DISEASES

Disease-gene associations mined from literature

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Human genes for oculocutaneous albinism type II

Oculocutaneous albinism type II [DOID:0070096]

An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13.

Synonyms:  oculocutaneous albinism type II,  DOID:0070096,  oculocutaneous albinism type IIs,  Oculocutaneous Albinism, Tyrosinase-Positive,  Oculocutaneous Albinism TyrosinasePositive ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.