|
DOID:0080033 - craniometaphyseal dysplasia
Disease Ontology Definition:An osteosclerosis that is characterized by hyperostosis and sclerosis of the craniofacial bones associated with abnormal modeling of the metaphyses.
Synonyms:
Xenbase Genes
:
gja1,
wdr19,
ankh,
ift43
| MONDO:0015465 - craniometaphyseal dysplasia |
| MIM:123000 - CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CMDD |
| MIM:614099 - CRANIOECTODERMAL DYSPLASIA 3; CED3 |
| MIM:614378 - CRANIOECTODERMAL DYSPLASIA 4; CED4 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
osteosclerosis (is_a)