Ectodermal Dysplasia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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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2 genes/proteins associated with the disease Ectodermal Dysplasia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GJB6 gap junction protein, beta 6, 30kDa 2.88009
ITGB4 integrin, beta 4 2.88009