All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00589 ADULT ADULT syndrome (ADULT) 103285 AD 1 1 TP63 - autosomal dominant
00588 AEC;HayWells ankyloblepharon-ectodermal defects-cleft lip/palate (AEC, Hay-Wells syndrome) 106260 AD - - TP63 - autosomal dominant
05538 EEC ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome (EEC) - - 2 2 TP63 - -
00586 EEC3 ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome, type 3 (EEC-3) 604292 AD - - TP63 - autosomal dominant
00590 LMS Limb-mammary syndrome (LMS) 603543 AD - - TP63 - autosomal dominant
05539 OFC8 orofacial cleft, type 8 (OFC-8) 618149 - - - TP63 - -
00591 RHS Rapp-Hodgkin syndrome (RHS) 129400 AD - - TP63 - autosomal dominant
00587 SHFM4 split-hand/foot malformation, type 4 (SHFM-4) 605289 AD 5 3 TP63 - -
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