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's subclass of is recorded as spinocerebellar ataxia^[5].
• cerebellar ataxia type 43's OMIM ID is recorded as 617018^[6].
• cerebellar ataxia type 43's Disease Ontology ID is recorded as DOID:0111745^[7].
• cerebellar ataxia type 43's Orphanet ID is recorded as 497764^[8].
• cerebellar ataxia type 43's genetic association is recorded as MME^[9].
• cerebellar ataxia type 43's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111745^[10].
• cerebellar ataxia type 43's exact match is recorded as http://identifiers.org/doid/DOID:0111745^[11].
• cerebellar ataxia type 43's UMLS CUI is recorded as C4310763^[12].
• cerebellar ataxia type 43's Mondo ID is recorded as MONDO_0014867^[13].
• cerebellar ataxia type 43's UniProt disease ID is recorded as DI-04796^[14].