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Diseases / Metabolic disease/ Amino acid metabolism disease/ Inborn disorder of amino acid metabolism

Albinism

rare

A congenital disorder characterized by partial or complete absence of melanin pigment in the eyes, hair, or skin.

Identifiers: MONDO:0043209
Part of: Inborn disorder of amino acid metabolism

Subtypes

All diseases Rare only

Disease

X-linked recessive ocular albinism MONDO:0021019
Albinism-hearing loss syndrome MONDO:0010403

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