oculocutaneous albinism

MeSH: D016115ORPHA: 55

Overview

autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

D016115

Orphanet Code

ORPHA:55
oculocutaneous albinism
MeSHD016115
OrphanetORPHA:55
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO