Hyperkalemia
Symptom Information:
Symptom ID: | HPO:0002153 | ||||||||||||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of ion homeostasis(HPO:0003111) Abnormality of cation homeostasis(HPO:0010929) Abnormality of monovalent inorganic cation homeostasis(HPO:0010930) Abnormality of potassium homeostasis(HPO:0011042) Hyperkalemia(HPO:0002153) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Electrolyte and fluid balance conditions(MedDRA:10014412) Potassium imbalance(MedDRA:10036451) Hyperkalemia(HPO:0002153) |
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Database Frequency: | 25 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY | (OMIM:203400) |
CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY | (OMIM:610600) |
Cytomegalic congenital adrenal hypoplasia | (Orphanet:95702) |
Familial hypoaldosteronism | (Orphanet:427) |
Generalized pseudohypoaldosteronism type 1 | (Orphanet:171876) |
Genetic recurrent myoglobinuria | (Orphanet:99845) |
HYPERCHLORHIDROSIS, ISOLATED | (OMIM:143860) |
HYPOADRENOCORTICISM, FAMILIAL | (OMIM:240200) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Kasabach-Merritt syndrome | (Orphanet:2330) |
King-Denborough syndrome | (Orphanet:99741) |
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2 | (OMIM:154275) |
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3 | (OMIM:154276) |
MELAS | (Orphanet:550) |
Malignant hyperthermia | (Orphanet:423) |
Myotonia fluctuans | (Orphanet:99734) |
Nephronophthisis 2 | (OMIM:602088) |
Potassium-aggravated myotonia | (Orphanet:612) |
Pseudohypoaldosteronism type 2 | (Orphanet:757) |
Pseudohypoaldosteronism type 2A | (Orphanet:88938) |
Pseudohypoaldosteronism type 2B | (Orphanet:88939) |
Pseudohypoaldosteronism type 2C | (Orphanet:88940) |
Pseudohypoaldosteronism type 2D | (Orphanet:300525) |
Pseudohypoaldosteronism type 2E | (Orphanet:300530) |
Renal pseudohypoaldosteronism type 1 | (Orphanet:171871) |