease Associations genes associated with the progressive calcification of costochondral cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cervical vertebral spine fusion Gene Set From HPO Gene-Disease Associations genes associated with the progressive cervical vertebral spine fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive conductive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive conductive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rapidly progressive Gene Set From HPO Gene-Disease Associations genes associated with the rapidly progressive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive leukoencephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive flexion contractures Gene Set From HPO Gene-Disease Associations genes associated with the progressive flexion contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive disorder Gene Set From HPO Gene-Disease Associations genes associated with the progressive disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive ophthalmoplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Chronic Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myoclonic Epilepsies, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myoclonic Epilepsies, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Bulbar Palsy, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bulbar Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Supranuclear Palsy, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Supranuclear Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aphasia, Primary Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aphasia, Primary Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ophthalmoplegia, Chronic Progressive External Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ophthalmoplegia, Chronic Progressive External phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Progressive rod-cone degeneration protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Progressive rod-cone degeneration protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Progressive ankylosis Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Progressive ankylosis protein domain from the InterPro Predicted Protein Domain Annotations dataset.
progressive muscle weakness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
progressive hair loss Gene Set From MPO Gene-Phenotype Associations gene mutations causing the progressive hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
deafness, x-linked 1, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, x-linked 1, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive canalicular Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive canalicular phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 2b (lafora) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 2b (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal dominant, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive familial heart block, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
macrothrombocytopenia and progressive sensorineural deafness Gene Set From OMIM Gene-Disease Associations genes associated with the macrothrombocytopenia and progressive sensorineural deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive atypical Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive atypical phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperpigmentation, familial progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aphasia, primary progressive Gene Set From OMIM Gene-Disease Associations genes associated with the aphasia, primary progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepiphyseal dysplasia tarda with progressive arthropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepiphyseal dysplasia tarda with progressive arthropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy, progressive x-linked, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy, progressive, with ovarian failure Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, progressive, with ovarian failure phenotype from the curated OMIM Gene-Disease Associations dataset.
osseous heteroplasia, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the osseous heteroplasia, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.
nephropathy, progressive, with deafness Gene Set From OMIM Gene-Disease Associations genes associated with the nephropathy, progressive, with deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
gaze palsy, horizontal, with progressive scoliosis Gene Set From OMIM Gene-Disease Associations genes associated with the gaze palsy, horizontal, with progressive scoliosis phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
arthropathy, progressive pseudorheumatoid, of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the arthropathy, progressive pseudorheumatoid, of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions 3 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, progressive, with or without lipodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 27, nuclear progressive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 27, nuclear progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
heart block, progressive, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the heart block, progressive, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 1a (unverricht and lundborg) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 1a (unverricht and lundborg) phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 1b Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 2a (lafora) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 2a (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set From Reactome Pathways 2014 proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways dataset.
Primary Progressive Aphasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Progressive Aphasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy (Without Rod Involvement) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cgvhd Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cgvhd in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Intrahepatic Cholestasis (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Intrahepatic Cholestasis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Slowly Progressive Insulin Dependent Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slowly Progressive Insulin Dependent Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Supranuclear Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Supranuclear Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Pseudorheumatoid Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Pseudorheumatoid Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Primary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Primary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Progressive External Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Progressive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Intellectual Disability And Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Intellectual Disability And Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Progressive Nonfluent Aphasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Progressive Nonfluent Aphasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Distal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Post Hemorrhagic Ventricular Dilatation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Post Hemorrhagic Ventricular Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Dementia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Progressive Chorea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Progressive Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Bulbar Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Secondary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Secondary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Periodontitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Ptosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Ptosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Brain Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Brain Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cardiomyopathic Lentiginosis Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cardiomyopathic Lentiginosis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Non-Small Cell Lung Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Non-Small Cell Lung Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ophthalmoplegia, Progressive Supranuclear Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ophthalmoplegia, Progressive Supranuclear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supranuclear Palsy, Progressive, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Atrophy, Progressive Bifocal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy, Progressive Bifocal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Failure, Progressive, With Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Failure, Progressive, With Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pf-Ild-Progressive Fibrosing Interstitial Lung Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pf-Ild-Progressive Fibrosing Interstitial Lung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Logopenic Progressive Aphasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Logopenic Progressive Aphasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalomyelitis With Rigidity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalomyelitis With Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symmetrical Progressive Peripheral Demyelination Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symmetrical Progressive Peripheral Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Hearing Loss Stapes Fixation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Hearing Loss Stapes Fixation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Chorea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Piebaldism, Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Piebaldism, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Hyper And Hypopigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Hyper And Hypopigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Reticulate Hyperpigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Reticulate Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Subcortical Gliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Subcortical Gliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 1, Atypical Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supranuclear Palsy, Progressive, 1, Atypical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Impairment And Progressive Phthisis Bulbi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Impairment And Progressive Phthisis Bulbi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macrothrombocytopenia And Progressive Sensorineural Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macrothrombocytopenia And Progressive Sensorineural Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cavitating Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cavitating Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysphagia, Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysphagia, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Congenital Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Congenital Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Polyneuropathy With Bilateral Striatal Necrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Polyneuropathy With Bilateral Striatal Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Progressive Bulbar Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Proximal Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Myoclonic Epilepsy With Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Myoclonic Epilepsy With Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Familial Heart Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Familial Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Leukoencephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Peripheral Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Night Blindness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Night Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Neoplastic Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Neoplastic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Neurologic Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Neurologic Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spasticity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Proximal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Microcephaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intellectual Disability, Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intellectual Disability, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Quadriplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Cervical Vertebral Spine Fusion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Cervical