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DOID:0110868 - congenital stationary night blindness 1D
Disease Ontology Definition:A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SLC24A1 gene on chromosome 15q22.
Synonyms: CSNB1D, congenital stationary night blindness 1D autosomal recessive,
Xenbase Genes : slc24a1
MONDO:0013450 - congenital stationary night blindness 1D |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital stationary night blindness (is_a)