1231732006: Smoldering systemic mastocytosis (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Disorder of haematopoietic morphology\Mast cell neoplasm\Systemic mast cell disease\Smouldering systemic mastocytosis
• \Neoplasm and/or hamartoma\Neoplastic disease\Neoplasm of haematopoietic cell type\Mast cell neoplasm\Systemic mast cell disease\Smouldering systemic mastocytosis
• \Systemic disease\Systemic mast cell disease\Smouldering systemic mastocytosis
• \Chronic disease\Smouldering systemic mastocytosis

Status: current, Defined. Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5074053017	Smoldering systemic mastocytosis	en	Synonym	Active	Case insensitive	SNOMED CT core
5074054011	Smouldering systemic mastocytosis	en	Synonym	Active	Case insensitive	SNOMED CT core
5074055012	Smoldering systemic mastocytosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5074064019	SSM - smoldering systemic mastocytosis	en	Synonym	Active	Case sensitive	SNOMED CT core
5074065018	SSM - smouldering systemic mastocytosis	en	Synonym	Active	Case sensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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