|OBO ID: DOID:0110869|
|Term Name:||congenital stationary night blindness 1E||Search Ontology:|
|Definition:||A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GPR179 gene on chromosome 17q12. https://www.ncbi.nlm.nih.gov/pubmed/22325361|
|Ontology:||Human Disease (DOID:0110869)|
|is a type of:||
OTHER congenital stationary night blindness 1E PAGES
PHENOTYPE No data available
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.