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