ectodermal dysplasia 3, anhidrotic

Preferred Label : ectodermal dysplasia 3, anhidrotic;

MeSH definition : An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.;

MeSH synonym : ectodermal dysplasia, hypohidrotic, autosomal dominant;

Details

Origin ID

D053359;

UMLS CUI

C1720965;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- hypohidrotic ectodermal dysplasia [DO Concept]
Currated CISMeF NLP mapping
- Autosomal dominant hypohidrotic ectodermal dysplasia [ICD-11 More detail]
- Autosomal dominant hypohidrotic ectodermal dysplasia [ORDO Disease]
- Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) [SNOMED CT concept]
- hypohidrotic ectodermal dysplasia autosomal dominant [Disease (Nov.)]
Record concept(s)
- ectodermal dysplasia 3, anhidrotic [MeSH concept]
See also
- edar receptor [MeSH Descriptor]
See also inter- (CISMeF)
- Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant [OMIM Phenotype]
- Ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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