Oculocutaneous albinism type 1 [Supplementary Concept]
A type of oculocutaneous albinism caused by specific mutations in the TYR gene. OMIM: 606933
Date introduced: August 25, 2010
MeSH Unique ID: C537728
Heading Mapped to:
Entry Terms:
- Albinism 1
- Oculocutaneous Albinism, Type I
- Albinism I
- Albinism, Oculocutaneous, Type IA
- Oculocutaneous albinism type 1A
- Oculocutaneous albinism, tyrosinase negative
- Oculocutaneous Albinism, Tyrosinase-Negative