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Autosomal recessive ocular albinism

MONDO:0040653

Autosomal recessive form of ocular albinism (disease).

Also known as: autosomal recessive ocular albinism, autosomal recessive ocular albinism (disease), ocular albinism (disease), autosomal recessive, AROA

1 clinical trial for this condition and its sub-types.

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Sub-types

Oculocutaneous albinism type 1A (1) Oculocutaneous albinism type 1B (0)

Broader categories

Disease (717) Metabolic disease (241) Hereditary disease (188) Inborn errors of metabolism (47) Human disease (15) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Ocular albinism (1) Autosomal genetic disease (0)
Trials to join now! 1
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  • Gene therapy injection aims to restore pigment in Children's eyes

    Disease control Recruiting now

    This early-phase trial tests a single injection of JWK010 gene therapy in 18 children aged 5 to 12 with oculocutaneous albinism type 1 (OCA1). OCA1 is caused by a gene change that prevents the body from making pigment, leading to vision problems and light sensitivity. The therapy…

    Early phase 1 • Sponsor: West China Hospital • Aim: Disease control

    Last updated Jun 27, 2026 08:10 UTC

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