Hypoaldosteronism
Symptom Information:
Symptom ID: | HPO:0004319 | ||||||||||||
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 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) |
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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) |