Myopia 25, autosomal dominant

MONDO:0014982

Any myopia (disease) in which the cause of the disease is a mutation in the P4HA2 gene.

Also known as: MYP25, P4HA2 myopia (disease), myopia (disease) caused by mutation in P4HA2, myopia 25, autosomal dominant, myopia 25, autosomal dominant; MYP25

10 clinical trials for this condition and its sub-types, 0 tagged with Myopia 25, autosomal dominant itself.

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Where it sits in the disease tree

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Including sub-types (10) Tagged with Myopia 25, autosomal dominant (0)

Trials to join now! 2 Not yet recruiting 3 Not yet finished but already full! 1 Completed 4

AI eye test: could a computer replace your eye doctor?

Diagnosis By invitation only

This study compares a new AI system, called AEYE, against a human eye doctor in diagnosing keratoconus and deciding who is eligible for laser vision correction. The AI analyzes patient history, eye scans, and other data to make its recommendations. Researchers will check if the A…

Sponsor: Hazem Yassin Clinics • Aim: Diagnosis

Last updated Jun 26, 2026 17:00 UTC

Myopia 25, autosomal dominant

Where it sits in the disease tree

AI eye test: could a computer replace your eye doctor?