bn:04875039n
Noun Concept
EN
oculocutaneous albinism type 2  OCA2  Oculocutaneous Albinism, Tyrosinase-Positive  oculocutaneous albinism type II
EN
Oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13 Wikidata
Definitions
Relations
Sources
EN
Oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13 Wikidata