OBO ID: DOID:0050985
Term Name: spinocerebellar ataxia type 38 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and nystagmus, presenting in mid-adulthood, and has_material_basis_in mutation to the ELOVL5 gene. https://www.omim.org/entry/615957
References:
Ontology: Human Disease   (DOID:0050985)
OTHER spinocerebellar ataxia type 38 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ELOVL5 Spinocerebellar ataxia 38 615957
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None