Dehydration
Symptom Information:
Symptom ID: | HPO:0001944 | |||||||||||
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 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) |
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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) |