All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05132 ATS Alport syndrome - - 1678 1631 COL4A3, COL4A4, COL4A5 - -
01644 ATS2 Alport syndrome, type 2, autosomal recessive 203780 AR 1009 1011 COL4A4 - -
07068 BFH1 hematuria, benign, familial, type 1 141200 AD - - COL4A4 - -
01361 BFH;TMN hematuria, benign, familial - AD 203 200 COL4A3, COL4A4 - -
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