All diseases

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00297 GCPS cephalopolysyndactyly, Greig syndrome (GCPS) 175700 AD 55 55 GLI3 - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
00300 PAPA1;PAPB polydactyly, postaxial, type A1 (PAPA-1, type B included (PAPB)) 174200 AD 1 1 GLI3 - autosomal dominant
00299 PHS Pallister-Hall syndrome (PHS) 146510 AD 26 23 GLI3 - -
00301 PPD4 polydactyly, preaxial, type IV (PPD4) 174700 AD 1 1 GLI3 - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.