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
01360 - anemia, Heinz body 140700 - - - HBA1, HBA2, HBB - -
02471 - thalassemia, beta, dominant inclusion body type 603902 - - - HBB - -
02472 - anemia, sickle cell (Hb SS disease) 603903 - - - HBB - -
03506 - thalassemia, beta 613985 - - - HBB - -
05164 - anemia - - - - HBB - -
01363 HBFQTL-1 hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1) 141749 - - - HBB, HBG1, HBG2 - -
00309 MLRS malaria, susceptibility to, resistance (MLRS) 611162 - - - CD36, CISH, CR1, FCGR2A, FCGR2B, G6PD, GYPA, GYPB, GYPC, HBB, ICAM1, NOS2, SLC4A1, TIRAP, TNF - -
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