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ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description A form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. It is an autosomal dominant condition characterized by hypotrichosis, abnormal or missing teeth, and hypohidrosis due to the absence of sweat glands.
Mondo Term and Equivalent IDs
MONDO:0013982:  ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant
DOID:0111653: 
UMLS:C3541517: