All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02522 CRS2 craniosynostosis, type 2 (CRS-2) 604757 AD - - MSX2 - -
01491 PFM foramina, parietal (PFM) 168500 AD - - MSX2 - -
01492 PFMCCD foramina, parietal, with cleidocranial dysplasia (PFMCCD) 168550 AD - - MSX2 - -
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