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]. It draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- Charlevoix-Saguenay spastic ataxia's instance of is recorded as developmental defect during embryogenesis[3].
- Charlevoix-Saguenay spastic ataxia's instance of is recorded as rare disease[4].
- Charlevoix-Saguenay spastic ataxia's instance of is recorded as class of disease[5].
- Charlevoix-Saguenay spastic ataxia's subclass of is recorded as spastic ataxia[6].
- Charlevoix-Saguenay spastic ataxia's subclass of is recorded as autosomal recessive cerebellar ataxia[7].
- Charlevoix-Saguenay spastic ataxia's subclass of is recorded as autosomal recessive spastic ataxia[8].
- Charlevoix-Saguenay spastic ataxia's MeSH descriptor ID is recorded as C536787[9].
- Charlevoix-Saguenay spastic ataxia's OMIM ID is recorded as 270550[10].
- Charlevoix-Saguenay spastic ataxia's ICD-10 ID is recorded as G11.1[11].
- Charlevoix-Saguenay spastic ataxia's DiseasesDB is recorded as 33522[12].
- Charlevoix-Saguenay spastic ataxia's KEGG ID is recorded as H01170[13].
- Charlevoix-Saguenay spastic ataxia's Disease Ontology ID is recorded as DOID:0050946[14].
- Charlevoix-Saguenay spastic ataxia's Orphanet ID is recorded as 98[15].
- Charlevoix-Saguenay spastic ataxia's NCI Thesaurus ID is recorded as C154614[16].
- Charlevoix-Saguenay spastic ataxia's health specialty is recorded as neurology[17].
- Charlevoix-Saguenay spastic ataxia's genetic association is recorded as SACS[18].
- Charlevoix-Saguenay spastic ataxia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050946[19].
- Charlevoix-Saguenay spastic ataxia's exact match is recorded as http://identifiers.org/doid/DOID:0050946[20].
- Charlevoix-Saguenay spastic ataxia's UMLS CUI is recorded as C1849140[21].
- Charlevoix-Saguenay spastic ataxia's ICD-10-CM is recorded as G11.1[22].
- Charlevoix-Saguenay spastic ataxia's GARD rare disease ID is recorded as 4910[23].
- Charlevoix-Saguenay spastic ataxia's on focus list of Wikimedia project is recorded as WikiProject Medicine[24].
- Charlevoix-Saguenay spastic ataxia's Mondo ID is recorded as MONDO_0010041[25].
- Charlevoix-Saguenay spastic ataxia's Genetics Home Reference Conditions ID is recorded as autosomal-recessive-spastic-ataxia-of-charlevoix-saguenay[26].
- Charlevoix-Saguenay spastic ataxia's UniProt disease ID is recorded as DI-01259[27].
Why It Matters
Charlevoix-Saguenay spastic ataxia draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]