OBO ID: DOID:0050999
Term Name: autosomal recessive spinocerebellar ataxia 10 Search Ontology:
Synonyms:
  • SCAR10
Definition: An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene. https://www.omim.org/entry/613728
References:
Ontology: Human Disease   (DOID:0050999)
OTHER autosomal recessive spinocerebellar ataxia 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ANO10 Spinocerebellar ataxia, autosomal recessive 10 613728
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None