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
04510 RP71 retinitis pigmentosa, type 71 (RP71) 616394 AR - - IFT172 - -
04035 SRTD10 dysplasia, thoracic, short-rib, type 10 with/without polydactyly (SRTD-10) 615630 AR 14 14 IFT172 - -
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