Hyperaldosteronism

Symptom Information:

Symptom ID: HPO:0000859
Synonyms:
Elevated plasma aldosterone [HPO:0000859]
Increased aldosterone [HPO:0000859]
Increased aldosterone production [HPO:0000859]
Mineralocorticoid excess [HPO:0000859]
Aldosteronism (disorder) [Orphanet:41480]
Hyperaldosteronism [Orphanet:41480]
Elevated plasma aldosterone [OMIM:Elevated plasma aldosterone]
Hyperaldosteronism [OMIM:Hyperaldosteronism]
Increased aldosterone [OMIM:Increased aldosterone]
Hyperaldosteronism [MedDRA:10020571]
Aldosteronism [MedDRA:10020571]
Aldosteronism NOS [MedDRA:10020571]
Quality:
Cross references:
Orphanet:41480 "Hyperaldosteronism" [Orphanet:41480]
OMIM: "Elevated plasma aldosterone" [OMIM:Elevated plasma aldosterone]
OMIM: "Hyperaldosteronism" [OMIM:Hyperaldosteronism]
OMIM: "Increased aldosterone" [OMIM:Increased aldosterone]
UMLS:C0020428 "Hyperaldosteronism" [HPO:0000859]
UMLS:C0020428 "Hyperaldosteronism" [Orphanet:41480]
Is a (Direct Parents):
MedDRA Endocrine and metabolic secondary hypertension
HPO         Adrenal overactivity
Orphanet Abnormality of the adrenal glands
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 overactivity(HPO:0002717)
                   Hyperaldosteronism(HPO:0000859)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular hypertensive disorders(MedDRA:10057166)
       Endocrine and metabolic secondary hypertension(MedDRA:10052741)
          Hyperaldosteronism(HPO:0000859)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

46,XY disorder of sex development - adrenal insufficiency due to CYP11A1 deficiency (Orphanet:168558)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
BARTTER SYNDROME, TYPE 4A (OMIM:602522)
BARTTER SYNDROME, TYPE 4B (OMIM:613090)
Bartter syndrome (Orphanet:112)
Classic Bartter syndrome (Orphanet:93605)
Congenital chloride diarrhea (Orphanet:53689)
EAST syndrome (Orphanet:199343)
Familial hyperaldosteronism type 1 (Orphanet:403)
Familial hyperaldosteronism type 3 (Orphanet:251274)
Generalized pseudohypoaldosteronism type 1 (Orphanet:171876)
Infantile Bartter syndrome with deafness (Orphanet:89938)
Kearns-Sayre syndrome (Orphanet:480)
Oculocerebrorenal syndrome (Orphanet:534)
Rabson-Mendenhall syndrome (Orphanet:769)
Renal pseudohypoaldosteronism type 1 (Orphanet:171871)