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DOID:0110865 - congenital stationary night blindness 1B
Disease Ontology Definition:A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35.
Synonyms: CSNB1B, autosomal recessive complete congenital stationary night blindness, congenital stationary night blindness 1B autosomal recessive,
Xenbase Genes
:
grm6
| MONDO:0009758 - congenital stationary night blindness 1B |
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)