All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00046 lactase def. lactase deficiency, congenital 223000 AR - - LCT - -
00047 lactose intol. lactose intolerance (lactase persistence/nonpersistence) 223100 AD 12 12 LCT, MCM6 - -
00979 PTRPLS Peters-plus syndrome 261540 AR 32 20 B3GLCT - -
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