pigmented nodular adrenocortical disease, primary, 1

Preferred Label : pigmented nodular adrenocortical disease, primary, 1;

MeSH note : mutation in PRKAR1A;

MeSH synonym : PPNAD1; adrenocortical nodular dysplasia, primary; pigmented micronodular adrenocortical disease, primary, 1; cushing syndrome, adrenal, due to PPNAD1;

Details

Origin ID

C566469;

UMLS CUI

C1864846;

Automatic exact mappings (from CISMeF team)
- Primary Pigmented Nodular Adrenal Dysplasia [NCIt concept]
Currated CISMeF NLP mapping
- Pigmented nodular adrenocortical disease, primary, 1 [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, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pigmented nodular adrenocortical disease, primary, 1 [OMIM Phenotype]
Validated automatic mappings to NTBT
- Primary pigmented nodular adrenocortical disease [ORDO Disease]

Keyword's position in hierarchy(ies) :

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