|
DOID:13912 - acquired color blindness
Disease Ontology Definition:n_a
Synonyms: acquired color vision deficiencies, acquired color vision deficiency, acquired colour blindness, acquired colour vision deficiencies, acquired colour vision deficiency,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0001828 - acquired color blindness |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
color blindness (is_a)