Familial Hyperaldosteronism Type 1

Preferred Label : Familial Hyperaldosteronism Type 1;

NCIt related terms : Glucocorticoid Suppressible Hypertension; Glucocorticoid Remediable Aldosteronism; CYP11B1/CYP11B2 Chimerism;

Alternative definition : NICHD: Familial hyperaldosteronism caused by a chimeric gene containing regions of CYP11B1 and CYP11B2. This condition is responsive to exogenous glucocorticoids.;

NCI Metathesaurus CUI : CL508854;

Details

Origin ID

C127161;

UMLS CUI

C3838731;

Currated CISMeF NLP mapping
- Familial hyperaldosteronism type 1 [ICD-11 More detail]
- Familial hyperaldosteronism type 1 (disorder) [SNOMED CT concept]
- Familial hyperaldosteronism type I [ORDO Disease]
- Glucocorticoid-Remediable aldosteronism [MeSH Supplementary Concept]
- Glucocorticoid-Remediable aldosteronism [MeSH concept]
- Hyperaldosteronism, familial, type I [OMIM Phenotype]
- glucocorticoid-remediable aldosteronism [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hyperaldosteronism type 1 (disorder) [SNOMED CT concept]
- Glucocorticoid-Remediable aldosteronism [MeSH Supplementary Concept]
- Glucocorticoid-remediable aldosteronism [ICD-9 code]
- Glucocorticoid-suppressible hyperaldosteronism (disorder) [SNOMED CT concept]
- Hyperaldosteronism, familial, type I [OMIM Phenotype]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
related_to_genetic_biomarker
- CYP11B1 Gene [NCIt concept]
- CYP11B2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients