All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02471 - thalassemia, beta, dominant inclusion body type 603902 - 1 1 HBB - -
05164 - anemia - - 0 0 HBB, VPS4A - -
06122 - Methmoglobinemia, beta type 617971 - 0 0 HBB - -
01360 anemia, Heinz anemia, Heinz body 140700 AD 0 0 HBA1, HBA2, HBB - -
02472 anemia, sickle cell anemia, sickle cell (HbS disease) 603903 AR 11 10 HBB - -
06123 ECYT6 Erythrocytosis 6 617980 - 0 0 HBB - -
01363 HBFQTL1 hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1) 141749 AD 1 2 HBB, HBG1, HBG2 - -
00309 MLRS malaria, susceptibility to 611162 - 3 1 CD36, CISH, CR1, DARC, FCGR2A, FCGR2B, G6PD, GYPA, GYPB, GYPC, HBB, ICAM1, NOS2, SLC4A1, TIRAP, TNF - -
05669 thal thalassemia - - 1982 1982 HBA1, HBA2, HBB, HBD, HBG1, HBG2, SUPT5H - -
03506 thalbeta thalassemia, beta (thalassemia, Hispanic gamma-delta-beta) 613985 - 437 437 HBB - -
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