Hyperaldosteronism
Symptom Information:
Symptom ID: | HPO:0000859 | ||||||||||||
Synonyms: |
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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 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) |
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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) |