Elevated serum creatinine
Symptom Information:
Symptom ID: | HPO:0003259 | |||||||
Synonyms: |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of nitrogen compound homeostasis(HPO:0004364) Azotemia(HPO:0002157) Elevated serum creatinine(HPO:0003259) Abnormal circulating creatinine level(HPO:0012100) Elevated serum creatinine(HPO:0003259) MedDRA: |
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Database Frequency: | 31 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Argininemia | (Orphanet:90) |
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) |
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia | (Orphanet:34149) |
Autosomal dominant progressive nephropathy with hypertension | (Orphanet:88659) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Citrullinemia type I | (Orphanet:247525) |
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency | (Orphanet:93583) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Fabry disease | (Orphanet:324) |
Familial dysautonomia | (Orphanet:1764) |
Hypouricemia, renal, 1 | (OMIM:220150) |
Hypouricemia, renal, 2 | (OMIM:612076) |
INTERSTITIAL NEPHRITIS, KARYOMEGALIC | (OMIM:614817) |
Ichthyosis - intellectual deficit - dwarfism - renal impairment | (Orphanet:2278) |
MEDULLARY CYSTIC KIDNEY DISEASE 1 | (OMIM:174000) |
Nephronophthisis 2 | (OMIM:602088) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Short-rib thoracic dysplasia 5 with or without polydactyly | (OMIM:614376) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |
Tubulointerstitial nephritis and uveitis syndrome | (Orphanet:91500) |
Typical hemolytic uremic syndrome | (Orphanet:90038) |
Wilson disease | (Orphanet:905) |