Disease-gene associations mined from literature

Human genes for hypohidrotic ectodermal dysplasia

Hypohidrotic ectodermal dysplasia [DOID:14793]

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).

Synonyms:  hypohidrotic ectodermal dysplasia,  DOID:14793,  Christ-Siemens-Touraine Syndrome,  Ectodermal Dysplasia 1, Anhydrotic,  Hypohidrotic X-linked ectodermal dysplasia (disorder) ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6