spinocerebellar ataxia type 19/22
Human disease
Press Enter · cited answer in seconds
0 sources
spinocerebellar ataxia type 19/22
Summary
spinocerebellar ataxia type 19/22 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 19/22's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 19/22's instance of is recorded as rare disease[3].
- spinocerebellar ataxia type 19/22's instance of is recorded as class of disease[4].
- spinocerebellar ataxia type 19/22 is a type of spinocerebellar ataxia[5].
- spinocerebellar ataxia type 19/22 is a type of autosomal dominant cerebellar ataxia type I[6].
- spinocerebellar ataxia type 19/22's NCI Thesaurus ID is recorded as C163756[7].
- spinocerebellar ataxia type 19/22's genetic association is recorded as KCND3[8].
- spinocerebellar ataxia type 19/22's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050970[9].
- spinocerebellar ataxia type 19/22's exact match is recorded as http://identifiers.org/doid/DOID:0050970[10].
- spinocerebellar ataxia type 19/22's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101107[11].
- spinocerebellar ataxia type 19/22's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98772[12].
- spinocerebellar ataxia type 19/22's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].