Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Global developmental delay-osteopenia-ectodermal defect syndrome

This syndrome is characterised by the association of global developmental delay, osteopenia and skin anomalies.

Clinodactyly of the 2nd finger

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PMID (PMCID)