All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

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 - -
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