ataxia, spastic, 4

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Results for "ataxia, spastic, 4": 840 gene sets

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ataxia, spastic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, spastic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
paraparesis, tropical spastic; tropical spastic paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease paraparesis, tropical spastic; tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Ataxia, spastic, 4, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia, spastic, 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic ataxia 5, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic ataxia 5, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic 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.
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.
Ataxia, Spastic, 3, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia, Spastic, 3, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Spastic 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.
Ataxia, Spastic, 1, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia, Spastic, 1, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
spastic ataxia Gene Set From HPO Gene-Disease Associations genes associated with the spastic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic ataxia 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 3, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 3, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, spastic, 5, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, spastic, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia, charlevoix-saguenay type Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia, charlevoix-saguenay type phenotype from the curated OMIM Gene-Disease Associations dataset.
Spastic Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Charlevoix-Saguenay spastic ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spastic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charlevoix-Saguenay spastic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic ataxia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charlevoix-Saguenay spastic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charlevoix-Saguenay spastic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive spastic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive spastic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 46, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 46, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 48, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 48, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 4, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 54, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 54, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 5A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 5A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 11, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 11, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 57, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 57, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 72, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 72, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 35 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 35 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 44, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 44, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 72, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 72, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 26 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 55, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 55, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 63, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 63, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 31, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 31, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 39 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 56, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 56, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 30, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 30, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 33, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 33, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 45, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 45, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 42, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 42, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 24 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 24 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 20, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 20, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 32, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 32, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 36, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 36, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 34, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 34, X-Linked from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia type 5A, recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia type 5A, recessive from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 7, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 7, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Hereditary spastic paralysis, infantile onset ascending Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 4, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 4, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia type 5B, recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia type 5B, recessive from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 31, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 31, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 16, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 16, X-linked from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 42, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 42, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 33, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 33, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 17 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 17 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 11, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 11, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 10, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 10, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 44, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 44, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 2, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 2, X-linked from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 25, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 25, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Paraparesis, Spastic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Paraparesis, Spastic from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 15, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 15, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 2 from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 39, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 39, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 9, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 9, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 37, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 37, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia-50, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia-50, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 3, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 3, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 38, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 38, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 23 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 23 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 14, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 14, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 29, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 29, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 6, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 6, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 8, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 8, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Hereditary from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 27, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 27, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 1 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 13, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 13, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 19, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 19, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 18, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 18, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
hereditary spastic paraplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary spastic paraplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
spastic quadriplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic quadriplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic hemiplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic hemiplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic entropion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic entropion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic diplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic diplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary spastic paraplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary spastic paraplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic ectropion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic ectropion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tropical spastic paraparesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tropical spastic paraparesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
