Elevated serum creatinine

Symptom Information:

Symptom ID: HPO:0003259
Synonyms:
Elevated creatinine [HPO:0003259]
Increased creatinine [HPO:0003259]
Increased serum creatinine [HPO:0003259]
Elevated creatinine [OMIM:Elevated creatinine]
Elevated serum creatinine [OMIM:Elevated serum creatinine]
Increased creatinine [OMIM:Increased creatinine]
Increased serum creatinine [OMIM:Increased serum creatinine]
Quality:
Cross references:
OMIM: "Elevated creatinine" [OMIM:Elevated creatinine]
OMIM: "Elevated serum creatinine" [OMIM:Elevated serum creatinine]
OMIM: "Increased creatinine" [OMIM:Increased creatinine]
OMIM: "Increased serum creatinine" [OMIM:Increased serum creatinine]
Is a (Direct Parents):
HPO         Abnormal circulating creatinine level
HPO         Azotemia
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:
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)