pseudohypoaldosteronism

Preferred Label : pseudohypoaldosteronism;

MeSH definition : A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION.;

MeSH synonym : pseudohypoaldosteronisms;

CISMeF synonym : type 1s, pseudohypoaldosteronism; type 2, pseudohypoaldosteronism; type 2s, pseudohypoaldosteronism; type I pseudohypoaldosteronisms; I, pseudohypoaldosteronism type; is, pseudohypoaldosteronism type;

MeSH hyponym : hyperpotassemia and hypertension, familial; pseudohypoaldosteronism, type II; pseudohypoaldosteronism, type I; pseudohypoaldosteronism, type I, autosomal recessive; pseudohypoaldosteronism, type I, autosomal dominant; Pseudohypoaldosteronisms, Type I; Type I Pseudohypoaldosteronism; Pseudohypoaldosteronism Type 1; Pseudohypoaldosteronism Type 1s; Type 1, Pseudohypoaldosteronism; Pseudohypoaldosteronism Type I; Pseudohypoaldosteronism Type Is; Type I, Pseudohypoaldosteronism; Type Is, Pseudohypoaldosteronism; Pseudohypoaldosteronisms, Type II; Type II Pseudohypoaldosteronism; Type II Pseudohypoaldosteronisms; Gordon Hyperkalemia-Hypertension Syndrome; Gordon Hyperkalemia Hypertension Syndrome; Hyperkalemia-Hypertension Syndrome, Gordon; Syndrome, Gordon Hyperkalemia-Hypertension; Pseudohypoaldosteronism Type 2; Pseudohypoaldosteronism Type 2s; Pseudohypoaldosteronism Type II; Pseudohypoaldosteronism Type IIs; Type II, Pseudohypoaldosteronism; Type IIs, Pseudohypoaldosteronism; Pseudohypoaldosteronism Type 1, Autosomal Recessive; Familial Hyperpotassemia and Hypertension; Familial Hypertensive Hyperkalemia; Hypertensive Hyperkalemia, Familial; Familial Hypertensive Hyperkalemias; Hyperkalemia, Familial Hypertensive; Hyperkalemias, Familial Hypertensive; Hypertensive Hyperkalemias, Familial; Pseudohypoaldosteronism Type 1, Autosomal Dominant;

Wikipedia link : https://en.wikipedia.org/wiki/Pseudohypoaldosteronism;

Details

Origin ID

D011546;

