spinocerebellar ataxia type 23

Summary

spinocerebellar ataxia type 23 is a developmental defect during embryogenesis^[1].

Key Facts

• spinocerebellar ataxia type 23's instance of is recorded as developmental defect during embryogenesis^[2].
• spinocerebellar ataxia type 23's instance of is recorded as rare disease^[3].
• spinocerebellar ataxia type 23's instance of is recorded as class of disease^[4].
• spinocerebellar ataxia type 23's subclass of is recorded as spinocerebellar ataxia^[5].
• spinocerebellar ataxia type 23's subclass of is recorded as autosomal dominant cerebellar ataxia type I^[6].
• spinocerebellar ataxia type 23's MeSH descriptor ID is recorded as C537201^[7].
• spinocerebellar ataxia type 23's OMIM ID is recorded as 610245^[8].
• spinocerebellar ataxia type 23's Disease Ontology ID is recorded as DOID:0050973^[9].
• spinocerebellar ataxia type 23's Orphanet ID is recorded as 101108^[10].
• spinocerebellar ataxia type 23's genetic association is recorded as PDYN^[11].
• spinocerebellar ataxia type 23's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050973^[12].
• spinocerebellar ataxia type 23's exact match is recorded as http://identifiers.org/doid/DOID:0050973^[13].
• spinocerebellar ataxia type 23's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101108^[14].
• spinocerebellar ataxia type 23's UMLS CUI is recorded as C1853250^[15].
• spinocerebellar ataxia type 23's ICD-10-CM is recorded as G11.2^[16].
• spinocerebellar ataxia type 23's GARD rare disease ID is recorded as 9950^[17].
• spinocerebellar ataxia type 23's on focus list of Wikimedia project is recorded as WikiProject Medicine^[18].
• spinocerebellar ataxia type 23's Mondo ID is recorded as MONDO_0012449^[19].
• spinocerebellar ataxia type 23's UniProt disease ID is recorded as DI-02949^[20].