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Oculocutaneous albinism type 1B

MONDO:0011749

Oculocutaneous albinism type 1B (OCA1B) is a type of OCA1 characterized by skin and hair hypopigmentation, nystagmus, reduced iris and retinal pigment and misrouting of the optic nerves.

Also known as: OCA1B, Yellow oculocutaneous albinism, albinism, Yellow mutant type, oculocutaneous albinism, Amish type, platinum oculocutaneous albinism, Oca1-Ts, Yellow albinism, Yellow mutant albinism

32 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Skin disorder (123) Inborn errors of metabolism (42) Human disease (14) Skin pigmentation disorder (11) Hereditary skin disorder (5) Autosomal recessive disease (4) Inborn disorder of amino acid metabolism (4)

Trials to join now! 17 Not yet recruiting 4 Not yet finished but already full! 4 Completed 6 Terminated 1

VR headsets tested as a possible treatment for blindness

Disease control Terminated

This study tested whether using a virtual reality headset for one-hour sessions could help regenerate damaged optic nerves and improve vision in people with glaucoma or other retinal diseases. The idea came from promising results in rodents. However, the trial was terminated earl…

Phase: NA • Sponsor: Stanford University • Aim: Disease control

Last updated Jun 27, 2026 08:03 UTC