1222681008: Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome
• \Disorder of immune function\Autoimmune disease\Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome

Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5048484011	Tripeptidyl-peptidase II deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5048485012	TRIANGLE (TPPII-related immunodeficiency, autoimmunity, neurodevelopmental delay, impaired glycolysis, lysosomal expansion) disease	en	Synonym	Active	Case sensitive	SNOMED CT core
5048486013	TPPII-related immunodeficiency, autoimmunity and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease	en	Synonym	Active	Case sensitive	SNOMED CT core
5048487016	Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5048488014	Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
5048489018	TPPII (tripeptidyl-peptidase II) deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
5048490010	Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
5048491014	Evans syndrome associated with primary immunodeficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
5048492019	A rare genetic immune disease with characteristics of infantile or childhood onset of combined immunodeficiency with recurrent viral, bacterial, and fungal infections, severe autoimmunity mainly manifesting as antibody-mediated destruction of red blood cells, platelets and neutrophils and mild to moderate developmental delay. Laboratory findings include decreased circulating T-, B-, and natural killer cells, and hypergammaglobulinaemia.	en	Definition	Active	Case sensitive	SNOMED CT core
5048493012	A rare genetic immune disease with characteristics of infantile or childhood onset of combined immunodeficiency with recurrent viral, bacterial, and fungal infections, severe autoimmunity mainly manifesting as antibody-mediated destruction of red blood cells, platelets and neutrophils and mild to moderate developmental delay. Laboratory findings include decreased circulating T-, B-, and natural killer cells, and hypergammaglobulinemia.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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