773333003: Autosomal systemic lupus erythematosus (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Inherited disorder of connective tissue\Autosomal systemic lupus erythematosus
• \Autosomal hereditary disorder\Autosomal systemic lupus erythematosus
• \Disorder of immune function\Autoimmune disease\...
• \Autoimmune connective tissue disorder\Autosomal systemic lupus erythematosus
• \Lupus erythematosus\Systemic lupus erythematosus\Autosomal systemic lupus erythematosus
• \Disorder of connective tissue\Inherited disorder of connective tissue\Autosomal systemic lupus erythematosus
• \Disorder of connective tissue\Autoimmune connective tissue disorder\Autosomal systemic lupus erythematosus
• \Disorder of connective tissue\Lupus erythematosus\Systemic lupus erythematosus\Autosomal systemic lupus erythematosus
• \Disorder of connective tissue\Collagen disease\Systemic lupus erythematosus\Autosomal systemic lupus erythematosus

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3723216017	Autosomal systemic lupus erythematosus (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3723217014	Autosomal systemic lupus erythematosus	en	Synonym	Active	Case insensitive	SNOMED CT core
3723218016	Autosomal SLE (systemic lupus erythematosus)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3723219012	Familial systemic lupus erythematosus	en	Synonym	Active	Case insensitive	SNOMED CT core
3723220018	A rare genetic multisystemic chronic autoimmune disease characterized by the presence of systemic lupus erythematosus symptoms in two or more members of a single family. Patients present a wide spectrum of clinical manifestations, including cutaneous (malar rash, photosensitivity), ocular (keratoconjunctivitis sicca, retinopathy), gastrointestinal (oral ulceration, abdominal pain), cardiac (atherosclerosis, chest pain), pulmonary (serositis, pleurisy), musculoskeletal (arthralgia, myalgia), renal (nephritis, hematuria), obstetrical (increased spontaneous abortions, neonatal lupus), constitutional (fatigue, loss of appetite) and neuropsychiatric (mood and cognitive disorders) involvement, amongst others.	en	Definition	Active	Case sensitive	SNOMED CT core
3723221019	A rare genetic multisystemic chronic autoimmune disease characterised by the presence of systemic lupus erythematosus symptoms in two or more members of a single family. Patients present a wide spectrum of clinical manifestations, including cutaneous (malar rash, photosensitivity), ocular (keratoconjunctivitis sicca, retinopathy), gastrointestinal (oral ulceration, abdominal pain), cardiac (atherosclerosis, chest pain), pulmonary (serositis, pleurisy), musculoskeletal (arthralgia, myalgia), renal (nephritis, haematuria), obstetrical (increased spontaneous abortions, neonatal lupus), constitutional (fatigue, loss of appetite) and neuropsychiatric (mood and cognitive disorders) involvement, amongst others.	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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