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Disease Ontology Browser
achromatopsia (DOID:13911)
Alliance: disease page
Synonyms: ACHM; Monochromatism
Alt IDs: ICD10CM:H53.51, ICD9CM:368.54, MESH:D003117, NCI:C84528, ORDO:49382, UMLS_CUI:C0152200
Definition: A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance.

Disease References using Mouse Models (14)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory