adrenocortical hypofunction, chronic primary congenital

Preferred Label : adrenocortical hypofunction, chronic primary congenital;

MeSH synonym : addison disease, congenital;

Is substance : O;

Details

Origin ID

C562711;

UMLS CUI

C0271740;

Currated CISMeF NLP mapping
- Adrenocortical hypofunction, chronic primary congenital [OMIM Phenotype]
- Congenital primary adrenocortical hypofunction (disorder) [SNOMED CT concept]
- congenital primary adrenocortical hypofunction [SNOMED Notion]
MeSH term(s) associated for indexing
- adrenal insufficiency [MeSH Descriptor]
- genetic diseases, inborn [MeSH Descriptor]
Record concept(s)
- adrenocortical hypofunction, chronic primary congenital [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Adrenocortical hypofunction, chronic primary congenital [OMIM Phenotype]
- Congenital primary adrenocortical hypofunction (disorder) [SNOMED CT concept]
- congenital primary adrenocortical hypofunction [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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