spinocerebellar ataxia type 31
Human disease
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Summary
spinocerebellar ataxia type 31 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: spinocerebellar ataxia[4], autosomal dominant cerebellar ataxia type III[5], developmental defect during embryogenesis[6]
- NCI Thesaurus ID: C176901[7]
- Genetic association: BEAN1[8]
- Age of onset: juvenile onset[9], adult onset[10], childhood onset[11], late onset[12]
- Exact match: http://purl.obolibrary.org/obo/DOID_0050980[13], http://identifiers.org/doid/DOID:0050980[14], http://www.orpha.net/ORDO/Orphanet_217012[15]
- On focus list of Wikimedia project: WikiProject Medicine[16]
- Has phenotype: dysarthria[17], cerebellar atrophy[18], ataxia[19], pathologic nystagmus[20], hyporeflexia[21], deafness[22], sensorineural hearing loss[23], spasticity[24], tremor[25], abnormal reflex[26], Q141815185[27], Q141815619[28]
- P14914: D217012[29]