Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
OMIM:617238 - MYOPIA 25, AUTOSOMAL DOMINANT; MYP25


Xenbase Genes: p4ha2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014982 - myopia 25, autosomal dominant