Acute kidney injury

Symptom Information:

Symptom ID: HPO:0001919
Synonyms:
Acute renal failure [HPO:0001919]
Acute renal failure [OMIM:Acute renal failure]
Renal failure acute [MedDRA:10038436]
Quality:
Cross references:
OMIM: "Acute renal failure" [OMIM:Acute renal failure]
Is a (Direct Parents):
HPO         Renal insufficiency
MedDRA Renal failure and impairment
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)
                   Renal insufficiency(HPO:0000083)
                      Acute kidney injury(HPO:0001919)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Renal insufficiency(HPO:0000083)
                         Acute kidney injury(HPO:0001919)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal failure and impairment(MedDRA:10038443)
          Acute kidney injury(HPO:0001919)
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

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 DGKE deficiency (Orphanet:357008)
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)
Autosomal dominant myoglobinuria (Orphanet:99846)
Genetic recurrent myoglobinuria (Orphanet:99845)
Hereditary renal hypouricemia (Orphanet:94088)
Hypouricemia, renal, 1 (OMIM:220150)
Hypouricemia, renal, 2 (OMIM:612076)
Immunoglobulin-mediated membranoproliferative glomerulonephritis (Orphanet:329903)
Kawasaki disease (Orphanet:2331)
Kelley-Seegmiller syndrome (Orphanet:79233)
Mulibrey nanism (Orphanet:2576)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Renal cysts and diabetes syndrome (Orphanet:93111)
Typical hemolytic uremic syndrome (Orphanet:90038)