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
00373 CED4 dysplasia, cranioectodermal, type 4 (CED-4) 614378 AR - - WDR19 - -
00375 NPHP13 nephronophthisis, type 13 (NPHP-13) 614377 AR - - WDR19 - -
05064 SLSN8 Senior-Loken syndrome, type 8 (SLSN-8) 616307 AR - - WDR19 - -
00376 SRTD5 dysplasia, short-rib thoracic, type 5, with/without polydactyly (SRTD-5) 614376 AR - - WDR19 - -
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