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
05650 AI amelogenesis imperfecta (AI) - - 75 73 AMBN, AMELX, MMP20 - -
03148 AI2A2 amelogenesis imperfecta, hypomaturation type, IIA2 (AI2A2) 612529 AR - - MMP20 - -
05733 HTX7 heterotaxy, visceral, autosomal, type 7 (HTX7) - AR - - MMP21 - -
06071 HTX7 Heterotaxy, visceral, 7, autosomal 616749 AR - - MMP21 - -
01990 MONA osteolysis, multicentric, nodulosis, and arthropathy 259600 AR 2 1 MMP2 - -
Legend   How to query  


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