cerebellar ataxia type 43
human disease
Press Enter · cited answer in seconds
0 sources
cerebellar ataxia type 43
Summary
cerebellar ataxia type 43 is a developmental defect during embryogenesis[1].
Key Facts
- cerebellar ataxia type 43's instance of is recorded as developmental defect during embryogenesis[2].
- cerebellar ataxia type 43's instance of is recorded as rare disease[3].
- cerebellar ataxia type 43's instance of is recorded as class of disease[4].
- cerebellar ataxia type 43 is a type of spinocerebellar ataxia[5].
- cerebellar ataxia type 43's genetic association is recorded as MME[6].
- cerebellar ataxia type 43's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111745[7].
- cerebellar ataxia type 43's exact match is recorded as http://identifiers.org/doid/DOID:0111745[8].