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
05725 RP80 retinitis pigmentosa, type 80 (RP80) 617781 AR - - IFT140 - -
00715 SRTD9;MZSDS dysplasia, short-rib thoracic, type 9, with/without polydactyly (SRTD9);syndrome, Mainzer-Saldino (MZSDS) 266920 AR 2 2 IFT140 - -
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