Autosomal recessive hypohidrotic ectodermal dysplasia (Q87150): Difference between revisions

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Latest revision as of 12:43, 15 August 2026

Ectodermal hypohidrotic or anhidrotic dysplasia is an ectodermal dysplasia syndrome characterised by decreased or absent sudation, intolerance to heat, dry, sparse hair, very fine skin, total or partial lack of teeth, characteristic facial dysmorphism, all of which are often associated with ocular, digestive, or pulmonary disorders.

Language	Label	Description	Also known as
default for all languages	ID_7083042
English	Autosomal recessive hypohidrotic ectodermal dysplasia	Ectodermal hypohidrotic or anhidrotic dysplasia is an ectodermal dysplasia syndrome characterised by decreased or absent sudation, intolerance to heat, dry, sparse hair, very fine skin, total or partial lack of teeth, characteristic facial dysmorphism, all of which are often associated with ocular, digestive, or pulmonary disorders.