OBO ID: DOID:0080057
Term Name: autosomal recessive spinocerebellar ataxia 15 Search Ontology:
Synonyms:
  • SCAR15
Definition: An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the RUBCN gene on chromosome 3q29. https://www.ncbi.nlm.nih.gov/pubmed/20826435
References:
Ontology: Human Disease   ( DOID:0080057 )
OTHER autosomal recessive spinocerebellar ataxia 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RUBCN Spinocerebellar ataxia, autosomal recessive 15 615705
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None