pigmented nodular adrenocortical disease, primary, 2

Preferred Label : pigmented nodular adrenocortical disease, primary, 2;

MeSH note : mutation in PDE11A;

MeSH synonym : PPNAD2; cushing syndrome, adrenal, due to PPNAD2; pigmented micronodular adrenocortical disease, primary, 2;

Details

Origin ID

C566472;

UMLS CUI

C1864851;

Currated CISMeF NLP mapping
- Pigmented nodular adrenocortical disease, primary, 2 [OMIM Phenotype]
DO Cross reference
- primary pigmented nodular adrenocortical disease [DO Concept]
MeSH term(s) associated for indexing
- adrenal cortex diseases [MeSH Descriptor]
Record concept(s)
- pigmented nodular adrenocortical disease, primary, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pigmented nodular adrenocortical disease, primary, 2 [OMIM Phenotype]
Validated automatic mappings to NTBT
- primary pigmented nodular adrenocortical disease [DO Concept]

Keyword's position in hierarchy(ies) :

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