Cayman type cerebellar ataxia
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Summary
Cayman type cerebellar ataxia is a developmental defect during embryogenesis[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- Instance of: rare disease[3], class of disease[4]
- Subclass of: cerebellar ataxia[5], autosomal recessive congenital cerebellar ataxia[6], monogenic disease[7], autosomal recessive cerebellar ataxia[8]
- Health specialty: neurology[9]
- Genetic association: ATCAY[10]
- Exact match: http://purl.obolibrary.org/obo/DOID_0060694[11], http://identifiers.org/doid/DOID:0060694[12]
- On focus list of Wikimedia project: WikiProject Medicine[13]