Microangiopathic hemolytic anemia

Symptom Information:

Symptom ID: HPO:0001937
Synonyms:
Microangiopathic hemolytic anemia [OMIM:Microangiopathic hemolytic anemia]
Microangiopathic hemolytic anemia (Coomb negative) [OMIM:Microangiopathic hemolytic anemia (Coomb negative)]
Quality:
Cross references:
OMIM: "Microangiopathic hemolytic anemia" [OMIM:Microangiopathic hemolytic anemia]
OMIM: "Microangiopathic hemolytic anemia (Coomb negative)" [OMIM:Microangiopathic hemolytic anemia (Coomb negative)]
Is a (Direct Parents):
HPO         Hemolytic anemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of erythrocytes(HPO:0001877)
             Anemia(HPO:0001903)
                Anemia due to reduced life span of red cells(HPO:0011895)
                   Hemolytic anemia(HPO:0001878)
                      Microangiopathic hemolytic anemia(HPO:0001937)
MedDRA:
Database Frequency: 12 / 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)
Kasabach-Merritt syndrome (Orphanet:2330)
Thrombotic thrombocytopenic purpura (Orphanet:54057)
Typical hemolytic uremic syndrome (Orphanet:90038)