congenital stationary night blindness 1F

Summary

DOID:0110864 - congenital stationary night blindness 1F

Disease Ontology Definition:A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25.

Synonyms: congenital stationary night blindness 1F autosomal recessive, CSNB1F

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: lrit3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014026 - congenital stationary night blindness 1F

MONDO:0014026 - congenital stationary night blindness 1F

MIM:

MIM:615058 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F

MIM:615058 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F

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)