Familial Hyperaldosteronism

Preferred Label : Familial Hyperaldosteronism;

Alternative definition : NICHD: A heritable form of hyperaldosteronism.;

Origin ID

C127160;

UMLS CUI

C3713420;

Automatic exact mappings (from CISMeF team)
- Familial hyperaldosteronism [ORDO Disease]
- Familial hyperaldosteronism [ICD-11 More detail]
- Familial hyperaldosteronism (disorder) [SNOMED CT concept]
- familial hyperaldosteronism [MeSH concept]
- familial hyperaldosteronism [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hyperaldosteronism [ORDO Disease]
- Familial hyperaldosteronism (disorder) [SNOMED CT concept]
- familial hyperaldosteronism [MeSH Supplementary Concept]
- familial hyperaldosteronism [MeSH concept]
- familial hyperaldosteronism [Disease (Nov.)]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]