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
01670 - asthma, nasal polyps, and aspirin intolerance 208550 AR - - PTGER2, TBX21 - -
02220 ABERS Abruzzo Erickson syndrome (ABERS) 302905 XL - - TBX22 - -
04204 ASD septal defect, atrial (ASD) - - 92 93 TBX20 - -
03022 ASD4 septal defect, atrial, type 4 (ASD4) 611363 - 1 1 TBX20 - -
02224 CPX cleft palate, with/without ankyloglossia, X-linked (CPX) 303400 XL 39 38 TBX22 - -
05086 HL hearing loss (HL) - - 1334 1221 ATOH1, C10orf90, FAM179A, GRAP, MPZL2, PDZD7, PKHD1L1, TBX2, USP48 - -
06365 VETD Vertebral anomalies and variable endocrine and T-cell dysfunction 618223 AD - - TBX2 - -
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