Myopia 22, Autosomal Dominant (MYP22)

Alias:

Myp22

Myopia, Autosomal Dominant, Type 22

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Myopia 22, Autosomal Dominant, is also known as myp22. An important gene associated with Myopia 22, Autosomal Dominant is PRIMPOL (Primase And DNA Directed Polymerase). Affiliated tissues include retina and eye, and related phenotypes are high myopia and reduced visual acuity

Related ID：

MALACARDS：MYP075

OMIM：615420

MESH：D009216