motor neuron disease; paraparesis, spastic Gene Set From GAD Gene-Disease Associations genes associated with the disease motor neuron disease; paraparesis, spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spastic paraplegia Gene Set From GAD Gene-Disease Associations genes associated with the disease spastic paraplegia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spastic paralysis Gene Set From GAD Gene-Disease Associations genes associated with the disease spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary spastic paraparesis due to a frame shift mutat Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-1 associated myelopathy/tropical spastic; paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-1 associated myelopathy/tropical spastic; paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary spastic angina. Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary spastic angina. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary spastic angina Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary spastic angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelopathy/tropical spastic paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease myelopathy/tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spastic paraplegia, hereditary Gene Set From GAD Gene-Disease Associations genes associated with the disease spastic paraplegia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile-onset ascending hereditary spastic paralysis Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; spastic paraplegia, hereditary Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; spastic paraplegia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-i infections; paraparesis, tropical spastic Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i infections; paraparesis, tropical spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spastic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term spastic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
spastic dysarthria Gene Set From HPO Gene-Disease Associations genes associated with the spastic dysarthria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
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 spastic quadriplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic quadriplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic tetraplegia Gene Set From HPO Gene-Disease Associations genes associated with the spastic tetraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic tetraparesis Gene Set From HPO Gene-Disease Associations genes associated with the spastic tetraparesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic diplegia Gene Set From HPO Gene-Disease Associations genes associated with the spastic diplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic gait Gene Set From HPO Gene-Disease Associations genes associated with the spastic gait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic paraparesis Gene Set From HPO Gene-Disease Associations genes associated with the spastic paraparesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spastic paraplegia Gene Set From HPO Gene-Disease Associations genes associated with the spastic paraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Paraparesis, Tropical Spastic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paraparesis, Tropical Spastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Paraparesis, Spastic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paraparesis, Spastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spastic Paraplegia, Hereditary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spastic Paraplegia, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
spastic paraplegia 8, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 8, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 13, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 13, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 5a, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 5a, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 12, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 12, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 72, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 72, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 29, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 29, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 16, x-linked, complicated Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 16, x-linked, complicated phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 18, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 18, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, with spastic paraplegia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, with spastic paraplegia phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 32, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 32, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 53, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 53, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 19, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 19, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 33, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 33, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 64 Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 64 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 30, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 30, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 42, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 42, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 43, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 43, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 45, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 45, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 25, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 25, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 39, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 39, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 55, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 55, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 24, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 24, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 28, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 28, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 37, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 11, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 11, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 2, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 46, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 46, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 38, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 38, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 26, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 26, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 51, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 51, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 47, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 47, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 27, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 27, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 9, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 9, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 34, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 34, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 52, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 52, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 14, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 14, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 56, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 56, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia, optic atrophy, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 35, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 35, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 10, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 10, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 41, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 41, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral palsy, spastic quadriplegic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral palsy, spastic quadriplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
alzheimer disease, type 3, with spastic paraparesis and unusual plaques Gene Set From OMIM Gene-Disease Associations genes associated with the alzheimer disease, type 3, with spastic paraparesis and unusual plaques phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 50, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 50, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 44, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 44, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 63 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 63 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 15, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 15, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 36, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 36, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 72, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 72, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 49, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 49, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 7, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 7, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 3a, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 3a, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 54, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 54, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, spastic quadriplegia, and mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
silver spastic paraplegia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the silver spastic paraplegia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 61, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 61, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 48, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 48, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 57, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 57, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral palsy, spastic quadriplegic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral palsy, spastic quadriplegic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 45 Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 45 phenotype from the curated OMIM Gene-Disease Associations dataset.
alzheimer disease, type 3, with spastic paraparesis and apraxia Gene Set From OMIM Gene-Disease Associations genes associated with the alzheimer disease, type 3, with spastic paraparesis and apraxia phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 31, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 31, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paralysis, infantile onset ascending Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset.
Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) pathway from the Reactome Pathways dataset.
Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Functional Diarrhoea (Due To Spastic Colon) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Functional Diarrhoea (Due To Spastic Colon) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Tetraparesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Tetraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tropical Spastic Paraparesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tropical Spastic Paraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Quadriplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Palsy, Spastic Quadriplegic, 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Hereditary Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complicated Hereditary Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complicated Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Autosomal Dominant Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Autosomal Dominant Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Spastic Paralysis, Infantile Onset Ascending Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Spastic Paralysis, Infantile Onset Ascending in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Pure Hereditary Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pure Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Diplegia Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Diplegia Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mt-Atp6-Related Mitochondrial Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mt-Atp6-Related Mitochondrial Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary X-Linked Recessive Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary X-Linked Recessive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked, Spastic Paraplegia, Hereditary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked, Spastic Paraplegia, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraparesis, Spastic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paraparesis, Spastic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spastic Gait Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spastic Gait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic 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 Spastic Paraparesis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Coronary Spastic Angina Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Coronary Spastic Angina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spastic/Hyperactive Bladder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spastic/Hyperactive Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spastic Paraparetic Gait Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spastic Paraparetic Gait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spastic Paraplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC33A1 causes spastic paraplegia 42 (SPG42) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC33A1 causes spastic paraplegia 42 (SPG42) pathway from the Reactome Pathways 2024 dataset.
Hereditary spastic paraplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 31 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 31 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 15 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 15 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 35 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 35 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 7 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 7 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 3A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 3A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 5A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 5A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 8 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 8 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 11 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 11 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 49 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 49 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 17 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 17 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary spastic paraplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic quadriplegic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic quadriplegic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic 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.
Hereditary spastic paraplegia 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tropical spastic paraparesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tropical spastic paraparesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 61 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 61 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 73 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 73 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 39 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 39 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic diplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic diplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 76 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 76 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 49 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 49 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 81 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 81 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 78 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 78 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic hemiplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic hemiplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 75 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 75 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 9A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 9A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 63 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 63 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 45 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 77 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 77 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 70 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 70 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 5A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 5A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 64 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 64 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 47 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 3A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 84 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 84 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 57 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 57 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic entropion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic entropion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 51 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic monoplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic monoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 72A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 72A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 87 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 87 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 9B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 9B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 82 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 82 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic quadriplegic cerebral palsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic quadriplegic cerebral palsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia 85 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 85 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraparesis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraparesis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic tetraplegia and axial hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic tetraplegia and axial hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
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.
SPG11-related spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SPG11-related spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic gait Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic gait phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic diplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic diplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive complex spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive complex spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraplegia-severe developmental delay-epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia-severe developmental delay-epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SPAST-related spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SPAST-related spastic paraplegia 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.
Spastic hemiparesis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic hemiparesis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pure or complex autosomal recessive spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pure or complex autosomal recessive spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inherited spastic paresis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited spastic paresis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraplegia 30b Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia 30b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraplegia 18a Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia 18a phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ATL1-related spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ATL1-related spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic cerebral palsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic cerebral palsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-telangiectasia-like disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cognitive impairment with or without cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
spinocerebellar ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x associated tremor/ataxia syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x associated tremor/ataxia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia-telangiectasia Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia-telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
friedreich ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease friedreich ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia; fragile x syndrome; tremor Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; fragile x syndrome; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathies; friedreich ataxia; scoliosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathies; friedreich ataxia; scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
episodic ataxia type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease episodic ataxia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
huntington's disease; ataxia (sca) Gene Set From GAD Gene-Disease Associations genes associated with the disease huntington's disease; ataxia (sca) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x-associated tremor/ataxia syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x-associated tremor/ataxia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia; fragile x syndrome; huntington disease; tremor Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia; fragile x syndrome; huntington disease; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia (sca) Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia (sca) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosomal instability; friedreich ataxia; Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosomal instability; friedreich ataxia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia; fragile x syndrome; fragile x syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia; fragile x syndrome; fragile x syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gait ataxia; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease gait ataxia; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
