Autoimmune hemolytic anemia

Symptom Information:

Symptom ID: HPO:0001890
Synonyms:
Autoimmune haemolytic anaemia [HPO:0001890]
Hemolytic anemia, autoimmune [HPO:0001890]
Autoimmune hemolytic anemia [OMIM:Autoimmune hemolytic anemia]
Hemolytic anemia, autoimmune [OMIM:Hemolytic anemia, autoimmune]
Autoimmune haemolytic anaemia [MedDRA:10073785]
Quality:
Cross references:
OMIM: "Autoimmune hemolytic anemia" [OMIM:Autoimmune hemolytic anemia]
OMIM: "Hemolytic anemia, autoimmune" [OMIM:Hemolytic anemia, autoimmune]
Is a (Direct Parents):
MedDRA Blood autoimmune disorders
HPO         Autoimmunity
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)
                      Autoimmune hemolytic anemia(HPO:0001890)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Autoimmunity(HPO:0002960)
                Autoimmune hemolytic anemia(HPO:0001890)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Autoimmunity(HPO:0002960)
       Blood autoimmune disorders(MedDRA:10003817)
          Autoimmune hemolytic anemia(HPO:0001890)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

ANEMIA, AUTOIMMUNE HEMOLYTIC (OMIM:205700)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME (OMIM:601859)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA (OMIM:603909)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V (OMIM:616100)
Autoimmune lymphoproliferative syndrome (Orphanet:3261)
Combined immunodeficiency due to STIM1 deficiency (Orphanet:317430)
Hyper-IgM syndrome type 4 (Orphanet:101091)
IMMUNODEFICIENCY 17 (OMIM:615607)
IMMUNODEFICIENCY 31C (OMIM:614162)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome (Orphanet:37042)
Immunodeficiency due to CD25 deficiency (Orphanet:169100)
LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS (OMIM:247800)
Multiple intestinal atresia (Orphanet:2300)
Nijmegen breakage syndrome (Orphanet:647)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)