SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Disorder of immune function  414029004

Immunodeficiency disorder  234532001

Primary immune deficiency disorder  58606001

Combined immunodeficiency disease  442459007

Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome   1222681008

SNOMED CT code


SNOMED code1222681008
nameAutoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome
statusactive
date introduced2022-05-31
fully specified name(s)Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome (disorder)
synonyms
  • Tripeptidyl-peptidase II deficiency
  • TRIANGLE (TPPII-related immunodeficiency, autoimmunity, neurodevelopmental delay, impaired glycolysis, lysosomal expansion) disease
  • TPPII-related immunodeficiency, autoimmunity and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease
  • Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome
  • TPPII (tripeptidyl-peptidase II) deficiency
  • Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome
  • Evans syndrome associated with primary immunodeficiency
attributes - group1
Pathological processAutoimmune process   263680009
parents
  • Combined immunodeficiency disease   442459007
  • Autoimmune disease   85828009
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of immune function   414029004
        Immunodeficiency disorder   234532001
          Primary immune deficiency disorder   58606001
            Combined immunodeficiency disease   442459007
              Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome   1222681008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of immune function   414029004
        Autoimmune disease   85828009
          Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome   1222681008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome   1222681008

ancestors
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