1231732006: Smoldering systemic mastocytosis (disorder)

• SNOMED CT Concept\constatation clinique\Disease\...
• \trouble de la morphologie hématopoïétique\néoplasme des mastocytes\Systemic mast cell disease (disorder)\Smoldering systemic mastocytosis
• \néoplasme et/ou hamartome\maladie néoplasique\Neoplasm of hematopoietic cell type (disorder)\néoplasme des mastocytes\Systemic mast cell disease (disorder)\Smoldering systemic mastocytosis
• \maladie systémique\Systemic mast cell disease (disorder)\Smoldering systemic mastocytosis
• \maladie chronique\Smoldering systemic mastocytosis

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5074053017	Smoldering systemic mastocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5074054011	Smouldering systemic mastocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5074055012	Smoldering systemic mastocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5074064019	SSM - smoldering systemic mastocytosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5074065018	SSM - smouldering systemic mastocytosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5074062015	A rare slowly progressive form of systemic mastocytosis (SM) with characteristics of gradual accumulation of neoplastic mast cells in the visceral organs. Patients typically present with splenomegaly, hypercellular marrow and in most cases urticaria pigmentosa-like skin lesions. Although the aetiology is not fully understood, an activating mutation of KIT, usually KIT D816V, is found in the mast cells of virtually all cases. This mutation probably accounts for the abnormal accumulation of mast cells in organs/tissues.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5074063013	A rare slowly progressive form of systemic mastocytosis (SM) with characteristics of gradual accumulation of neoplastic mast cells in the visceral organs. Patients typically present with splenomegaly, hypercellular marrow and in most cases urticaria pigmentosa-like skin lesions. Although the etiology is not fully understood, an activating mutation of KIT, usually KIT D816V, is found in the mast cells of virtually all cases. This mutation probably accounts for the abnormal accumulation of mast cells in organs/tissues.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada French language reference set (foundation metadata concept)

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