All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00204 AD Alzheimer disease (AD) 104300 - - - A2M, ACE, APBB2, APP, BLMH, HFE, MPO, NOS3, PAXIP1, PLAU, PRNP, SORL1 - -
00411 HFE-1 hemochromatosis, type 1 (HFE-1) 235200 - - - BMP2, HFE - -
00357 HFE-2A hemochromatosis, juvenile, type 2A (HFE-2A) 602390 - - - HFE2 - -
03168 MVCD-7 microvascular complications of diabetes, type 7 (MVCD-7) 612635 - - - HFE - -
00415 PCT porphyria cutanea tarda (PCT) 176100 - - - HFE, UROD - -
03576 TFQTL-2 transferrin serum level, quantitative trait locus 2 (TFQTL-2) 614193 - - - HFE - -
00416 VP porphyria, variagated (VP) 176200 - - - HFE, PPOX - -
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