771300001: histiocytose progressive mucineuse héréditaire (trouble)

SNOMED CT Concept\constatation clinique\...

\Skin AND/OR mucosa finding (finding)\Skin finding\affection de la peau (trouble)\maladie chronique de la peau\Hereditary progressive mucinous histiocytosis

\constatation générale à propos des tissus mous\Skin finding\affection de la peau (trouble)\maladie chronique de la peau\Hereditary progressive mucinous histiocytosis
\constatation générale à propos des tissus mous\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\maladie chronique de la peau\Hereditary progressive mucinous histiocytosis

\Integumentary system finding\troubles tégumentaires\Hereditary disorder of the integument\Hereditary progressive mucinous histiocytosis
\Integumentary system finding\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\maladie chronique de la peau\Hereditary progressive mucinous histiocytosis
\Integumentary system finding\Skin finding\affection de la peau (trouble)\maladie chronique de la peau\Hereditary progressive mucinous histiocytosis

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary progressive mucinous histiocytosis
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary progressive mucinous histiocytosis
\Disease\trouble de la morphologie hématopoïétique\syndrome histiocytaire\Chronic histiocytosis\Hereditary progressive mucinous histiocytosis
\Disease\trouble de la morphologie hématopoïétique\syndrome histiocytaire\Non-Langerhans cell histiocytic dermatosis (disorder)\Hereditary progressive mucinous histiocytosis
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary progressive mucinous histiocytosis
\Disease\affection d'un système corporel\troubles tégumentaires\Hereditary disorder of the integument\Hereditary progressive mucinous histiocytosis
\Disease\affection d'un système corporel\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\maladie chronique de la peau\Hereditary progressive mucinous histiocytosis
\Disease\maladie chronique\Chronic histiocytosis\Hereditary progressive mucinous histiocytosis
\Disease\maladie chronique\maladie chronique de la peau\Hereditary progressive mucinous histiocytosis
\Disease\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\maladie chronique de la peau\Hereditary progressive mucinous histiocytosis

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

3705539018 Hereditary progressive mucinous histiocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3705540016 Hereditary progressive mucinous histiocytosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

770471000241114 histiocytose progressive mucineuse héréditaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

942501000172119 histiocytose progressive mucineuse héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary progressive mucinous histiocytosis	évolution clinique (attribut)	progressif	true	Inferred relationship	Some	2
Hereditary progressive mucinous histiocytosis	est un(e) (attribut)	maladie chronique de la peau	true	Inferred relationship	Some
Hereditary progressive mucinous histiocytosis	localisation d'une constatation (attribut)	structure de la peau	true	Inferred relationship	Some	1
Hereditary progressive mucinous histiocytosis	est un(e) (attribut)	Hereditary disorder of the integument	true	Inferred relationship	Some
Hereditary progressive mucinous histiocytosis	morphologie associée (attribut)	Mucinous histiocytosis	true	Inferred relationship	Some	1
Hereditary progressive mucinous histiocytosis	est un(e) (attribut)	Non-Langerhans cell histiocytic dermatosis (disorder)	true	Inferred relationship	Some
Hereditary progressive mucinous histiocytosis	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hereditary progressive mucinous histiocytosis	est un(e) (attribut)	Chronic histiocytosis	true	Inferred relationship	Some

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
3705539018	Hereditary progressive mucinous histiocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3705540016	Hereditary progressive mucinous histiocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
770471000241114	histiocytose progressive mucineuse héréditaire (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
942501000172119	histiocytose progressive mucineuse héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
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	Entire term case sensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core