Anuria
Symptom Information:
Symptom ID: | HPO:0100519 | ||||||||||||||||
Synonyms: |
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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 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) Anuria(HPO:0100519) 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) Anuria(HPO:0100519) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal failure and impairment(MedDRA:10038443) Anuria(HPO:0100519) |
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Database Frequency: | 20 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Alström syndrome | (Orphanet:64) |
Atypical hemolytic uremic syndrome | (Orphanet:2134) |
Atypical hemolytic uremic syndrome with B factor anomaly | (Orphanet:93578) |
Atypical hemolytic uremic syndrome with C3 anomaly | (Orphanet:93575) |
Atypical hemolytic uremic syndrome with H factor anomaly | (Orphanet:93579) |
Atypical hemolytic uremic syndrome with I factor anomaly | (Orphanet:93580) |
Atypical hemolytic uremic syndrome with MCP/CD46 anomaly | (Orphanet:93576) |
Atypical hemolytic uremic syndrome with anti-factor H antibodies | (Orphanet:93581) |
Atypical hemolytic uremic syndrome with thrombomodulin anomaly | (Orphanet:217023) |
Cushing syndrome | (Orphanet:553) |
Cystinosis | (Orphanet:213) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
MELAS | (Orphanet:550) |
Neonatal hemochromatosis | (Orphanet:446) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Renal tubular dysgenesis | (Orphanet:3033) |
Renal tubular dysgenesis of genetic origin | (Orphanet:97369) |
Senior-Loken syndrome 7 | (OMIM:613615) |
Typical hemolytic uremic syndrome | (Orphanet:90038) |