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
00374 NPHP1 nephronophthisis, type 1 256100 AR 77 77 NPHP1, TTC21B - -
03447 NPHP12;JBTS11 nephronophthisis, type 12 (NPHP-12, Joubert syndrome 11 (JBTS-11)) 613820 AD;AR - - TTC21B - -
05635 SRTD dysplasia, short-rib thoracic, with/without polydactyly (SRTD) (Jeune syndrome) - - 22 17 DYNC2H1, IFT43, TTC21B, WDR35, WDR60 - -
03446 SRTD4;ATD4 dysplasia, short-rib thoracic, type 4, with/without polydactyly (SRTD-4, asphyxiating thoracic dystrophy 4 (ATD-4)) 613819 AR - - TTC21B - -
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