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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: CSNB1C, congenital stationary night blindness 1C autosomal recessive,
Xenbase Genes : trpm1
MONDO:0013183 - congenital stationary night blindness 1C |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee