Increased blood urea nitrogen
Symptom Information:
Symptom ID: | HPO:0003138 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) Increased blood urea nitrogen(HPO:0003138) MedDRA: |
||
Database Frequency: | 14 / 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 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) |
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency | (Orphanet:93583) |
Fabry disease | (Orphanet:324) |
Familial dysautonomia | (Orphanet:1764) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |
Typical hemolytic uremic syndrome | (Orphanet:90038) |
Wilson disease | (Orphanet:905) |