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
D016115Orphanet Code
ORPHA:55oculocutaneous albinism
| MeSH | D016115 |
| Orphanet | ORPHA:55 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO