All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03208 AHUS6 hemolyticuremic syndrome, atypical, type 6 (AHUS6) 612926 AD - - THBD - -
05669 thal thalassemia - - 1982 1982 HBA1, HBA2, HBB, HBD, HBG1, HBG2, SUPT5H - -
03662 THPH12 Thrombophilia due to thrombomodulin defect 614486 - - - THBD - -
01405 TOC tylosis, with esophageal cancer (TOC, Howel-Evans syndrome) 148500 AD - - RHBDF2 - -
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