All diseases

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05132 ATS Alport syndrome - - 1678 1631 COL4A3, COL4A4, COL4A5 - -
01169 ATS3A Alport syndrome, type 3A, autosomal dominant 104200 AD 49 53 COL4A3 - -
07070 ATS3B Alport syndrome, type 3B, autosomal recessive 620536 AR - - COL4A3 - -
07069 BFH2 hematuria, benign, familial, type 2 620320 AD - - COL4A3 - -
01361 BFH;TMN hematuria, benign, familial - AD 203 200 COL4A3, COL4A4 - -
04425 MRD34 mental retardation, autosomal dominant, type 34 (MRD-34) 616351 AD - - COL4A3BP - -
Legend   How to query  


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