Oliguria
Symptom Information:
Symptom ID: | HPO:0100520 | ||||||||||||||||||||||
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) Oliguria(HPO:0100520) 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) Oliguria(HPO:0100520) MedDRA: Investigations(MedDRA:10022891) Renal and urinary tract investigations and urinalyses(MedDRA:10038362) Urinary tract function analyses NEC(MedDRA:10049179) Oliguria(HPO:0100520) Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal failure and impairment(MedDRA:10038443) Oliguria(HPO:0100520) |
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Database Frequency: | 14 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Alström syndrome | (Orphanet:64) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Cushing syndrome | (Orphanet:553) |
Cystinosis | (Orphanet:213) |
Hypouricemia, renal, 1 | (OMIM:220150) |
Hypouricemia, renal, 2 | (OMIM:612076) |
Left ventricular noncompaction 10 | (OMIM:615396) |
MELAS | (Orphanet:550) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Neonatal hemochromatosis | (Orphanet:446) |
Peripartum cardiomyopathy | (Orphanet:563) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Senior-Loken syndrome 7 | (OMIM:613615) |