773333003: autosomale systemische lupus erythematodes (aandoening)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Monogenic autoinflammatory syndrome (disorder)\Type I interferonopathy\Autosomal systemic lupus erythematosus (disorder)
\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Autosomal systemic lupus erythematosus (disorder)
\Genetic disease\Hereditary disease\Connective tissue hereditary disorder (disorder)\Autosomal systemic lupus erythematosus (disorder)
\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal systemic lupus erythematosus (disorder)

\Disorder of immune function (disorder)\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Type I interferonopathy\Autosomal systemic lupus erythematosus (disorder)
\Disorder of immune function (disorder)\Chronic disease of immune function (disorder)\Autosomal systemic lupus erythematosus (disorder)
\Disorder of immune function (disorder)\Hereditary disorder of immune system\Autosomal systemic lupus erythematosus (disorder)
\Disorder of immune function (disorder)\Autoimmune disease\Autoimmune connective tissue disorder\Autosomal systemic lupus erythematosus (disorder)
\Disorder of immune function (disorder)\Autoimmune disease\Lupus erythematosus\Systemic lupus erythematosus\Autosomal systemic lupus erythematosus (disorder)

\Disorder of body system\Disorder of immune structure (disorder)\Chronic disease of immune structure (disorder)\Autosomal systemic lupus erythematosus (disorder)
\Disorder of body system\Disorder of immune structure (disorder)\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Type I interferonopathy\Autosomal systemic lupus erythematosus (disorder)
\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Type I interferonopathy\Autosomal systemic lupus erythematosus (disorder)
\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Autosomal systemic lupus erythematosus (disorder)

\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Type I interferonopathy\Autosomal systemic lupus erythematosus (disorder)

\Disorder of connective tissue (disorder)\Connective tissue hereditary disorder (disorder)\Autosomal systemic lupus erythematosus (disorder)
\Disorder of connective tissue (disorder)\Autoimmune connective tissue disorder\Autosomal systemic lupus erythematosus (disorder)
\Disorder of connective tissue (disorder)\Lupus erythematosus\Systemic lupus erythematosus\Autosomal systemic lupus erythematosus (disorder)
\Disorder of connective tissue (disorder)\Collagen disease\Systemic lupus erythematosus\Autosomal systemic lupus erythematosus (disorder)

\Chronic disease\Chronic disease of immune structure (disorder)\Autosomal systemic lupus erythematosus (disorder)
\Chronic disease\Chronic disease of immune function (disorder)\Autosomal systemic lupus erythematosus (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core

3723217014 Autosomal systemic lupus erythematosus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3723218016 Autosomal SLE (systemic lupus erythematosus) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3723219012 Familial systemic lupus erythematosus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

6442551000146113 autosomale systemische lupus erythematodes nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6442561000146111 autosomale systemische lupus erythematodes (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6442571000146117 autosomale SLE nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6442581000146115 autosomale lupus erythematodes systemicus nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6442591000146118 autosomaal erfelijke systemische lupus erythematosus nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal systemic lupus erythematosus (disorder)	Is a	Connective tissue hereditary disorder (disorder)	true	Inferred relationship	Some
Autosomal systemic lupus erythematosus (disorder)	Occurrence	Childhood	false	Inferred relationship	Some	1
Autosomal systemic lupus erythematosus (disorder)	Is a	Systemic lupus erythematosus	true	Inferred relationship	Some
Autosomal systemic lupus erythematosus (disorder)	Pathological process (attribute)	Autoimmune process	true	Inferred relationship	Some	1
Autosomal systemic lupus erythematosus (disorder)	Finding site	Connective tissue structure	false	Inferred relationship	Some	1
Autosomal systemic lupus erythematosus (disorder)	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Autosomal systemic lupus erythematosus (disorder)	Is a	Autoimmune connective tissue disorder	true	Inferred relationship	Some
Autosomal systemic lupus erythematosus (disorder)	Is a	Type I interferonopathy	true	Inferred relationship	Some
Autosomal systemic lupus erythematosus (disorder)	Is a	Hereditary disorder of immune system	true	Inferred relationship	Some
Autosomal systemic lupus erythematosus (disorder)	Finding site	Connective tissue structure	true	Inferred relationship	Some	2
Autosomal systemic lupus erythematosus (disorder)	Finding site	Structure of immune system (body structure)	true	Inferred relationship	Some	1
Autosomal systemic lupus erythematosus (disorder)	Associated morphology	Inflammatory morphology (morphologic abnormality)	true	Inferred relationship	Some	1
Autosomal systemic lupus erythematosus (disorder)	Is a	Chronic disease of immune function (disorder)	true	Inferred relationship	Some
Autosomal systemic lupus erythematosus (disorder)	Is a	Chronic disease of immune structure (disorder)	true	Inferred relationship	Some
Autosomal systemic lupus erythematosus (disorder)	Clinical course	Chronic	true	Inferred relationship	Some	3
Autosomal systemic lupus erythematosus (disorder)	Pathological process (attribute)	Autoimmune process	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3723216017	Autosomal systemic lupus erythematosus (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3723217014	Autosomal systemic lupus erythematosus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3723218016	Autosomal SLE (systemic lupus erythematosus)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3723219012	Familial systemic lupus erythematosus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6442551000146113	autosomale systemische lupus erythematodes	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6442561000146111	autosomale systemische lupus erythematodes (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6442571000146117	autosomale SLE	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6442581000146115	autosomale lupus erythematodes systemicus	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6442591000146118	autosomaal erfelijke systemische lupus erythematosus	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
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	Entire term case sensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core