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oculocutaneous albinism type 2 (OCA2)
disorder of pigmentation in the skin, hair, & eyes
Epidemiology:
- most prevalent type of albinism throughout the world
Genetics:
- autosomal recessive
- associated with defects in OCA2
Clinical manifestations:
- typically somewhat less severe than in those with tyrosinase-deficient oculocutaneous albinism type 1
- several forms with different severity
General
oculocutaneous albinism
Database Correlations
OMIM 203200
References
OMIM :accession 203200