|
DOID:0060438 - Cole-Carpenter syndrome
Disease Ontology Definition:An osteogenesis imperfecta characterized by craniosynostosis, communicating hydrocephalus, ocular proptosis, marked postnatal growth failure, and distinctive facial appearance.
Synonyms:
Xenbase Genes : p4hb, sec24d
MONDO:0016085 - Cole-Carpenter syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
osteogenesis imperfecta (is_a)