hypohidrotic ectodermal dysplasia Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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)
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Genes

3 genes involed in the disease hypohidrotic ectodermal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
EDA ectodysplasin A
EDAR ectodysplasin A receptor
EDARADD EDAR-associated death domain