Pseudohypoaldosteronism Type 2

Preferred Label : Pseudohypoaldosteronism Type 2;

NCIt related terms : Gordon Syndrome;

Alternative definition : NICHD: A hereditary renal tubular defect characterized by hypertension and hyperkalemic metabolic acidosis in the presence of suppressed plasma renin levels and relatively low aldosterone levels.;

Details

Origin ID

C123252;

UMLS CUI

C1449844;

Automatic exact mappings (from CISMeF team)
- Arthrogryposis, distal, type 3 [OMIM Phenotype]
- Gordon syndrome [MeSH concept]
- Gordon syndrome [ORDO Disease]
- Gordon's syndrome (disorder) [Inactive SNOMED CT concept]
- distal arthrogryposis type 3 [DO Concept]
- gordon syndrome [MeSH Supplementary Concept]
- pseudohypoaldosteronism [MeSH Descriptor]
Currated CISMeF NLP mapping
- Pseudohypoaldosteronism type 2 [ORDO Disease]
- Pseudohypoaldosteronism type 2 [PASCAL descriptor]
- Pseudohypoaldosteronism type 2 [ICD-11 More detail]
- Pseudohypoaldosteronism, type 2 (disorder) [SNOMED CT concept]
- pseudohypoaldosteronism type 2 [Disease (Nov.)]
- pseudohypoaldosteronism, type 2 [SNOMED Notion]
- pseudohypoaldosteronism, type II [MeSH concept]
False automatic mappings
- Gordon syndrome [MedDRA LLT]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pseudohypoaldosteronism type 2 [ORDO Disease]
- Pseudohypoaldosteronism type 2 [PASCAL descriptor]
- Pseudohypoaldosteronism, type 2 (disorder) [SNOMED CT concept]
- pseudohypoaldosteronism type 2 [Disease (Nov.)]
- pseudohypoaldosteronism, type 2 [SNOMED Notion]
- pseudohypoaldosteronism, type II [MeSH concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Nephrology Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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