hereditary night blindness

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Summary

Literature (0)

DOID:8498 - hereditary night blindness

Disease Ontology Definition:n_a

Synonyms: Congenital night blindness, Oguchi's disease

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

: trpm1, grm6, nyx, sag, gnb3, pde6b, rho, slc24a1, gpr179, gnat1, grk1, cacna1f, cabp4, lrit3, rho.2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0004587 - obsolete hereditary night blindness

MONDO:0004587 - obsolete hereditary night blindness

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): night blindness (is_a)