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Summary Literature (0)
DOID:0110867 - congenital stationary night blindness 1C

Disease Ontology Definition:A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14.

Synonyms: congenital stationary night blindness 1C autosomal recessive, CSNB1C

Xenbase Genes : trpm1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013183 - congenital stationary night blindness 1C

MIM:
MIM:613216 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C

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)