All diseases

2 entries on 1 page. Showing entries 1 - 2.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01253 CCD dysplasia, cleidocranial (CCD) 119600 4 2 RUNX2 - -
01437 MDMHB dysplasia, metaphyseal, with maxillary hypoplasia and brachydactyly (MDMHB) 156510 0 0 RUNX2 - -