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oculocutaneous albinism type 3 (OCA3)
Genetics:
- associated with defects in TYRP1
Clinical manifestations:
- form of albinism with only moderate reduction of pigment
- individuals with OCA3 are recognized by their reddish skin & hair color
General
oculocutaneous albinism
Database Correlations
OMIM 203290
References
OMIM :accession 203290