| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D004476 |
| Similar Terms | |
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2 genes/proteins associated with the disease Ectodermal Dysplasia from the curated CTD Gene-Disease Associations dataset.
