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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

Hidden eye condition linked to albinism genes in healthy people?

Knowledge-focused Completed

This study looked at 20 adults who have a flat spot in the center of their retina (fovea plana) but no known albinism or vision problems. Researchers used eye scans and genetic tests to see if these people carry gene changes linked to albinism. The goal was to better understand w…

Sponsor: Fondation Ophtalmologique Adolphe de Rothschild • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:09 UTC