Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (1)
OMIM:203100 - ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A


Xenbase Genes: tyr

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008745 - oculocutaneous albinism type 1A
MONDO:0018135 - oculocutaneous albinism type 1

Disease Ontology (DO):
DOID:0050632 - oculocutaneous albinism
DOID:0070094 - oculocutaneous albinism type IA