ectodermal dysplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Ectodermal dysplasia is a group of conditions in which there is abnormal development of the skin, hair, nails, teeth, or sweat glands. (Human Phenotype Ontology, HP_0000968)
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6 genes associated with the ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EDARADD EDAR-associated death domain
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
KRT85 keratin 85, type II
MBTPS2 membrane-bound transcription factor peptidase, site 2
ORAI1 ORAI calcium release-activated calcium modulator 1
TP63 tumor protein p63