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


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-May 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5048484011 Tripeptidyl-peptidase II deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
5048485012 TRIANGLE (TPPII-related immunodeficiency, autoimmunity, neurodevelopmental delay, impaired glycolysis, lysosomal expansion) disease en Synonym Active Entire term case sensitive SNOMED CT core module
5048486013 TPPII-related immunodeficiency, autoimmunity and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease en Synonym Active Entire term case sensitive SNOMED CT core module
5048487016 Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5048488014 Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5048489018 TPPII (tripeptidyl-peptidase II) deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
5048490010 Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5048491014 Evans syndrome associated with primary immunodeficiency en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome Is a Combined immunodeficiency disease true Inferred relationship Existential restriction modifier
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome Pathological process Autoimmune process true Inferred relationship Existential restriction modifier 1
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome Is a Autoimmune disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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