UMLS CUI

C0033805;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Aldosterone deficiency (disorder) [SNOMED CT concept]
- Arthrogryposis, distal, type 3 [OMIM Phenotype]
- Generalized pseudohypoaldosteronism type 1 [ORDO Disease]
- Gordon syndrome [ORDO Disease]
- Gordon syndrome [MedDRA LLT]
- Gordon's syndrome (disorder) [Inactive SNOMED CT concept]
- Hyperkalemic Mineralocorticoid Resistance [NCIt concept]
- Hypoaldosteronism [HPO term]
- Hypoaldosteronism [MedDRA Preferred Term]
- Hyponatremic Mineralocorticoid Resistance due to Mineralocorticoid Receptor Defect [NCIt concept]
- Other and unspecified adrenocortical insufficiency [ICD-10 Sub-category (who)]
- Pseudohypoaldosteronism Type 2 [NCIt concept]
- Pseudohypoaldosteronism type 1 [PASCAL descriptor]
- Pseudohypoaldosteronism type 1 [ICD-11 Sub-sub category]
- Pseudohypoaldosteronism type 1 [ORDO Disease]
- Pseudohypoaldosteronism type 2 [PASCAL descriptor]
- Pseudohypoaldosteronism type 2 [ICD-11 More detail]
- Pseudohypoaldosteronism type 2 [ORDO Disease]
- Pseudohypoaldosteronism type 2A (disorder) [SNOMED CT concept]
- Pseudohypoaldosteronism type ii [HPO term]
- Pseudohypoaldosteronism, type 1 (disorder) [SNOMED CT concept]
- Pseudohypoaldosteronism, type 2 (disorder) [SNOMED CT concept]
- Pseudohypoaldosteronism, type I, autosomal dominant [OMIM Phenotype]
- Pseudohypoaldosteronism, type II [OMIM phenotypic series]
- Pseudohypoaldosteronism, type ib1, autosomal recessive [OMIM Phenotype]
- Renal pseudohypoaldosteronism type 1 [ORDO Disease]
- aldosterone deficiency, nos [SNOMED Notion]
- pseudohypoaldosteronism, type 1 [SNOMED Notion]
- pseudohypoaldosteronism, type 2 [SNOMED Notion]
Currated CISMeF NLP mapping
- Pseudohypoaldosteronism [PASCAL descriptor]
- Pseudohypoaldosteronism [ORDO Disease]
- Pseudohypoaldosteronism [HPO term]
- Pseudohypoaldosteronism [MedDRA Preferred Term]
- Pseudohypoaldosteronism [NCIt concept]
- Pseudohypoaldosteronism (disorder) [SNOMED CT concept]
- pseudohypoaldosteronism [DO Concept]
- pseudohypoaldosteronism [Disease (Nov.)]
- pseudohypoaldosteronism, nos [SNOMED Notion]
DO Cross reference
- autosomal dominant pseudohypoaldosteronism type 1 [DO Concept]
- autosomal recessive pseudohypoaldosteronism type 1 [DO Concept]
- pseudohypoaldosteronism [DO Concept]
HPO term
- Pseudohypoaldosteronism [HPO term]
Manual BTNT mappings - CISMeF
- Pseudohypoaldosteronism type 2A [ORDO Disease]
- Pseudohypoaldosteronism type 2B [ORDO Disease]
- Pseudohypoaldosteronism type 2C [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare cause of hypertension [ORDO Disease]
- Rare genetic cause of hypertension [ORDO Disease]
ORDO relation(s)
- Pseudohypoaldosteronism type 1 [ORDO Disease]
Record concept(s)
- hyperpotassemia and hypertension, familial [MeSH concept]
- pseudohypoaldosteronism [MeSH concept]
- pseudohypoaldosteronism, type I [MeSH concept]
- pseudohypoaldosteronism, type I, autosomal dominant [MeSH concept]
- pseudohypoaldosteronism, type I, autosomal recessive [MeSH concept]
- pseudohypoaldosteronism, type II [MeSH concept]
Related MeSH Supplementary Concept(s)
- pseudohypoaldosteronism, type IIa [MeSH Supplementary Concept]
- pseudohypoaldosteronism, type IIb [MeSH Supplementary Concept]
- pseudohypoaldosteronism, type IIc [MeSH Supplementary Concept]
- tunglang savage bellman syndrome [MeSH Supplementary Concept]
See also
- aldosterone [MeSH Descriptor]
- epithelial sodium channels [MeSH Descriptor]
- receptors, mineralocorticoid [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pseudohypoaldosteronism [HPO term]
- Pseudohypoaldosteronism [ORDO Disease]
- Pseudohypoaldosteronism [PASCAL descriptor]
- Pseudohypoaldosteronism [MedDRA Preferred Term]
- Pseudohypoaldosteronism [NCIt concept]
- Pseudohypoaldosteronism (disorder) [SNOMED CT concept]
- pseudohypoaldosteronism [DO Concept]
- pseudohypoaldosteronism [Disease (Nov.)]
- pseudohypoaldosteronism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Pseudohypoaldosteronism Type 1 [NCIt concept]
- Pseudohypoaldosteronism, type iia [OMIM Phenotype]
- autosomal dominant pseudohypoaldosteronism type 1 [DO Concept]
- autosomal recessive pseudohypoaldosteronism type 1 [DO Concept]
- pseudohypoaldosteronism type 1 [Disease (Nov.)]
- pseudohypoaldosteronism type 2 [Disease (Nov.)]

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