spinocerebellar ataxia type 1
Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities
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spinocerebellar ataxia type 1
Summary
spinocerebellar ataxia type 1 is a developmental defect during embryogenesis[1]. It draws 10 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).[2]
Key Facts
- spinocerebellar ataxia type 1's instance of is recorded as developmental defect during embryogenesis[3].
- spinocerebellar ataxia type 1's instance of is recorded as rare disease[4].
- spinocerebellar ataxia type 1's instance of is recorded as class of disease[5].
- spinocerebellar ataxia type 1's subclass of is recorded as spinocerebellar ataxia[6].
- spinocerebellar ataxia type 1's subclass of is recorded as Huntington's disease-like syndrome[7].
- spinocerebellar ataxia type 1's subclass of is recorded as autosomal dominant cerebellar ataxia type I[8].
- spinocerebellar ataxia type 1's OMIM ID is recorded as 164400[9].
- spinocerebellar ataxia type 1's Disease Ontology ID is recorded as DOID:0050954[10].
- spinocerebellar ataxia type 1's Orphanet ID is recorded as 98755[11].
- spinocerebellar ataxia type 1's NCI Thesaurus ID is recorded as C129982[12].
- spinocerebellar ataxia type 1's genetic association is recorded as ATXN1[13].
- spinocerebellar ataxia type 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050954[14].
- spinocerebellar ataxia type 1's exact match is recorded as http://identifiers.org/doid/DOID:0050954[15].
- spinocerebellar ataxia type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98755[16].
- spinocerebellar ataxia type 1's UMLS CUI is recorded as C0752120[17].
- spinocerebellar ataxia type 1's ICD-10-CM is recorded as G11.8[18].
- spinocerebellar ataxia type 1's GARD rare disease ID is recorded as 4071[19].
- spinocerebellar ataxia type 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- spinocerebellar ataxia type 1's Mondo ID is recorded as MONDO_0008119[21].
- spinocerebellar ataxia type 1's Genetics Home Reference Conditions ID is recorded as spinocerebellar-ataxia-type-1[22].
- spinocerebellar ataxia type 1's KBpedia ID is recorded as SpinocerebellarAtaxiaType1[23].
- spinocerebellar ataxia type 1's WikiProjectMed ID is recorded as Spinocerebellar ataxia type 1[24].
- spinocerebellar ataxia type 1's UniProt disease ID is recorded as DI-01066[25].
Why It Matters
spinocerebellar ataxia type 1 draws 10 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).[2]