Vertebral Spine Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraparesis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Flexion Contractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Flexion Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Macrocephaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Macrocephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Inability To Walk Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Inability To Walk in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Pes Cavus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Pes Cavus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subacute Progressive Viral Hepatitis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subacute Progressive Viral Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Rapidly Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rapidly Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Psychomotor Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Psychomotor Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Paraparesis, Chronic Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paraparesis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Extrapyramidal Movement Disorder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Extrapyramidal Movement Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Intervertebral Space Narrowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Intervertebral Space Narrowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Clavicular Acroosteolysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Clavicular Acroosteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Conductive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Conductive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Field Defects Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Field Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Distal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sensorineural Hearing Loss, Progressive Bilateral Postlingual Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sensorineural Hearing Loss, Progressive Bilateral Postlingual in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Ventriculomegaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Language Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Language Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Calcification Of Costochondral Cartilage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Calcification Of Costochondral Cartilage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Alveolar Ridge Hypertropy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Alveolar Ridge Hypertropy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Forgetfulness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Forgetfulness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hyperpigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Choreoathetosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Choreoathetosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Loss Of Facial Adipose Tissue Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Loss Of Facial Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Extrapyramidal Muscular Rigidity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Extrapyramidal Muscular Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Leg Bowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Leg Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Vitiligo Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Vitiligo in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hypotrichosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hypotrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Pulmonary Function Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Pulmonary Function Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Fusion 2Nd-5Th Pip Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Fusion 2Nd-5Th Pip Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Sclerosis Of Skull Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Sclerosis Of Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Inspiratory Stridor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Inspiratory Stridor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Alopecia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
progressive muscle weakness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased sperm progressive motility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased sperm progressive motility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
progressive hair loss Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sperm progressive motility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm progressive motility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set From Reactome Pathways 2024 proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways 2024 dataset.
Chronic progressive external ophthalmoplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive familial heart block Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive familial heart block from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive bulbar palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive bulbar palsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive familial intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive supranuclear palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive supranuclear palsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 1B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with progressive myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive osseous heteroplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive osseous heteroplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive pseudorheumatoid arthropathy of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive bulbar palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive bulbar palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive supranuclear palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive supranuclear palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic progressive external ophthalmoplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic progressive external ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary progressive aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary progressive aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic tetraplegia, thin corpus callosum, and progressive microcephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic tetraplegia, thin corpus callosum, and progressive microcephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive non-fluent aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive non-fluent aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive leukoencephalopathy with ovarian failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive leukoencephalopathy with ovarian failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive multifocal leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive multifocal leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rapidly progressive glomerulonephritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rapidly progressive glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive relapsing multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive relapsing multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Logopenic progressive aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Logopenic progressive aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type IA Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type IA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive osseous heteroplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive osseous heteroplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type IB Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type IB in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial progressive hyperpigmentation with or without hypopigmentation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial progressive hyperpigmentation with or without hypopigmentation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset progressive encephalopathy with brain atrophy and thin corpus callosum Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset progressive encephalopathy with brain atrophy and thin corpus callosum in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive pseudorheumatoid arthropathy of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic progressive polyneuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic progressive polyneuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual impairment and progressive phthisis bulbi in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive distal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive proximal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive pseudorheumatoid dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive familial intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive cone dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive cone dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive familial heart block Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive familial heart block phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear palsy-parkinsonism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive supranuclear palsy-parkinsonism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive supranuclear ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive osseous heteroplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive osseous heteroplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive scapulohumeroperoneal distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive myositis ossificans Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive myositis ossificans phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy-progressive myoclonic epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-progressive spastic diplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-progressive spastic diplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary progressive aphasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary progressive aphasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Skeletal dysplasia and progressive central nervous system degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal dysplasia and progressive central nervous system degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive demyelinating neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive demyelinating neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive neurologic deterioration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive neurologic deterioration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive bulbar palsy of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive bulbar palsy of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary progressive multiple sclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary progressive multiple sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive spasticity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive spasticity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive childhood encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive childhood encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive retinal dystrophy due to retinol transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment and progressive phthisis bulbi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-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.
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.

Harmonizome 3.0

progressive cerebellar ataxia Gene Set

Progressive Cerebellar Ataxia Gene Set

Progressive cerebellar ataxia Gene Set

Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set

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

X-linked progressive cerebellar ataxia Gene Set

Non-progressive congenital cerebellar ataxia Gene Set

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

Progressive Cerebellar Degeneration Gene Set

Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene Set

frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set

basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set

chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene Set

Cognitive impairment with or without cerebellar ataxia 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

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

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

Congenital Cerebellar Ataxia Gene Set

Autosomal Dominant 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

Autosomal recessive cerebellar ataxia Gene Set

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

Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome Gene Set

ITPR1-associated cerebellar ataxia spectrum disorder Gene Set