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
00003 abnormal hemoglobin abnormal hemoglobin - - 12 - HBA1, HBA2, HBB, HBD, HBE1, HBG1, HBG2 - -
00004 HPFH Hereditary persistence of fetal hemoglobin - - 5 - HBB, HBD, HBE1, HBG1, HBG2 - -
00019 WD wilson disease 277900 AR - - ABCC9, ACADM, ACADS, ACADVL, ACAT1, ACTC1, ACTN2, AKAP9, ANK2, APC, ATP7B, AXIN2, BARD1, BCL11A, BRCA1, BRCA2, BRIP1, CACNA1C, CAV3, CDC73, 107 more brain liver dysfunction, neurological features (like tremor, parkinsonism, dystornia, etc.), Kayser-Fleischer rings, chondrocalcinosis and osteoarthritis...
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