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Diseases
X-Linked Hypohidrotic Ectodermal Dysplasia
x-linked hypohidrotic ectodermal dysplasia
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 2
Basic Information
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Core Information
- Disease Name
- X-Linked Hypohidrotic Ectodermal Dysplasia
- Standard Disease Name
- x-linked hypohidrotic ectodermal dysplasia
- MeSH Tree
- No data
- ICD-10
- Q82.4
Identifiers
- DO ID
- No data
- MeSH ID
- D053358
- OMIM ID
- 305100
- UMLS ID
- C0162359
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A rare genetic disorder characterized by mutations in the gene encoding ectodysplasin A. It results in abnormalities in the morphogenesis of the structures originating from the ectoderm.|MSH2017_2016_08_12:An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.
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