All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01076 - Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis - - 3 5 COL4A5 - -
05132 ATS Alport syndrome - - 1678 1631 COL4A3, COL4A4, COL4A5 - -
02210 ATS1 Alport syndrome, type 1, X-linked 301050 XLD 141 140 COL4A5 - -
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