spinocerebellar ataxia type 42

Summary

spinocerebellar ataxia type 42 is a developmental defect during embryogenesis^[1].

Key Facts

• spinocerebellar ataxia type 42's instance of is recorded as developmental defect during embryogenesis^[2].
• spinocerebellar ataxia type 42's instance of is recorded as rare disease^[3].
• spinocerebellar ataxia type 42's instance of is recorded as class of disease^[4].
• spinocerebellar ataxia type 42's subclass of is recorded as autosomal dominant cerebellar ataxia type III^[5].
• spinocerebellar ataxia type 42's subclass of is recorded as spinocerebellar ataxia^[6].
• spinocerebellar ataxia type 42's OMIM ID is recorded as 616795^[7].
• spinocerebellar ataxia type 42's Disease Ontology ID is recorded as DOID:0111742^[8].
• spinocerebellar ataxia type 42's Orphanet ID is recorded as 458803^[9].
• spinocerebellar ataxia type 42's NCI Thesaurus ID is recorded as C171269^[10].
• spinocerebellar ataxia type 42's genetic association is recorded as CACNA1G^[11].
• spinocerebellar ataxia type 42's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_458803^[12].
• spinocerebellar ataxia type 42's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111742^[13].
• spinocerebellar ataxia type 42's exact match is recorded as http://identifiers.org/doid/DOID:0111742^[14].
• spinocerebellar ataxia type 42's UMLS CUI is recorded as C4225205^[15].
• spinocerebellar ataxia type 42's ICD-10-CM is recorded as G11.8^[16].
• spinocerebellar ataxia type 42's Mondo ID is recorded as MONDO_0014776^[17].
• spinocerebellar ataxia type 42's UniProt disease ID is recorded as DI-04644^[18].
• spinocerebellar ataxia type 42's Experimental Factor Ontology ID is recorded as 0009059^[19].