Hypoaldosteronism

Symptom Information:

Symptom ID: HPO:0004319
Synonyms:
Decreased aldosterone production [HPO:0004319]
Mineralocorticoid insufficiency [HPO:0004319]
Aldosterone deficiency (disorder) [Orphanet:41510]
Hypoaldosteronism [Orphanet:41510]
Hypoaldosteronism [OMIM:Hypoaldosteronism]
Mineralocorticoid insufficiency [OMIM:Mineralocorticoid insufficiency]
Hypoaldosteronism [MedDRA:10020944]
Hyporeninemic hypoaldosteronism [MedDRA:10020944]
Hyperreninemic hypoaldosteronism [MedDRA:10020944]
Hyperreninaemic hypoaldosteronism [MedDRA:10020944]
Hyporeninaemic hypoaldosteronism [MedDRA:10020944]
Mineralocorticoid insufficiency (in 15%) [OMIM:Mineralocorticoid insufficiency (in 15%)]
Quality:
Cross references:
Orphanet:41510 "Hypoaldosteronism" [Orphanet:41510]
OMIM: "Hypoaldosteronism" [OMIM:Hypoaldosteronism]
OMIM: "Mineralocorticoid insufficiency" [OMIM:Mineralocorticoid insufficiency]
OMIM: "Mineralocorticoid insufficiency (in 15%)" [OMIM:Mineralocorticoid insufficiency (in 15%)]
UMLS:C0020595 "Hypoaldosteronism" [HPO:0004319]
UMLS:C0020595 "Hypoaldosteronism" [Orphanet:41510]
Is a (Direct Parents):
Orphanet Abnormality of the adrenal glands
MedDRA Metabolic disorders NEC
HPO         Primary adrenal insufficiency
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the adrenal glands(HPO:0000834)
             Abnormality of adrenal physiology(HPO:0011733)
                Adrenal insufficiency(HPO:0000846)
                   Primary adrenal insufficiency(HPO:0008207)
                      Hypoaldosteronism(HPO:0004319)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Metabolism disorders NEC(MedDRA:10000546)
       Metabolic disorders NEC(MedDRA:10027428)
          Hypoaldosteronism(HPO:0004319)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME (OMIM:231550)
ADRENAL HYPOPLASIA, CONGENITAL (OMIM:300200)
Apparent mineralocorticoid excess (Orphanet:320)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY (OMIM:203400)
CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY (OMIM:610600)
Familial hypoaldosteronism (Orphanet:427)
Liddle syndrome (Orphanet:526)
Triple A syndrome (Orphanet:869)