Decreased urine output
Symptom Information:
| Symptom ID: | HPO:0011037 | ||
| 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 the genitourinary system(HPO:0000119) Abnormality of the urinary system(HPO:0000079) Abnormality of the urinary system physiology(HPO:0011277) Abnormal renal physiology(HPO:0012211) Abnormality of renal excretion(HPO:0011036) Abnormal urine output(HPO:0012590) Decreased urine output(HPO:0011037) Abnormality of the upper urinary tract(HPO:0010935) Abnormality of the kidney(HPO:0000077) Abnormal renal physiology(HPO:0012211) Abnormality of renal excretion(HPO:0011036) Abnormal urine output(HPO:0012590) Decreased urine output(HPO:0011037) MedDRA: |
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| Database Frequency: | 47 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Acquired central diabetes insipidus | (Orphanet:95626) |
| Acromegaly | (Orphanet:963) |
| Acute intermittent porphyria | (Orphanet:79276) |
| Adenine phosphoribosyltransferase deficiency | (Orphanet:976) |
| Adult polyglucosan body disease | (Orphanet:206583) |
| Alexander disease | (Orphanet:58) |
| Amelogenesis imperfecta - nephrocalcinosis | (Orphanet:1031) |
| Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
| Autosomal recessive medullary cystic kidney disease | (Orphanet:655) |
| Bartter syndrome | (Orphanet:112) |
| Botulism | (Orphanet:1267) |
| Central diabetes insipidus | (Orphanet:178029) |
| Chronic mucocutaneous candidiasis | (Orphanet:1334) |
| Congenital central diabetes insipidus | (Orphanet:95501) |
| Congenital primary megaureter | (Orphanet:617) |
| Cutaneous mastocytosis | (Orphanet:66646) |
| Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
| Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
| Dystrophic epidermolysis bullosa | (Orphanet:303) |
| Erdheim-Chester disease | (Orphanet:35687) |
| Foodborne botulism | (Orphanet:228371) |
| Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
| Generalized dominant dystrophic epidermolysis bullosa | (Orphanet:231568) |
| Hemorrhagic fever - renal syndrome | (Orphanet:340) |
| Hereditary central diabetes insipidus | (Orphanet:30925) |
| Hinman syndrome | (Orphanet:84085) |
| Inhalational botulism | (Orphanet:254504) |
| Junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:89840) |
| Lyell syndrome | (Orphanet:537) |
| Malakoplakia | (Orphanet:556) |
| Microscopic polyangiitis | (Orphanet:727) |
| Multiple endocrine neoplasia type 2 | (Orphanet:653) |
| Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
| Ochoa syndrome | (Orphanet:2704) |
| Oculocerebrorenal syndrome | (Orphanet:534) |
| Pseudomyxoma peritonei | (Orphanet:26790) |
| Rift valley fever | (Orphanet:319251) |
| Scleroderma | (Orphanet:801) |
| Septo-optic dysplasia | (Orphanet:3157) |
| Small cell carcinoma of the bladder | (Orphanet:284400) |
| Spastic paraplegia type 2 | (Orphanet:99015) |
| Stevens-Johnson syndrome | (Orphanet:36426) |
| Systemic capillary leak syndrome | (Orphanet:188) |
| Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
| Williams syndrome | (Orphanet:904) |
| Wound botulism | (Orphanet:178475) |
| Yellow fever | (Orphanet:99829) |