friedreichs ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease friedreichs ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term ataxia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
gait ataxia Gene Set From HPO Gene-Disease Associations genes associated with the gait ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb ataxia Gene Set From HPO Gene-Disease Associations genes associated with the limb ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic ataxia Gene Set From HPO Gene-Disease Associations genes associated with the episodic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ataxia Gene Set From HPO Gene-Disease Associations genes associated with the ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive gait ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive gait ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensory ataxia Gene Set From HPO Gene-Disease Associations genes associated with the sensory ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive cerebellar ataxia Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive truncal ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive truncal ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
truncal ataxia Gene Set From HPO Gene-Disease Associations genes associated with the truncal ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
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.
Gait Ataxia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Gait Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ataxia Telangiectasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ataxia Telangiectasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Friedreich Ataxia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Friedreich Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
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.
Ataxia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
ataxia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ataxia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
?spinocerebellar ataxia, autosomal recessive 15 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia, autosomal recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia, autosomal recessive 17 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia, autosomal recessive 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia with isolated vitamin e deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia with isolated vitamin e deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 7 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 6 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 5 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
?spinocerebellar ataxia 34 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia 34 phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia 30 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia 30 phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, sideroblastic, with ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, sideroblastic, with ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 6 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 7 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 8 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 7 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 8 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 18 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 19 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 17 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 14 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 15 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 12 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 13 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 10 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 11 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia-telangiectasia-like disorder Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 35 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 35 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 36 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 36 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 31 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 31 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 32 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 32 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 38 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 38 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocrebellar ataxia, autosomal recessive 12 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocrebellar ataxia, autosomal recessive 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
?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.
leukoencephalopathy with ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
ataxia-telangiectasia Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-telangiectasia phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
?ataxia-telangiectasia-like disorder Gene Set From OMIM Gene-Disease Associations genes associated with the ?ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From OMIM Gene-Disease Associations genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
friedreich ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the friedreich ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 16 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 14 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 13 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 11 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 10 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, x-linked 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, x-linked 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
fragile x tremor/ataxia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the fragile x tremor/ataxia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, posterior column, with retinitis pigmentosa Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, posterior column, with retinitis pigmentosa phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
friedreich ataxia with retained reflexes Gene Set From OMIM Gene-Disease Associations genes associated with the friedreich ataxia with retained reflexes phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
ataxia-ocular apraxia-2 Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-ocular apraxia-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
?spinocerebellar ataxia 40 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia 40 phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia 26 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia 26 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia-oculomotor apraxia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-oculomotor apraxia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
mitochondrial recessive ataxia syndrome (includes sando and scae) Gene Set From OMIM Gene-Disease Associations genes associated with the mitochondrial recessive ataxia syndrome (includes sando and scae) phenotype from the curated OMIM Gene-Disease Associations dataset.
?spinocerebellar ataxia, x-linked 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?spinocerebellar ataxia, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, sensory, 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, sensory, 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 23 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 21 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 20 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 27 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 25 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 28 Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 28 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia/myokymia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia/myokymia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
friedreich ataxia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the friedreich ataxia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia 29, congenital nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia 29, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
spinocerebellar ataxia, autosomal recessive with axonal neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive with axonal neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
ataxia Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term ataxia in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
ataxia-telangiectasic cancer Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease ataxia-telangiectasic cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
spinocerebellar ataxia type 14 Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease spinocerebellar ataxia type 14 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
ataxia-telangiectasia Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease ataxia-telangiectasia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
spinocerebellar ataxia type 1 Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease spinocerebellar ataxia type 1 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Friedreich Ataxia 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Friedreich Ataxia 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ataxia With Central Nervous System Hypomyelinization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ataxia With Central Nervous System Hypomyelinization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinocerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinocerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Friedreich Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Friedreich Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fragile X Tremor/Ataxia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fragile X Tremor/Ataxia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Episodic Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Paraneoplastic Opsoclonus-Myoclonus Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Opsoclonus-Myoclonus Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Onset Spinocerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Onset Spinocerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erythrokeratodermia With Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erythrokeratodermia With Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Column Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Column Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Column Ataxia With Retinitis Pigmentosa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Column Ataxia With Retinitis Pigmentosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Harding Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Harding Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
