771309000: Autosomal recessive lymphoproliferative disease (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary neoplastic syndrome\Autosomal recessive lymphoproliferative disease
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive lymphoproliferative disease
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Autosomal recessive lymphoproliferative disease
• \Disorder of haematopoietic morphology\Lymphoproliferative disorder\Autosomal recessive lymphoproliferative disease

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3705582017	Autosomal recessive lymphoproliferative disease (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3705584016	Autosomal recessive lymphoproliferative disease	en	Synonym	Active	Case insensitive	SNOMED CT core
3705585015	A rare combined T and B cell immunodeficiency with a predisposition to lymphoproliferative syndrome. It is characterised by persistent symptomatic Epstein-Barr viraemia and hypogammaglobulinaemia variably presenting with fever, lymphadenopathy and systemic inflammatory conditions including hepatitis, pneumonia and sepsis. It may be associated with lymphoma, haemophagocytic lymphohistiocytosis, and aplastic anaemia.	en	Definition	Active	Case sensitive	SNOMED CT core
3705586019	A rare combined T and B cell immunodeficiency with a predisposition to lymphoproliferative syndrome. It is characterized by persistent symptomatic Epstein-Barr viremia and hypogammaglobulinemia variably presenting with fever, lymphadenopathy and systemic inflammatory conditions including hepatitis, pneumonia and sepsis. It may be associated with lymphoma, hemophagocytic lymphohistiocytosis, and aplastic anemia.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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