Autosomal recessive hypohidrotic ectodermal dysplasia (Q87150): Difference between revisions
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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 |
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| 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. |
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CID11:ID_7083042
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dki-india-ID_7083042
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