achromatopsia 4

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Summary

Literature (0)

DOID:0110010 - achromatopsia 4

Disease Ontology Definition:An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the GNAT2 gene on chromosome 1p13.

Synonyms: ACHM4

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

: gnat2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013465 - achromatopsia 4

MONDO:0013465 - achromatopsia 4

MIM:

MIM:613856 - ACHROMATOPSIA 4; ACHM4

MIM:613856 - ACHROMATOPSIA 4; ACHM4

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

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

Parent(s): achromatopsia (is_a)