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DOID:0050632 - oculocutaneous albinism
Disease Ontology Definition:A syndrome characterized by abnormal pigmentation of the skin, hair and eyes.
Synonyms:
Xenbase Genes
:
slc24a5,
slc45a2,
lrmda,
tyr,
oca2,
tyrp1,
mc1r,
abcc6
| MONDO:0018910 - oculocutaneous albinism |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
syndrome (is_a)