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Albinism

MONDO:0043209

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

Also known as: albinism

6 clinical trials for this condition and its sub-types, 6 tagged with Albinism itself.

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Where it sits in the disease tree

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Part of

↑ Inborn disorder of amino acid metabolism (159)

Sub-types of Albinism

X-linked recessive ocular albinism 0 trials
Albinism-hearing loss syndrome 0 trials

Including sub-types (6) Tagged with Albinism (6)

Trials to join now! 4 Not yet recruiting 1 Completed 1

New DNA reader could crack unsolved rare disease cases

Knowledge-focused Not yet recruiting

This study tests a new DNA sequencing method that reads long stretches of DNA to find hidden genetic changes causing rare diseases like albinism and intellectual disability. Researchers will analyze stored blood or DNA from 150 patients who haven't gotten a clear diagnosis yet. T…

Sponsor: University Hospital, Bordeaux • Aim: Knowledge-focused

Last updated Jun 27, 2026 09:03 UTC