spinocerebellar ataxia 44
human disease
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spinocerebellar ataxia 44
Summary
spinocerebellar ataxia 44 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia 44's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia 44's instance of is recorded as class of disease[3].
- spinocerebellar ataxia 44's subclass of is recorded as spinocerebellar ataxia[4].
- spinocerebellar ataxia 44's OMIM ID is recorded as 617691[5].
- spinocerebellar ataxia 44's Disease Ontology ID is recorded as DOID:0080286[6].
- spinocerebellar ataxia 44's genetic association is recorded as GRM1[7].
- spinocerebellar ataxia 44's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080286[8].
- spinocerebellar ataxia 44's exact match is recorded as http://identifiers.org/doid/DOID:0080286[9].
- spinocerebellar ataxia 44's UMLS CUI is recorded as C4521563[10].
- spinocerebellar ataxia 44's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- spinocerebellar ataxia 44's Mondo ID is recorded as MONDO_0033479[12].
- spinocerebellar ataxia 44's UniProt disease ID is recorded as DI-05091[13].