Glucocorticoid-Remediable aldosteronism

Preferred Label : Glucocorticoid-Remediable aldosteronism;

MeSH note : PROM syndrome is the result of an anti-Lepore-type fusion of the CYP11B2 and CYP11B1 genes;

MeSH synonym : aldosteronism, sensitive to dexamethasone; hyperaldosteronism, familial, type I; ACTH-Dependent hyperaldosteronism syndrome; Glucocorticoid-Suppressible hyperaldosteronism;

Détails

Origin ID

C563177;

UMLS CUI

C3838731;

Currated CISMeF NLP mapping
- Familial Hyperaldosteronism Type 1 [NCIt concept]
- Familial hyperaldosteronism type 1 [ICD-11 More detail]
- Familial hyperaldosteronism type 1 (disorder) [SNOMED CT concept]
- Familial hyperaldosteronism type I [ORDO Disease]
- Glucocorticoid Suppressible Hyperaldosteronism [NCIt concept]
- Glucocorticoid-remediable aldosteronism [ICD-9 code]
- Glucocorticoid-suppressible hyperaldosteronism (disorder) [SNOMED CT concept]
- Hyperaldosteronism, familial, type I [OMIM Phenotype]
- familial hyperaldosteronism type I [Disease (Nov.)]
- glucocorticoid-remediable aldosteronism [DO Concept]
DO Cross reference
- glucocorticoid-remediable aldosteronism [DO Concept]
MeSH term(s) associated for indexing
- hyperaldosteronism [MeSH Descriptor]
Record concept(s)
- Glucocorticoid-Remediable aldosteronism [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Hyperaldosteronism Type 1 [NCIt concept]
- Familial hyperaldosteronism type 1 (disorder) [SNOMED CT concept]
- Familial hyperaldosteronism type I [ORDO Disease]
- Glucocorticoid Suppressible Hyperaldosteronism [NCIt concept]
- Glucocorticoid-remediable aldosteronism [ICD-9 code]
- Glucocorticoid-suppressible hyperaldosteronism (disorder) [SNOMED CT concept]
- Hyperaldosteronism, familial, type I [OMIM Phenotype]
- familial hyperaldosteronism type I [Disease (Nov.)]
- glucocorticoid-remediable aldosteronism [DO Concept]

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