/myopia 25, autosomal dominant

myopia 25, autosomal dominant

MONDO:0014982

Also Known As

MYP25P4HA2 myopia (disease)myopia (disease) caused by mutation in P4HA2myopia 25, autosomal dominantmyopia 25, autosomal dominant; MYP25

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

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

degenerative myopia

MONDO:0001383

myopia 2, autosomal dominant

MONDO:0008053

myopia 18, autosomal recessive

MONDO:0009713

myopia 13, X-linked

MONDO:0010377

myopia 1, X-linked

MONDO:0010685

myopia 3, autosomal dominant

MONDO:0011300