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
05635 SRTD dysplasia, short-rib thoracic, with/without polydactyly (SRTD) (Jeune syndrome) - - 22 17 DYNC2H1, IFT43, TTC21B, WDR35, WDR60 - -
03972 SRTD8;SRPS6 dysplasia, thoracic, short-rib, type 8 with/without polydactyly (SRTD8, short rib polydactyly syndrome 6 (SRPS6)) 615503 AR - - WDR60 - -
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