Hypokalemia

Symptom Information:

Symptom ID: HPO:0002900
Synonyms:
Hypokalemia (disorder) [Orphanet:49140]
HYPOKALAEMIA [HPO:0002900]
Hypokalemia [Orphanet:49140]
Potassium Deficiency [Orphanet:49140]
Hypokalemia [OMIM:Hypokalemia]
Hypokalaemic syndrome [Orphanet:49140]
Potassium deficiency [Orphanet:49140]
Hypokalaemia [Orphanet:49140]
Hypokalaemic syndrome [MedDRA:10021017]
Hypokalemic syndrome [MedDRA:10021017]
Low potassium syndrome [MedDRA:10021017]
Syndrome hypokalemic [MedDRA:10021017]
Syndrome hypokalaemic [MedDRA:10021017]
Hypokalaemia [MedDRA:10021015]
Hypokalemia [MedDRA:10021015]
Hypopotassaemia [MedDRA:10021015]
Hypopotassemia [MedDRA:10021015]
Potassium deficiency [MedDRA:10021015]
Kaliopenia [MedDRA:10021015]
Hypokalemia (rare) [OMIM:Hypokalemia (rare)]
Quality:
Cross references:
Orphanet:49140 "Hypokalemia" [Orphanet:49140]
OMIM: "Hypokalemia" [OMIM:Hypokalemia]
OMIM: "Hypokalemia (rare)" [OMIM:Hypokalemia (rare)]
UMLS:C0020621 "HYPOKALAEMIA" [HPO:0002900]
UMLS:C0020621 "Hypokalemia" [Orphanet:49140]
UMLS:C0032827 "Potassium Deficiency" [Orphanet:49140]
Is a (Direct Parents):
HPO         Episodic hypokalemia
HPO         Abnormality of potassium homeostasis
MedDRA Potassium imbalance
Orphanet Abnormality of metabolism/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)
                      Hypokalemia(HPO:0002900)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Electrolyte and fluid balance conditions(MedDRA:10014412)
       Potassium imbalance(MedDRA:10036451)
          Hypokalemia(HPO:0002900)
Database Frequency: 45 / 7739
Resource:

All diseases associated with this symptom:

ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
Aldosterone-producing adenoma with seizures and neurological abnormalities (Orphanet:369929)
Apparent mineralocorticoid excess (Orphanet:320)
Argininosuccinic aciduria (Orphanet:23)
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)
Bartter syndrome with hypocalcemia (Orphanet:263417)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Classic Bartter syndrome (Orphanet:93605)
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (Orphanet:90795)
Congenital chloride diarrhea (Orphanet:53689)
Cronkhite-Canada syndrome (Orphanet:2930)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
Cystinosis (Orphanet:213)
DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE (OMIM:304900)
Dent disease type 1 (Orphanet:93622)
Dent disease type 2 (Orphanet:93623)
EAST syndrome (Orphanet:199343)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Familial hyperaldosteronism type 3 (Orphanet:251274)
Fanconi renotubular syndrome 1 (OMIM:134600)
Generalized juvenile polyposis/juvenile polyposis coli (Orphanet:329971)
Gitelman syndrome (Orphanet:358)
Glycogen storage disease due to GLUT2 deficiency (Orphanet:2088)
HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY (OMIM:241150)
HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2 (OMIM:613345)
Hyperkalemic periodic paralysis (Orphanet:682)
Hypokalemic periodic paralysis (Orphanet:681)
Hypouricemia, renal, 2 (OMIM:612076)
Infantile Bartter syndrome with deafness (Orphanet:89938)
Juvenile polyposis syndrome (Orphanet:2929)
Leprechaunism (Orphanet:508)
Liddle syndrome (Orphanet:526)
Oculocerebrorenal syndrome (Orphanet:534)
Primary Fanconi syndrome (Orphanet:3337)
Proximal renal tubular acidosis (Orphanet:47159)
RENAL TUBULAR ACIDOSIS III (OMIM:267200)
Rabson-Mendenhall syndrome (Orphanet:769)
Thyrotoxic periodic paralysis (Orphanet:79102)