All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05323 MYP myopia (MYP) - - 20 17 ARR3, PLOD1, SLC39A5, ZNF644 - -
05731 MYP26 myopia, type 26, X-linked, female-limited (MYP26) 301010 XL - - ARR3 - -
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