Thrombotic microangiopathy
Symptom Information:
Symptom ID: | MedDRA:10043645 | ||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477) Abnormal bleeding(HPO:0001892) Thrombotic microangiopathy(MedDRA:10043645) Vascular disorders(MedDRA:10047065) Vascular haemorrhagic disorders(MedDRA:10047075) Haemorrhages NEC(MedDRA:10018987) Abnormal bleeding(HPO:0001892) Thrombotic microangiopathy(MedDRA:10043645) Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) Coagulation and bleeding analyses(MedDRA:10009728) Abnormal bleeding(HPO:0001892) Thrombotic microangiopathy(MedDRA:10043645) |
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Database Frequency: | 11 / 7739 | ||
Resource: |
All diseases associated with this symptom:
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) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |
Typical hemolytic uremic syndrome | (Orphanet:90038) |