OBO ID: DOID:0111614
Term Name: autosomal recessive spinocerebellar ataxia 22 Search Ontology:
Synonyms:
  • SCAR22
Definition: An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2. https://www.ncbi.nlm.nih.gov/pubmed/26157035
References:
Ontology: Human Disease   ( DOID:0111614 )
OTHER autosomal recessive spinocerebellar ataxia 22 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VWA3B ?Spinocerebellar ataxia, autosomal recessive 22
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None