Increased circulating renin level
Symptom Information:
Symptom ID: | HPO:0000848 | ||||||||
Synonyms: |
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Quality: | |||||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |