403522004: Subcutaneous morphea (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Autoimmune skin disease\Localised scleroderma\Subcutaneous morphoea
• \Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Autoimmune skin disease\Localised scleroderma\Subcutaneous morphoea
• \General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Autoimmune skin disease\Localised scleroderma\Subcutaneous morphoea
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Autoimmune skin disease\Localised scleroderma\Subcutaneous morphoea
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \Integumentary system finding\Skin finding\Disorder of skin (disorder)\Autoimmune skin disease\Localised scleroderma\Subcutaneous morphoea
• \Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of immune function (disorder)\Autoimmune disease\Autoimmune connective tissue disorder\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.\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of immune function (disorder)\Autoimmune disease\Autoimmune skin disease\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Autoimmune skin disease\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of connective tissue\Autoimmune connective tissue disorder\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.\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Autoimmune skin disease\Localised scleroderma\Subcutaneous morphoea
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Induration of skin\Sclerosis of the skin\Morphoea\Localised scleroderma\Subcutaneous morphoea

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1773731011	Subcutaneous morphoea	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1775017018	Subcutaneous morphea	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2688416010	Subcutaneous morphea (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1771448010	Subcutaneous morphoea (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1773731011	Subcutaneous morphoea	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1773731011	Subcutaneous morphoea	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1775017018	Subcutaneous morphea	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1775017018	Subcutaneous morphea	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2688416010	Subcutaneous morphea (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2688416010	Subcutaneous morphea (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5263601000241111	morphée sous-cutanée	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5263601000241111	morphée sous-cutanée	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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