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1156250009: Hypereosinophilic syndrome (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4573069018 Hypereosinophilic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4573070017 Hypereosinophilic syndrome (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypereosinophilic syndrome Is a Chronic eosinophilic leukemia (morphologic abnormality) false Inferred relationship Some
Hypereosinophilic syndrome Is a Myeloid proliferation true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hypereosinophilic syndrome Associated morphology True Hypereosinophilic syndrome Inferred relationship Some 1
Idiopathic hypereosinophilic syndrome (morphologic abnormality) Is a True Hypereosinophilic syndrome Inferred relationship Some
Lymphocytic hypereosinophilic syndrome (disorder) Associated morphology True Hypereosinophilic syndrome Inferred relationship Some 1
Myeloproliferative hypereosinophilic syndrome (disorder) Associated morphology True Hypereosinophilic syndrome Inferred relationship Some 2
A rare hypereosinophilic syndrome characterized by hypereosinophilia produced by reactive/non-clonal eosinophils secondary to an underlying medical condition and persisting for at least six months. The disorder can derive from non-neoplastic conditions (such as chronic infections and infestations, allergic reactions, intoxications, or autoimmune and chronic inflammatory disorders) or from neoplasms including non-myeloid malignancies, among others. It is associated with signs of organ infiltration, dysfunction, and damage. Clinical manifestations are highly variable, depending on the organ systems involved, and most commonly include dermatologic, pulmonary, cardiac, gastrointestinal, and cerebral manifestations. Associated morphology True Hypereosinophilic syndrome Inferred relationship Some 1
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. Associated morphology True Hypereosinophilic syndrome Inferred relationship Some 1

This concept is not in any reference sets

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