Version: 8.0.0
Date: Tue Jan 28 2025
oculocutaneous albinism type II
DOID:0070096
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

oculocutaneous albinism type II

Definition
An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the OCA2 gene on chromosome 15q12-q13.
Synonyms
  • OCA2
  • Oculocutaneous Albinism, Tyrosinase-Positive
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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