193252005: Myopathy due to scleroderma (disorder)

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

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Myopathy due to scleroderma

\Muscle finding (finding)\Disorder of muscle\...

\Disorder of skeletal muscle\Myopathy due to scleroderma

\Secondary myopathy\Myopathy due to scleroderma

\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Myopathy due to scleroderma

\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Myopathy due to scleroderma
\Disease\Disorder of muscle\Disorder of skeletal muscle\Myopathy due to scleroderma
\Disease\Disorder of muscle\Secondary myopathy\Myopathy due to scleroderma
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Myopathy due to scleroderma

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

297644019 Myopathy due to scleroderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

577118019 Myopathy due to scleroderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

297644019 Myopathy due to scleroderma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

297644019 Myopathy due to scleroderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

577118019 Myopathy due to scleroderma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

577118019 Myopathy due to scleroderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2837579013 Myopathy due to systemic sclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2837579013 Myopathy due to systemic sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4852161000241116 myopathie due à une sclérodermie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4852161000241116 myopathie due à une sclérodermie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Myopathy due to scleroderma	Is a	Myopathy	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Myopathy due to scleroderma	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Myopathy due to scleroderma	Is a	Disorder of skeletal muscle	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Myopathy due to scleroderma	Due to	sclérodermie	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Myopathy due to scleroderma	Associated with	Systemic sclerosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Myopathy due to scleroderma	Due to	A rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and sometimes other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc). Localized scleroderma is the cutaneous form of scleroderma characterized by fibrosis of the skin causing cutaneous plaques (morphea) or strips (linear scleroderma). Systemic sclerosis (SSc) is a generalized disorder characterized by fibrosis and vascular obliteration in the skin and organs, particularly, lungs, heart, and digestive tract. The exact cause of scleroderma is unknown. The disease originates from an autoimmune reaction, which leads to localized overproduction of collagen. In some cases, the condition is associated with exposure to chemicals. Other suggested causes include genetic and infectious mechanisms.	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Myopathy due to scleroderma	Is a	Secondary myopathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Disorder of skeletal muscle due to systemic sclerosis (disorder)	Is a	True	Myopathy due to scleroderma	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets