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
03799 LEPD obesity, severe, due to leptin deficiency (LEPD) 614962 AR - - LEP - autosomal reessive
03800 LEPRD deficiency, leptin receptor 614963 AR - - LEPR - -
03595 MCVD myopia, high, with cataract and vitreoretinal degeneration 614292 AR 1 - LEPREL1 - -
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