Skip to
  1. Homepage
  2. Rare diseases
  3. Search
Simple search

Simple search

*
(*) mandatory field





 

Other search option(s)

Autosomal dominant hypohidrotic ectodermal dysplasia

ORPHA1810
Synonym(s) AD-HED
Autosomal dominant anhidrotic ectodermal dysplasia
Prevalence <1 / 1 000 000
Inheritance Autosomal dominant
Age of onset Infancy
Neonatal
ICD-10
  • Q82.4
OMIM
UMLS
  • C0265331
MeSH -
MedDRA -

Summary

This disease is described under Hypohidrotic ectodermal dysplasia


(*) Required fields.

Attention: Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.


Captcha image

Detailed information

Article for general public
  • EN (2011)
Clinical genetics review
  • EN (2014)
Get Acrobat Reader
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.