Hypokalemia
Symptom Information:
Symptom ID: | HPO:0002900 | ||||||||||||||||||||
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) Hypokalemia(HPO:0002900) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Electrolyte and fluid balance conditions(MedDRA:10014412) Potassium imbalance(MedDRA:10036451) Hypokalemia(HPO:0002900) |
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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) |