Oculocutaneous albinism, TYR-related, rabbit

MONDO:1012598

Oculocutaneous albinism that occurs in rabbits due to a mutation in the TYR gene.

Also known as: coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related in Oryctolagus cuniculus (rabbit)

0 clinical trials for this condition and its sub-types, 0 tagged with Oculocutaneous albinism, TYR-related, rabbit itself.

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