spinocerebellar ataxia type 29

Summary

spinocerebellar ataxia type 29 is a rare disease^[1].

Key Facts

• spinocerebellar ataxia type 29's instance of is recorded as rare disease^[2].
• spinocerebellar ataxia type 29's instance of is recorded as class of disease^[3].
• spinocerebellar ataxia type 29's subclass of is recorded as spinocerebellar ataxia^[4].
• spinocerebellar ataxia type 29's subclass of is recorded as autosomal dominant cerebellar ataxia type I^[5].
• spinocerebellar ataxia type 29's MeSH descriptor ID is recorded as C537206^[6].
• spinocerebellar ataxia type 29's OMIM ID is recorded as 117360^[7].
• spinocerebellar ataxia type 29's Disease Ontology ID is recorded as DOID:0050978^[8].
• spinocerebellar ataxia type 29's Orphanet ID is recorded as 208513^[9].
• spinocerebellar ataxia type 29's genetic association is recorded as ITPR1^[10].
• spinocerebellar ataxia type 29's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050978^[11].
• spinocerebellar ataxia type 29's exact match is recorded as http://identifiers.org/doid/DOID:0050978^[12].
• spinocerebellar ataxia type 29's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_208513^[13].
• spinocerebellar ataxia type 29's UMLS CUI is recorded as C1861732^[14].
• spinocerebellar ataxia type 29's ICD-10-CM is recorded as G11.0^[15].
• spinocerebellar ataxia type 29's GARD rare disease ID is recorded as 10480^[16].
• spinocerebellar ataxia type 29's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• spinocerebellar ataxia type 29's Mondo ID is recorded as MONDO_0007298^[18].
• spinocerebellar ataxia type 29's UniProt disease ID is recorded as DI-03660^[19].