|
DOID:2121 - ectodermal dysplasia
Disease Ontology Definition:A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.
Synonyms: Congenital ectodermal defect, Congenital ectodermal defect (disorder), Congenital ectodermal dysplasia, Ectodermal dysplasia (disorder),
Xenbase Genes
:
wnt10a,
hoxc13,
tp63,
kremen1,
cdh3,
nfkbia,
smarcad1,
gja1,
ctsc,
edar,
ikbkg,
edaradd,
kdf1,
setbp1,
kctd1,
| MONDO:0019287 - ectodermal dysplasia syndrome |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)