spinocerebellar ataxia type 37
Spinocerebellar ataxia type 37 (SCA37) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1; see this term), characterized by a cerebellar syndrome along with altered vertical eye movements
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spinocerebellar ataxia type 37
Summary
spinocerebellar ataxia type 37 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 37's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 37's instance of is recorded as class of disease[3].
- spinocerebellar ataxia type 37's subclass of is recorded as spinocerebellar ataxia[4].
- spinocerebellar ataxia type 37's subclass of is recorded as autosomal dominant cerebellar ataxia type I[5].
- spinocerebellar ataxia type 37's OMIM ID is recorded as 615945[6].
- spinocerebellar ataxia type 37's Disease Ontology ID is recorded as DOID:0050984[7].
- spinocerebellar ataxia type 37's Orphanet ID is recorded as 363710[8].
- spinocerebellar ataxia type 37's genetic association is recorded as DAB1[9].
- spinocerebellar ataxia type 37's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050984[10].
- spinocerebellar ataxia type 37's exact match is recorded as http://identifiers.org/doid/DOID:0050984[11].
- spinocerebellar ataxia type 37's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_363710[12].
- spinocerebellar ataxia type 37's UMLS CUI is recorded as C3889636[13].
- spinocerebellar ataxia type 37's ICD-10-CM is recorded as G11.8[14].
- spinocerebellar ataxia type 37's GARD rare disease ID is recorded as 12368[15].
- spinocerebellar ataxia type 37's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- spinocerebellar ataxia type 37's Mondo ID is recorded as MONDO_0014410[17].
- spinocerebellar ataxia type 37's UniProt disease ID is recorded as DI-05050[18].