spinocerebellar ataxia type 17
Human disease
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spinocerebellar ataxia type 17
Summary
spinocerebellar ataxia type 17 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 17's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 17's instance of is recorded as rare disease[3].
- spinocerebellar ataxia type 17's instance of is recorded as class of disease[4].
- spinocerebellar ataxia type 17's subclass of is recorded as spinocerebellar ataxia[5].
- spinocerebellar ataxia type 17's subclass of is recorded as autosomal dominant cerebellar ataxia type I[6].
- spinocerebellar ataxia type 17's subclass of is recorded as Huntington's disease-like syndrome[7].
- spinocerebellar ataxia type 17's subclass of is recorded as miscellaneous movement disorder due to genetic neurodegenerative disease[8].
- spinocerebellar ataxia type 17's MeSH descriptor ID is recorded as C564616[9].
- spinocerebellar ataxia type 17's OMIM ID is recorded as 607136[10].
- spinocerebellar ataxia type 17's Disease Ontology ID is recorded as DOID:0050967[11].
- spinocerebellar ataxia type 17's Orphanet ID is recorded as 98759[12].
- spinocerebellar ataxia type 17's NCI Thesaurus ID is recorded as C179861[13].
- spinocerebellar ataxia type 17's genetic association is recorded as TBP[14].
- spinocerebellar ataxia type 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050967[15].
- spinocerebellar ataxia type 17's exact match is recorded as http://identifiers.org/doid/DOID:0050967[16].
- spinocerebellar ataxia type 17's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98759[17].
- spinocerebellar ataxia type 17's UMLS CUI is recorded as C1846707[18].
- spinocerebellar ataxia type 17's ICD-10-CM is recorded as G11.8[19].
- spinocerebellar ataxia type 17's GARD rare disease ID is recorded as 10469[20].
- spinocerebellar ataxia type 17's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
- spinocerebellar ataxia type 17's Mondo ID is recorded as MONDO_0011781[22].
- spinocerebellar ataxia type 17's UniProt disease ID is recorded as DI-01079[23].