spinocerebellar ataxia 46
human disease
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spinocerebellar ataxia 46
Summary
spinocerebellar ataxia 46 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia 46's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia 46's instance of is recorded as class of disease[3].
- spinocerebellar ataxia 46's subclass of is recorded as spinocerebellar ataxia[4].
- spinocerebellar ataxia 46's OMIM ID is recorded as 617770[5].
- spinocerebellar ataxia 46's Disease Ontology ID is recorded as DOID:0080288[6].
- spinocerebellar ataxia 46's genetic association is recorded as PLD3[7].
- spinocerebellar ataxia 46's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080288[8].
- spinocerebellar ataxia 46's exact match is recorded as http://identifiers.org/doid/DOID:0080288[9].
- spinocerebellar ataxia 46's UMLS CUI is recorded as C4540404[10].
- spinocerebellar ataxia 46's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- spinocerebellar ataxia 46's Mondo ID is recorded as MONDO_0033481[12].
- spinocerebellar ataxia 46's UniProt disease ID is recorded as DI-05144[13].