Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema

Preferred Label : Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema;

Obsolete resource : true;

Moved to : 300291;

Symbol : OLEDAID;

CISMeF acronym : OLEDAID;

Type : Phenotype, molecular basis known;

Prefixed ID : 300301;

Details

Origin ID

300301;

UMLS CUI

C1845919;

CISMeF manual mappings
- Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome [ORDO Disease]
- OL-EDA-ID syndrome [ICD-11 More detail]
- ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema [MeSH Supplementary Concept]
- ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema [MeSH concept]
ORDO concept(s)
- Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome [ORDO Disease]
- ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema [MeSH Supplementary Concept]
- ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema [MeSH concept]

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