|
DOID:0110869 - congenital stationary night blindness 1E
Disease 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.
Synonyms: CSNB1E, congenital stationary night blindness 1E autosomal recessive,
Xenbase Genes
:
gpr179
| MONDO:0013807 - congenital stationary night blindness 1E |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital stationary night blindness (is_a)