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.
Gait Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gait Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Gait Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Gait Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sporadic Adult-Onset Ataxia Of Unknown Etiology Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sporadic Adult-Onset Ataxia Of Unknown Etiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
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.
Gait Ataxia, Sensory Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gait Ataxia, Sensory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Truncal Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Truncal Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intermittent Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
ataxia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ataxia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
PKC gamma calcium signaling in ataxia Gene Set From WikiPathways Pathways 2024 proteins participating in the PKC gamma calcium signaling in ataxia pathway from the WikiPathways Pathways 2024 dataset.
Defective SLC1A3 causes episodic ataxia 6 (EA6) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC1A3 causes episodic ataxia 6 (EA6) pathway from the Reactome Pathways 2024 dataset.
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.
Hereditary ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
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.
Spinocerebellar ataxia with axonal neuropathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia with axonal neuropathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
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.
Episodic ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Episodic ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked sideroblastic anemia with ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 6 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia type 6 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Friedreich ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Friedreich ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia type 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ataxia telangiectasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ataxia telangiectasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 36 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia type 36 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 8 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive spinocerebellar ataxia 8 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fragile X-associated tremor/ataxia syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fragile X-associated tremor/ataxia syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked hereditary ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked hereditary ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Hereditary ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fragile X-associated tremor/ataxia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fragile X-associated tremor/ataxia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked hereditary ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked hereditary ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Ataxia telangiectasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ataxia telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Friedreich ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Friedreich ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Spinocerebellar ataxia with axonal neuropathy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
hypotonia, ataxia, and delayed development syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypotonia, ataxia, and delayed development syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Spinocerebellar ataxia type 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked sideroblastic anemia with ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 34 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 34 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia 45 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Friedreich ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Friedreich ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Spinocerebellar ataxia type 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Spinocerebellar ataxia type 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
ataxia-telangiectasia-like disorder-2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ataxia-telangiectasia-like disorder-2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 19/22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 19/22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease stress-induced childhood-onset neurodegeneration with variable ataxia and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Spinocerebellar ataxia type 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Spinocerebellar ataxia type 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ataxia with oculomotor apraxia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ataxia with oculomotor apraxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked 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.
X-linked spinocerebellar ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Friedreich ataxia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Friedreich ataxia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
ataxia-telangiectasia-like disorder-1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ataxia-telangiectasia-like disorder-1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant sensory ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant sensory ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with eye movement abnormalities and ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with eye movement abnormalities and ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ataxia with oculomotor apraxia type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ataxia with oculomotor apraxia type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinocerebellar ataxia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinocerebellar ataxia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ataxia-oculomotor apraxia type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ataxia-oculomotor apraxia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive spinocerebellar ataxia 33 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive spinocerebellar ataxia 33 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Gait ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gait ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia - telangiectasia variant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - telangiectasia variant phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-telangiectasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive ataxia due to ubiquinone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive ataxia due to ubiquinone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Friedreich ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Friedreich ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile onset spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile onset spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia - oculomotor apraxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - oculomotor apraxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
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.
Ataxia-hypogonadism-choroidal dystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-hypogonadism-choroidal dystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-telangiectasia-like disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia and retinitis pigmentosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia and retinitis pigmentosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
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.
Posterior column ataxia-retinitis pigmentosa syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Posterior column ataxia-retinitis pigmentosa syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary episodic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary episodic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant 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 dominant sensory ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant sensory ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinocerebellar ataxia / Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinocerebellar ataxia / phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic and progressive ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chronic and progressive ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia _ Neurologic Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia _ Neurologic phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
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.
Fragile X-associated tremor/ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fragile X-associated tremor/ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sideroblastic Anemia and Ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sideroblastic Anemia and Ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recessive mitochondrial ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recessive mitochondrial ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
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.
Spasticity-ataxia-gait anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spasticity-ataxia-gait anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
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.
Ataxia Neuropathy Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia Neuropathy Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cayman ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cayman ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia-pancytopenia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia-pancytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
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.
PUM1-associated developmental disability-ataxia-seizure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PUM1-associated developmental disability-ataxia-seizure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia telangiectasi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia telangiectasi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
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.
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.
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.
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
NUS1-related epilepsy-myoclonus-ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the NUS1-related epilepsy-myoclonus-ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinocerebellar ataxia Gene Set From KEGG Pathways 2026 proteins participating in the Spinocerebellar ataxia pathway from the KEGG Pathways 2026 dataset.

