Thrombotic microangiopathy

Symptom Information:

Symptom ID: MedDRA:10043645
Synonyms:
Thrombotic microangiopathy [OMIM:Thrombotic microangiopathy]
Thrombotic microangiopathy (hyaline thrombi of platelets and fibrin in terminal arterioles and capillaries) [OMIM:Thrombotic microangiopathy (hyaline thrombi of platelets and fibrin in terminal arterioles and capillaries)]
Quality:
Cross references:
OMIM: "Thrombotic microangiopathy" [OMIM:Thrombotic microangiopathy]
OMIM: "Thrombotic microangiopathy (hyaline thrombi of platelets and fibrin in terminal arterioles and capillaries)" [OMIM:Thrombotic microangiopathy (hyaline thrombi of platelets and fibrin in terminal arterioles and capillaries)]
Is a (Direct Parents):
MedDRA Abnormal bleeding
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)
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Coagulation and bleeding analyses(MedDRA:10009728)
          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)
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)