1264010001: Primary hypereosinophilic syndrome (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\Disorder of hematopoietic cell proliferation (disorder)\Hypereosinophilic syndrome\Primary hypereosinophilic syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5170888014	Primary hypereosinophilic syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5170889018	Primary hypereosinophilic syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5170890010	Clonal hypereosinophilic syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5170891014	Neoplastic hypereosinophilic syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5170893012	Primary HES (hypereosinophilic syndrome)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5170894018	HES-N - hypereosinophilic syndrome neoplastic	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400469019	A rare hypereosinophilic syndrome characterized by hypereosinophilia produced by clonal eosinophils derived from neoplastic stem cells in the absence of any secondary cause of eosinophilia and persisting for at least six months. The condition is associated with signs of organ infiltration, dysfunction, and damage. Clinical manifestations are highly variable, depending on the organ systems involved, and include dermatologic, pulmonary, cardiac, gastrointestinal, and cerebral manifestations, among others.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400470018	A rare hypereosinophilic syndrome characterised by hypereosinophilia produced by clonal eosinophils derived from neoplastic stem cells in the absence of any secondary cause of eosinophilia and persisting for at least six months. The condition is associated with signs of organ infiltration, dysfunction, and damage. Clinical manifestations are highly variable, depending on the organ systems involved, and include dermatologic, pulmonary, cardiac, gastrointestinal, and cerebral manifestations, among others.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

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