Harmonizome 3.0

ataxia, spastic, 4 Gene Set

paraparesis, tropical spastic; tropical spastic paraparesis Gene Set

htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis Gene Set

Ataxia, spastic, 4, autosomal recessive Gene Set

Spastic ataxia 5, autosomal recessive Gene Set

Spastic ataxia Charlevoix-Saguenay type Gene Set

Ataxia, spastic, 2, autosomal recessive Gene Set

Ataxia, Spastic, 3, Autosomal Recessive Gene Set

SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE Gene Set

Spastic ataxia Charlevoix-Saguenay type Gene Set

Ataxia, Spastic, 1, Autosomal Dominant Gene Set

spastic ataxia Gene Set

spastic ataxia 2, autosomal recessive Gene Set

spastic ataxia 3, autosomal recessive Gene Set

spastic ataxia 1, autosomal dominant Gene Set

ataxia, spastic, 5, autosomal recessive Gene Set

spastic ataxia, charlevoix-saguenay type Gene Set

Spastic Ataxia Gene Set

Charlevoix-Saguenay spastic ataxia Gene Set

Spastic ataxia Gene Set

Spastic ataxia 1 Gene Set

Spastic ataxia 5 Gene Set

Spastic ataxia 4 Gene Set

Spastic ataxia 8 Gene Set

Charlevoix-Saguenay spastic ataxia Gene Set

Spastic ataxia 2 Gene Set

Spastic ataxia 3 Gene Set

Spastic ataxia Gene Set

Charlevoix-Saguenay spastic ataxia Gene Set

Autosomal recessive spastic ataxia Gene Set

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

Spastic paraplegia 46, autosomal recessive Gene Set

Spastic paraplegia 48, autosomal recessive Gene Set

Cerebral palsy, spastic quadriplegic, 6 Gene Set

Cerebral palsy, spastic quadriplegic, 5 Gene Set

Cerebral palsy, spastic quadriplegic, 3 Gene Set

Cerebral palsy, spastic quadriplegic, 1 Gene Set

Spastic paraplegia 4, autosomal dominant Gene Set

Spastic paraplegia 18 Gene Set

Spastic paraplegia 15 Gene Set

Spastic paraplegia 13 Gene Set

Spastic paraplegia 12 Gene Set

Spastic paraplegia 54, autosomal recessive Gene Set

Spastic paraplegia 5A Gene Set

Spastic paraplegia 11, autosomal recessive Gene Set

Spastic paraplegia 57, autosomal recessive Gene Set

Spastic paraplegia 72, autosomal recessive Gene Set

Spastic paraplegia 35 Gene Set

Spastic paraplegia 44, autosomal recessive Gene Set

Spastic paraplegia 72, autosomal dominant Gene Set

Spastic paraplegia 26 Gene Set

Spastic paraplegia 55, autosomal recessive Gene Set

Spastic paraplegia 63, autosomal recessive Gene Set

Spastic paraplegia 31, autosomal dominant Gene Set

Spastic paraplegia 39 Gene Set

Spastic paraplegia 56, autosomal recessive Gene Set

Spastic paraplegia 30, autosomal recessive Gene Set

Spastic paraplegia 33, autosomal dominant Gene Set

Spastic paraplegia 8 Gene Set

Spastic paraplegia 7 Gene Set

Spastic paraplegia 6 Gene Set

Spastic paraplegia 1 Gene Set

Spastic paraplegia 3 Gene Set

Spastic paraplegia 10 Gene Set

Spastic paraplegia 45, autosomal recessive Gene Set

Infantile-onset ascending hereditary spastic paralysis Gene Set

Spastic paraplegia 42, autosomal dominant Gene Set

Spastic paraplegia 24 Gene Set

Spastic paraplegia 20, autosomal recessive Gene Set

Spastic Paraplegia 32, Autosomal Recessive Gene Set

Spastic Paraplegia 36, Autosomal Dominant Gene Set

Spastic Paraplegia 34, X-Linked Gene Set

Spastic paraplegia type 5A, recessive Gene Set

Spastic Paraplegia 7, Autosomal Recessive Gene Set

Hereditary spastic paralysis, infantile onset ascending Gene Set

Spastic paraplegia 4, autosomal dominant Gene Set

Spastic paraplegia type 5B, recessive Gene Set