Hyperkalemia

Symptom Information:

Symptom ID: HPO:0002153
Synonyms:
Hyperkalemia (disorder) [Orphanet:49160]
Potassium overload (disorder) [Orphanet:49160]
HYPERKALAEMIA [HPO:0002153]
Hyperkalemia [Orphanet:49160]
Hyperkalemia [OMIM:Hyperkalemia]
Hyperkalaemia [Orphanet:49160]
Hyperkalaemia [MedDRA:10020646]
Hyperkalemia [MedDRA:10020646]
Hyperpotassaemia [MedDRA:10020646]
Hyperpotassemia [MedDRA:10020646]
Hyperkalemia (5.8 +/- 0.8 mM) [OMIM:Hyperkalemia (5.8 +/- 0.8 mM)]
Hyperkalemia (6.4 +/- 0.7 mM) [OMIM:Hyperkalemia (6.4 +/- 0.7 mM)]
Hyperkalemia (7.5 +/- 0.9 mM) [OMIM:Hyperkalemia (7.5 +/- 0.9 mM)]
Hyperkalemia (>6.2 mM in both dominant and recessive) [OMIM:Hyperkalemia (>6.2 mM in both dominant and recessive)]
Quality:
Cross references:
Orphanet:49160 "Hyperkalemia" [Orphanet:49160]
OMIM: "Hyperkalemia" [OMIM:Hyperkalemia]
OMIM: "Hyperkalemia (5.8 +/- 0.8 mM)" [OMIM:Hyperkalemia (5.8 +/- 0.8 mM)]
OMIM: "Hyperkalemia (6.4 +/- 0.7 mM)" [OMIM:Hyperkalemia (6.4 +/- 0.7 mM)]
OMIM: "Hyperkalemia (7.5 +/- 0.9 mM)" [OMIM:Hyperkalemia (7.5 +/- 0.9 mM)]
OMIM: "Hyperkalemia (>6.2 mM in both dominant and recessive)" [OMIM:Hyperkalemia (>6.2 mM in both dominant and recessive)]
UMLS:C0020461 "HYPERKALAEMIA" [HPO:0002153]
UMLS:C0020461 "Hyperkalemia" [Orphanet:49160]
Is a (Direct Parents):
Orphanet Abnormality of metabolism/homeostasis
MedDRA Potassium imbalance
HPO         Abnormality of potassium homeostasis
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)
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)