|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A monogenic disease that is characterized by malformation of ectodermal (skin, hair, teeth and sweat glands) structures including hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth). (Human Disease Ontology, DOID_14793)|
|Downloads & Tools|
1 genes associated with the hypohidrotic ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|EDARADD||EDAR-associated death domain|