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 AD 697 164 A2M, ACE, APBB2, APP, BLMH, HFE, MPO, NOS3, PAXIP1, PLAU, PRNP, SORL1 - -
00411 HFE1 hemochromatosis, type 1 (HFE-1) 235200 AR 40 40 BMP2, HFE - -
00357 HFE2A hemochromatosis, juvenile, type 2A (HFE-2A) 602390 AR - - HFE2 - -
03168 MVCD7 microvascular complications of diabetes, type 7 (MVCD-7) 612635 - - - HFE - -
00415 PCT porphyria cutanea tarda (PCT) 176100 AD;AR - - HFE, UROD - -
03576 TFQTL2 transferrin serum level, quantitative trait locus 2 (TFQTL-2) 614193 - - - HFE - -
00416 VP porphyria, variagated (VP) 176200 AD 1 1 HFE, PPOX - -
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