Charlevoix-Saguenay spastic ataxia
neurological disease
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Summary
Charlevoix-Saguenay spastic ataxia is a rare disease[1]. It draws 137 Wikipedia views per month (rare disease category, ranking #135 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: spastic ataxia[4], autosomal recessive cerebellar ataxia[5], autosomal recessive spastic ataxia[6], developmental defect during embryogenesis[7]
- NCI Thesaurus ID: C154614[8]
- Health specialty: neurology[9]
- Genetic association: SACS[10]
- Age of onset: juvenile onset[11], adult onset[12], childhood onset[13], infantile onset[14]
- Exact match: http://purl.obolibrary.org/obo/DOID_0050946[15], http://identifiers.org/doid/DOID:0050946[16]
- On focus list of Wikimedia project: WikiProject Medicine[17]
- Has phenotype: arachnoid cyst[18], foot deformity[19], erectile dysfunction[20]
- P14914: D00098[21]
Why It Matters
Charlevoix-Saguenay spastic ataxia is known by 17 alternative names across languages and contexts.[22]