All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02221 CPDX-1 chondrodysplasia punctata, type 1, X-linked recessive (CPDX-1) 302950 56 56 ARSE - -