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myopia 21, autosomal dominant

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any myopia (disease) in which the cause of the disease is a mutation in the ZNF644 gene.
Uniprot Description A refractive error of the eye, in which parallel rays from a distant object come to focus in front of the retina, vision being better for near objects than for far.
Mondo Term and Equivalent IDs
MONDO:0013604:  myopia 21, autosomal dominant
UMLS:C3279997: