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
06666 JBTS31 Joubert syndrome 31 617761 AR - - CEP120 - -
04404 SRTD13 dysplasia, short-rib thoracic, type 13 with/without polydactyly (SRTD-13) 616300 AR - - CEP120 - -
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