All diseases

4 entries on 1 page. Showing entries 1 - 4.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01169 ASAD syndrome, Alport, autosomal dominant (ASAD) 104200 40 45 COL4A3 - -
01644 ASAR syndrome, Alport, autosomal dominant (ASAR) 203780 1003 1005 COL4A3, COL4A4 - -
01361 BFH;TBMN hematuria, benign, familial (BFH, thin basement membrane nephropathy (TBMN)) 141200 190 190 COL4A3 - -
04425 MRD-34 mental retardation, autosomal dominant, type 34 (MRD-34) 616351 0 0 COL4A3BP - -