All diseases

2 entries on 1 page. Showing entries 1 - 2.
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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 - - 2 4 COL4A5 - -
02210 ATS1 Alport syndrome, X-linked recessive (ATS1) 301050 XLD 103 102 COL4A5 - -
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