All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05875 SRTD19 dysplasia, thoracic, short-rib, type 19 with/without polydactyly (SRTD19) 617895 AR - - IFT81 - -
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