773646003: Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Effect of exposure to physical force\Disorders of skin caused by physical agents\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Effect of exposure to physical force\General effects of low temperature\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\...
• \Disorders of skin caused by physical agents\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Oedema\Disorder characterised by oedema\...
• \Angioedema and/or urticaria\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \General finding of soft tissue\Skin finding\Disorder of skin\Disorders of skin caused by physical agents\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \General finding of soft tissue\Skin finding\Disorder of skin\Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Disorders of skin caused by physical agents\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \General finding of observation of patient\Temperature-associated finding\Body temperature finding\Abnormal body temperature\Body temperature above reference range\Febrile illness\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \General finding of observation of patient\General body state finding\Vital signs finding\Body temperature finding\Abnormal body temperature\Body temperature above reference range\Febrile illness\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Disorders of skin caused by physical agents\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Integumentary system finding\Skin finding\Disorder of skin\Disorders of skin caused by physical agents\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Integumentary system finding\Skin finding\Disorder of skin\Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Monogenic autoinflammatory syndrome\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Febrile illness\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of immune function\Autoinflammatory disease\Monogenic autoinflammatory syndrome\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of immune function\Hereditary disorder of immune system\Monogenic autoinflammatory syndrome\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of body system\Disorder of immune structure\Inflammatory disorder of immune system\Autoinflammatory disease\Monogenic autoinflammatory syndrome\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease\Monogenic autoinflammatory syndrome\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Monogenic autoinflammatory syndrome\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Disorders of skin caused by physical agents\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\General effects of low temperature\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease\Monogenic autoinflammatory syndrome\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder characterised by oedema\Angioedema and/or urticaria\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder characterised by oedema\Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Recurrent disease\Hereditary periodic fever\Cryopyrin associated periodic syndrome\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Disorders of skin caused by physical agents\Cold-induced dermatosis\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Oedematous skin\Urticaria\Urticaria due to cold\Familial cold urticaria\PLCG2-associated antibody deficiency and immune dysregulation

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3725358015	PLCG2-associated antibody deficiency and immune dysregulation	en	Synonym	Active	Case sensitive	SNOMED CT core
3725359011	PLCG2 (phospholipase C gamma 2) associated antibody deficiency and immune dysregulation	en	Synonym	Active	Case sensitive	SNOMED CT core
3725360018	Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3725361019	Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3725362014	FACU - familial atypical cold urticaria	en	Synonym	Active	Case sensitive	SNOMED CT core
3725363016	Familial cold urticaria with common variable immunodeficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3725364010	A rare hereditary immune deficiency with skin involvement characterized by early-onset cold urticaria after generalized exposure to cold air or evaporative cooling and not after contact with cold objects. Additional immunologic abnormalities are often present - antibody deficiency, recurrent infections, autoimmune disease and symptomatic allergic disease. Caused by heterozygous deletion within the PLCG2 gene on chromosome 16q23.	en	Definition	Active	Case sensitive	SNOMED CT core
3725365011	A rare hereditary immune deficiency with skin involvement characterised by early-onset cold urticaria after generalised exposure to cold air or evaporative cooling and not after contact with cold objects. Additional immunologic abnormalities are often present - antibody deficiency, recurrent infections, autoimmune disease and symptomatic allergic disease. Caused by heterozygous deletion within the PLCG2 gene on chromosome 16q23.	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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