Search Ontology:
Human Disease

cerebellar ataxia type 41

Term ID
DOID:0111744
Synonyms
  • SCA41
Definition
An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the TRPC3 gene on chromosome 4q27. https://www.ncbi.nlm.nih.gov/pubmed/25477146
References
Ontology
Human Disease   ( DOID:0111744 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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