783245001: Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
• \Disorder following clinical procedure\Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3758245015	Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3758246019	Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection	en	Synonym	Active	Case insensitive	SNOMED CT core
3780960019	Primary immunodeficiency with post-MMR (measles-mumps-rubella) vaccine viral infection	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3758248018	A rare primary immunodeficiency due to a defect in innate immunity disorder with characteristics of selective susceptibility to viral infections, particularly after systemic challenge with live viral vaccines such as the measles, mumps and rubella (MMR) vaccine. Patients present severe, potentially fatal, manifestations to viral illness, including encephalitis, hepatitis and pneumonitis.	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

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