Dehydration

Symptom Information:

Symptom ID: HPO:0001944
Synonyms:
Dehydration (disorder) [Orphanet:54280]
Dehydration [Orphanet:54280]
Dehydration [OMIM:Dehydration]
Dehydration/hydroelectrolytic loss [Orphanet:54280]
Dehydration [MedDRA:10012174]
Fluid loss [MedDRA:10012174]
Hypotonic dehydration [MedDRA:10012174]
Water excessive loss of [MedDRA:10012174]
Exsiccosis [MedDRA:10012174]
Isotonic dehydration [MedDRA:10012174]
Hypertonic dehydration [MedDRA:10012174]
Quality:
Cross references:
Orphanet:54280 "Dehydration/hydroelectrolytic loss" [Orphanet:54280]
OMIM: "Dehydration" [OMIM:Dehydration]
UMLS:C0011175 "Dehydration" [HPO:0001944]
UMLS:C0011175 "Dehydration" [Orphanet:54280]
Is a (Direct Parents):
HPO         Abnormality of fluid regulation
MedDRA Total fluid volume decreased
Orphanet Health status anomalies
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of fluid regulation(HPO:0011032)
             Dehydration(HPO:0001944)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Electrolyte and fluid balance conditions(MedDRA:10014412)
       Total fluid volume decreased(MedDRA:10044084)
          Dehydration(HPO:0001944)
Database Frequency: 59 / 7739
Resource:

All diseases associated with this symptom:

ADRENAL HYPOPLASIA, CONGENITAL (OMIM:300200)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal recessive distal renal tubular acidosis without deafness (Orphanet:93609)
Autosomal recessive infantile hypercalcemia (Orphanet:300547)
Autosomal recessive polycystic kidney disease (Orphanet:731)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
Bartter syndrome (Orphanet:112)
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY (OMIM:203400)
CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY (OMIM:610600)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Central diabetes insipidus (Orphanet:178029)
Cholera (Orphanet:173)
Chronic hiccup (Orphanet:396)
Classic Bartter syndrome (Orphanet:93605)
Combined malonic and methylmalonic acidemia (Orphanet:289504)
Congenital chloride diarrhea (Orphanet:53689)
Congenital lactase deficiency (Orphanet:53690)
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (Orphanet:83620)
Cystic fibrosis (Orphanet:586)
Cystinosis (Orphanet:213)
DIABETES MELLITUS, TRANSIENT NEONATAL, 1 (OMIM:601410)
Epidermolysis bullosa simplex with pyloric atresia (Orphanet:158684)
Familial cold urticaria (Orphanet:47045)
Familial hypoaldosteronism (Orphanet:427)
Fanconi renotubular syndrome 1 (OMIM:134600)
Fanconi syndrome - ichthyosis - dysmorphism (Orphanet:1981)
Generalized pseudohypoaldosteronism type 1 (Orphanet:171876)
HYPERCHLORHIDROSIS, ISOLATED (OMIM:143860)
Harlequin ichthyosis (Orphanet:457)
Hypouricemia, renal, 1 (OMIM:220150)
Isobutyryl-CoA dehydrogenase deficiency (Orphanet:79159)
Isovaleric acidemia (Orphanet:33)
Junctional epidermolysis bullosa (Orphanet:305)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
Ketoacidosis due to beta-ketothiolase deficiency (Orphanet:134)
Lamellar ichthyosis (Orphanet:313)
MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY (OMIM:602199)
Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency (Orphanet:308425)
Methylmalonic acidemia without homocystinuria (Orphanet:293355)
Microvillous inclusion disease (Orphanet:2290)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Neonatal diabetes mellitus (Orphanet:224)
Netherton syndrome (Orphanet:634)
Oculocerebrorenal syndrome (Orphanet:534)
Propionic acidemia (Orphanet:35)
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia (Orphanet:3390)
Renal pseudohypoaldosteronism type 1 (Orphanet:171871)
Reticular dysgenesis (Orphanet:33355)
Transient neonatal diabetes mellitus (Orphanet:99886)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)
Vitamin B12-responsive methylmalonic acidemia (Orphanet:28)
Vitamin B12-responsive methylmalonic acidemia type cblA (Orphanet:79310)
Vitamin B12-responsive methylmalonic acidemia type cblB (Orphanet:79311)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)
Yellow fever (Orphanet:99829)