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
00278 IBGC4 calcification, basal ganglia, idiopathic, type 4 (IBGC-4) 615007 AD 1 1 PDGFRB - -
01785 IMF1 myofibromatosis, infantile, type 1 (IMF-1) 228550 AD 7 7 PDGFRB - -
05222 KOGS Kosaki overgrowth syndrome (KOGS) 616592 AD 4 4 PDGFRB - -
01306 MPE Myeloproliferative disorder, chronic, with eosinophilia 131440 AD - - PDGFRB - -
04329 PENTT aging, premature, syndrome, Penttinen type (PENTT) 601812 AD 4 4 PDGFRB - -
Legend   How to query  


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