/myopia 21, autosomal dominant

myopia 21, autosomal dominant

MONDO:0013604

Also Known As

ZNF644 myopia (disease)myopia (disease) caused by mutation in ZNF644myopia 21, autosomal dominantMYP21

Any myopia (disease) in which the cause of the disease is a mutation in the ZNF644 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