Hyponatremia
Symptom Information:
Symptom ID: | HPO:0002902 | |||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||
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 sodium homeostasis(HPO:0010931) Hyponatremia(HPO:0002902) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Electrolyte and fluid balance conditions(MedDRA:10014412) Sodium imbalance(MedDRA:10041273) Hyponatremia(HPO:0002902) Investigations(MedDRA:10022891) Water, electrolyte and mineral investigations(MedDRA:10047843) Mineral and electrolyte analyses(MedDRA:10027637) Hyponatremia(HPO:0002902) |
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Database Frequency: | 37 / 7739 | |||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ADRENAL HYPOPLASIA, CONGENITAL | (OMIM:300200) |
AICA-ribosiduria | (Orphanet:250977) |
Acute intermittent porphyria | (Orphanet:79276) |
BARTTER SYNDROME, TYPE 4A | (OMIM:602522) |
BARTTER SYNDROME, TYPE 4B | (OMIM:613090) |
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY | (OMIM:203400) |
CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY | (OMIM:610600) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Central diabetes insipidus | (Orphanet:178029) |
Congenital chloride diarrhea | (Orphanet:53689) |
Cystinosis | (Orphanet:213) |
Cytomegalic congenital adrenal hypoplasia | (Orphanet:95702) |
Familial dysautonomia | (Orphanet:1764) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Familial hypoaldosteronism | (Orphanet:427) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Gaucher disease type 2 | (Orphanet:77260) |
Generalized pseudohypoaldosteronism type 1 | (Orphanet:171876) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
HYPERCHLORHIDROSIS, ISOLATED | (OMIM:143860) |
HYPOADRENOCORTICISM, FAMILIAL | (OMIM:240200) |
Hereditary coproporphyria | (Orphanet:79273) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Infant botulism | (Orphanet:178478) |
Infantile Bartter syndrome with deafness | (Orphanet:89938) |
Kawasaki disease | (Orphanet:2331) |
Legionellosis | (Orphanet:549) |
MELAS | (Orphanet:550) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Nephrogenic syndrome of inappropriate antidiuresis | (Orphanet:93606) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Renal pseudohypoaldosteronism type 1 | (Orphanet:171871) |
Whipple disease | (Orphanet:3452) |
Wolfram syndrome 1 | (OMIM:222300) |