393573009: Hypereosinophilic syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Disorder of hematopoietic morphology\syndrome hyperéosinophilique

Status: current, 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

1487427015 Hypereosinophilic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2733923016 Hypereosinophilic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3866927017 HES - hypereosinophilic syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

1467634017 Hypereosinophilic syndrome en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1487427015 Hypereosinophilic syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1487427015 Hypereosinophilic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2733923016 Hypereosinophilic syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2733923016 Hypereosinophilic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3866927017 HES - hypereosinophilic syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

819071000241117 syndrome hyperéosinophilique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

819071000241117 syndrome hyperéosinophilique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
syndrome hyperéosinophilique	Is a	Neoplasm of hematopoietic cell type (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
syndrome hyperéosinophilique	Is a	Primary malignant neoplasm (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
syndrome hyperéosinophilique	Is a	Disorder of hematopoietic morphology	true	Inferred relationship	Existential restriction modifier (core metadata concept)
syndrome hyperéosinophilique	Associated morphology	Hypereosinophilic syndrome/chronic eosinophilic leukemia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
syndrome hyperéosinophilique	Associated morphology	Hypereosinophilic syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Idiopathic hypereosinophilic syndrome (disorder)	Is a	True	syndrome hyperéosinophilique	Inferred relationship	Existential restriction modifier (core metadata concept)
Lymphocytic hypereosinophilic syndrome (disorder)	Is a	True	syndrome hyperéosinophilique	Inferred relationship	Existential restriction modifier (core metadata concept)
Myeloproliferative hypereosinophilic syndrome	Is a	True	syndrome hyperéosinophilique	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypereosinophilic syndrome due to disease (disorder)	Is a	True	syndrome hyperéosinophilique	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary hypereosinophilic syndrome (disorder)	Is a	True	syndrome hyperéosinophilique	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set

SAME AS association reference set (foundation metadata concept)