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Summary Literature (0)
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: autosomal recessive complete congenital stationary night blindness, congenital stationary night blindness 1B autosomal recessive, CSNB1B

Xenbase Genes : grm6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009758 - abdominal ganglion

MIM:
MIM:257270 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), congenital stationary night blindness (is_a)