Pigmented nodular adrenocortical disease, primary, 3

Preferred Label : Pigmented nodular adrenocortical disease, primary, 3;

Symbol : PPNAD3;

CISMeF acronym : PPNAD3;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Cushing syndrome, adrenal, due to ppnad3;

Prefixed ID : #614190;

Details

Origin ID

614190;

UMLS CUI

C3280094;

DO Cross reference
- primary pigmented nodular adrenocortical disease [DO Concept]
Genes related to phenotype
- Phosphodiesterase 8b [OMIM gene]
HPO term(s)
- Adrenal hyperplasia [HPO term]
- Autosomal dominant inheritance [HPO term]
- Increased circulating cortisol level [HPO term]
ORDO concept(s)
- Primary pigmented nodular adrenocortical disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to NTBT
- Primary pigmented nodular adrenocortical disease [ORDO Disease]
- primary pigmented nodular adrenocortical disease [DO Concept]

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