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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: CSNB1F, congenital stationary night blindness 1F autosomal recessive,
Xenbase Genes : lrit3
MONDO:0014026 - congenital stationary night blindness 1F |
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)