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
03507 CPHD6 hormone deficiency, pituitary, combined, type 6 613986 AD - - OTX2 - -
02903 MCOPS5 microphthalmia, syndromic, type 5 (dystrophy, retinal, early onset) 610125 AD 1 1 OTX2 - -
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