771300001: Hereditary progressive mucinous histiocytosis (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Chronic disease of skin\Hereditary progressive mucinous histiocytosis
• \General finding of soft tissue\Skin finding\Disorder of skin\Chronic disease of skin\Hereditary progressive mucinous histiocytosis
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Chronic disease of skin\Hereditary progressive mucinous histiocytosis
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Hereditary progressive mucinous histiocytosis
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Chronic disease of skin\Hereditary progressive mucinous histiocytosis
• \Integumentary system finding\Skin finding\Disorder of skin\Chronic disease of skin\Hereditary progressive mucinous histiocytosis
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary progressive mucinous histiocytosis
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary progressive mucinous histiocytosis
• \Disease\Disorder of haematopoietic morphology\Histiocytosis\Chronic histiocytosis\Hereditary progressive mucinous histiocytosis
• \Disease\Disorder of haematopoietic morphology\Histiocytosis\Non-Langerhans cell histiocytic dermatosis\Hereditary progressive mucinous histiocytosis
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary progressive mucinous histiocytosis
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Hereditary progressive mucinous histiocytosis
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Chronic disease of skin\Hereditary progressive mucinous histiocytosis
• \Disease\Chronic disease\Chronic histiocytosis\Hereditary progressive mucinous histiocytosis
• \Disease\Chronic disease\Chronic disease of skin\Hereditary progressive mucinous histiocytosis
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Chronic disease of skin\Hereditary progressive mucinous histiocytosis

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3705539018	Hereditary progressive mucinous histiocytosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3705540016	Hereditary progressive mucinous histiocytosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3705541017	A rare benign non-Langerhans cell histiocytosis characterized by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-colored to red-brown papules with predilection for the face, dorsal hands, forearms and legs, without associated mucosal or visceral involvement. Histologically, papules are well-circumscribed, unencapsulated, nodular aggregates of histiocytes with abundant mucin in the upper and mid dermis.	en	Definition	Active	Case sensitive	SNOMED CT core
3705542012	A rare benign non-Langerhans cell histiocytosis characterised by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-coloured to red-brown papules with predilection for the face, dorsal hands, forearms and legs, without associated mucosal or visceral involvement. Histologically, papules are well-circumscribed, unencapsulated, nodular aggregates of histiocytes with abundant mucin in the upper and mid dermis.	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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