Increased circulating renin level

Symptom Information:

Symptom ID: HPO:0000848
Synonyms:
Elevated plasma renin [HPO:0000848]
Hyperreninemia [HPO:0000848]
Increased plasma renin [HPO:0000848]
Increased serum renin [HPO:0000848]
Elevated plasma renin [OMIM:Elevated plasma renin]
Increased plasma renin [OMIM:Increased plasma renin]
Increased serum renin [OMIM:Increased serum renin]
Hyperreninemia (rare) [OMIM:Hyperreninemia (rare)]
Quality:
Cross references:
OMIM: "Elevated plasma renin" [OMIM:Elevated plasma renin]
OMIM: "Increased plasma renin" [OMIM:Increased plasma renin]
OMIM: "Increased serum renin" [OMIM:Increased serum renin]
OMIM: "Hyperreninemia (rare)" [OMIM:Hyperreninemia (rare)]
Is a (Direct Parents):
HPO         Abnormality of renin-angiotensin system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of renin-angiotensin system(HPO:0000847)
             Increased circulating renin level(HPO:0000848)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
Bartter syndrome (Orphanet:112)
Bartter syndrome with hypocalcemia (Orphanet:263417)
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY (OMIM:203400)
CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY (OMIM:610600)
Classic Bartter syndrome (Orphanet:93605)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Cytomegalic congenital adrenal hypoplasia (Orphanet:95702)
EAST syndrome (Orphanet:199343)
Familial hypoaldosteronism (Orphanet:427)
Gitelman syndrome (Orphanet:358)
HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY (OMIM:241150)
Renal pseudohypoaldosteronism type 1 (Orphanet:171871)