Familial Hyperaldosteronism Type 2

Preferred Label : Familial Hyperaldosteronism Type 2;

Alternative definition : NICHD: Familial hyperaldosteronism unresponsive to glucocorticoid therapy. The molecular basis for this condition has not been fully elucidated.;

Détails

Origin ID

C127162;

UMLS CUI

C1854107;

Automatic exact mappings (from CISMeF team)
- Familial hyperaldosteronism type 2 [ICD-11 More detail]
Currated CISMeF NLP mapping
- Familial hyperaldosteronism type 2 (disorder) [SNOMED CT concept]
- Familial hyperaldosteronism type II [ORDO Disease]
- Hyperaldosteronism, familial, type II [OMIM Phenotype]
- familial hyperaldosteronism type II [Disease (Nov.)]
- hyperaldosteronism, familial, type II [MeSH concept]
- hyperaldosteronism, familial, type II [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hyperaldosteronism type 2 (disorder) [SNOMED CT concept]
- Hyperaldosteronism, familial, type II [OMIM Phenotype]
- hyperaldosteronism, familial, type II [MeSH Supplementary Concept]
- hyperaldosteronism, familial, type II [MeSH concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
related_to_genetic_biomarker
- CLCN2 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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