Cole-Carpenter syndrome

Summary
Definition
An osteogenesis imperfecta characterized by craniosynostosis, communicating hydrocephalus, ocular proptosis, marked postnatal growth failure, and distinctive facial appearance.
Super Class
osteogenesis imperfecta
Disease Ontology
DOID:0060438
Mondo Disease Ontology
MeSH
NCI Thesaurus
ORDO
OMIM
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
5034 P4HB prolyl 4-hydroxylase subunit beta
9871 SEC24D SEC24 homolog D, COPII coat complex component
Displaying 1 entry
Gene ID Gene Symbol Description Source
69608 Sec24d SEC24 homolog D, COPII coat complex component
Displaying 1 entry
Gene ID Gene Symbol Description Source
180724 pdi-2 Protein disulfide-isomerase 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
850314 PDI1 protein disulfide isomerase PDI1
852130 EUG1 protein disulfide isomerase EUG1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024