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
05334 CSCF cardiospondylocarpofacial syndrome (CSCF) 157800 AD 1 1 MAP3K7 - -
06697 FMD2 Frontometaphyseal dysplasia 2 617137 AD 1 1 MAP3K7 - -
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