Hyponatremia

Symptom Information:

Symptom ID: HPO:0002902
Synonyms:
Serum hyponatremia [Orphanet:49080]
Sodium deficiency (disorder) [Orphanet:49080]
Hyponatremia (disorder) [Orphanet:49080]
Hyponatraemic [Orphanet:49080]
Hyponatremia [Orphanet:49080]
Hyponatremia [OMIM:Hyponatremia]
Hyponatraemia [Orphanet:49080]
Salt deficiency [Orphanet:49080]
Blood sodium decreased [Orphanet:49080]
Hyponatraemic syndrome [Orphanet:49080]
Hyponatraemia [MedDRA:10021036]
Hyponatremia [MedDRA:10021036]
Hyponatremic [MedDRA:10021036]
Na+ depletion [MedDRA:10021036]
Salt deficiency [MedDRA:10021036]
Salt depletion [MedDRA:10021036]
Sodium depletion [MedDRA:10021036]
Hyponatraemia aggravated [MedDRA:10021036]
Hyponatremia aggravated [MedDRA:10021036]
Hyponatraemic [MedDRA:10021036]
Blood sodium decreased [MedDRA:10005802]
Na+ reduced [MedDRA:10005802]
Sodium blood decreased [MedDRA:10005802]
Sodium decreased [MedDRA:10005802]
Sodium low [MedDRA:10005802]
Serum sodium decreased [MedDRA:10005802]
Hyponatraemic syndrome [MedDRA:10021037]
Low salt syndrome [MedDRA:10021037]
Low sodium syndrome [MedDRA:10021037]
Syndrome low salt [MedDRA:10021037]
Hyponatremic syndrome [MedDRA:10021037]
Quality:
Cross references:
Orphanet:49080 "Hyponatremia" [Orphanet:49080]
OMIM: "Hyponatremia" [OMIM:Hyponatremia]
UMLS:C0020625 "Hyponatremia" [HPO:0002902]
UMLS:C1971019 "Sodium deficiency (disorder)" [Orphanet:49080]
UMLS:C0857122 "Hyponatraemic" [Orphanet:49080]
UMLS:C0020625 "Hyponatremia" [Orphanet:49080]
Is a (Direct Parents):
HPO         Abnormality of sodium homeostasis
MedDRA Sodium imbalance
MedDRA Mineral and electrolyte analyses
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 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)
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)