spinocerebellar ataxia type 12

Summary

spinocerebellar ataxia type 12 is a developmental defect during embryogenesis^[1].

Key Facts

• spinocerebellar ataxia type 12's instance of is recorded as developmental defect during embryogenesis^[2].
• spinocerebellar ataxia type 12's instance of is recorded as rare disease^[3].
• spinocerebellar ataxia type 12's instance of is recorded as class of disease^[4].
• spinocerebellar ataxia type 12's subclass of is recorded as spinocerebellar ataxia^[5].
• spinocerebellar ataxia type 12's subclass of is recorded as autosomal dominant cerebellar ataxia type I^[6].
• spinocerebellar ataxia type 12's OMIM ID is recorded as 604326^[7].
• spinocerebellar ataxia type 12's Disease Ontology ID is recorded as DOID:0050962^[8].
• spinocerebellar ataxia type 12's Orphanet ID is recorded as 98762^[9].
• spinocerebellar ataxia type 12's NCI Thesaurus ID is recorded as C154316^[10].
• spinocerebellar ataxia type 12's genetic association is recorded as PPP2R2B^[11].
• spinocerebellar ataxia type 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050962^[12].
• spinocerebellar ataxia type 12's exact match is recorded as http://identifiers.org/doid/DOID:0050962^[13].
• spinocerebellar ataxia type 12's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98762^[14].
• spinocerebellar ataxia type 12's UMLS CUI is recorded as C1858501^[15].
• spinocerebellar ataxia type 12's ICD-10-CM is recorded as G11.2^[16].
• spinocerebellar ataxia type 12's GARD rare disease ID is recorded as 10476^[17].
• spinocerebellar ataxia type 12's on focus list of Wikimedia project is recorded as WikiProject Medicine^[18].
• spinocerebellar ataxia type 12's Mondo ID is recorded as MONDO_0011439^[19].
• spinocerebellar ataxia type 12's UniProt disease ID is recorded as DI-01075^[20].