Charlevoix-Saguenay spastic ataxia
neurological disease
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Charlevoix-Saguenay spastic ataxia
Summary
Charlevoix-Saguenay spastic ataxia is a developmental defect during embryogenesis[1].
Key Facts
- Charlevoix-Saguenay spastic ataxia's instance of is recorded as developmental defect during embryogenesis[2].
- Charlevoix-Saguenay spastic ataxia's instance of is recorded as rare disease[3].
- Charlevoix-Saguenay spastic ataxia's instance of is recorded as class of disease[4].
- Charlevoix-Saguenay spastic ataxia is a type of spastic ataxia[5].
- Charlevoix-Saguenay spastic ataxia is a type of autosomal recessive cerebellar ataxia[6].
- Charlevoix-Saguenay spastic ataxia is a type of autosomal recessive spastic ataxia[7].
- Charlevoix-Saguenay spastic ataxia's NCI Thesaurus ID is recorded as C154614[8].
- Charlevoix-Saguenay spastic ataxia's health specialty is recorded as neurology[9].
- Charlevoix-Saguenay spastic ataxia's genetic association is recorded as SACS[10].
- Charlevoix-Saguenay spastic ataxia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050946[11].
- Charlevoix-Saguenay spastic ataxia's exact match is recorded as http://identifiers.org/doid/DOID:0050946[12].
- Charlevoix-Saguenay spastic ataxia's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].