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
06314 PEERB Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 618331 AR - - TRAPPC2L - -
02266 SEDT Spondyloepiphyseal dysplasia tarda 313400 XLR - - TRAPPC2 - -
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