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900000000000523009: POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Association type\Historical association reference set (foundation metadata concept)\POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT model component module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

900000000001150016 POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

900000000001151017 POSSIBLY EQUIVALENT TO association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
[X]Excessive sexual drive (& [nymphomania] or [satyriasis])	Excessive sexual drive
[X]Mixed anxiety and depressive disorder (& mild anxiety depression)	Mixed anxiety and depressive disorder
[X]Personality disorder: [emotionally unstable] or [aggressive] or [borderline] or [explosive]	Emotionally unstable personality disorder
[X]Sequelae of other specified infectious and parasitic diseases	Post-infectious disorder
[X]Sequelae of unspecified infectious and parasitic disease	Post-infectious disorder
[X]Sibling: [rivalry disorder] or [jealousy]	Sibling jealousy
[X]Specific developmental disorder of motor function (& [co-ordination disorder] or [dyspraxia] or [clumsy child syndrome])	Apraxia, developmental
[X]Specific developmental disorder of motor function (& [co-ordination disorder] or [dyspraxia] or [clumsy child syndrome])	Developmental coordination disorder
[X]Specific developmental disorder of motor function (& [co-ordination disorder] or [dyspraxia] or [clumsy child syndrome])	Developmental disorder of motor function
[X]Teicoplanin adverse reaction	Teicoplanin adverse reaction
[X]Teicoplanin adverse reaction	Teicoplanin adverse reaction
[X]Topical hydrocortisone adverse reaction	Allergy to hydrocortisone (finding)
[X]Topical hydrocortisone adverse reaction	Hydrocortisone adverse reaction (disorder)
[X]Topical hydrocortisone adverse reaction	Hypersensitivity to hydrocortisone (finding)
[X]Topical hydrocortisone adverse reaction	Hypersensitivity to hydrocortisone (finding)
[X]Topical hydrocortisone adverse reaction	Allergy to hydrocortisone (finding)
[X]Topical hydrocortisone adverse reaction	Hydrocortisone adverse reaction (disorder)
[X]solvents: [mental & behavioural disorders dependence syndrome due to use of] or [drug addiction]	Glue sniffing dependence (disorder)
a	Tumor staging descriptor a (tumor staging)
a.m. peak specimen	a.m. peak specimen (qualifier value)
beta>2< Glycoprotein	Apolipoprotein H
cryotherapy of lesion of palate (procedure)	Cryotherapy of palate
cryotherapy of lesion of palate (procedure)	Cryotherapy to lesion of palate
min	minute (qualifier value)
p	Tumor staging descriptor p (tumor staging)
p.m. trough specimen	p.m. trough specimen (qualifier value)
pH observations	pH - finding
pyrilamine maleate+benzocaine	Product containing benzocaine and mepyramine (medicinal product)
r	Tumor staging descriptor r (tumor staging)
ther specified pulmonary tuberculosis (disorder)	Pulmonary tuberculosis
von Hippel internal corneal ulcer	Irido-corneo-trabecular dysgenesis
von Willebrand disease, type 1^a^	Hereditary von Willebrand disease type 1
von Willebrand disease, type 1^a^	Hereditary von Willebrand disease type 1A
von Willebrand disease, type IIC	Hereditary von Willebrand disease type 2
von Willebrand disease, type IIC	Hereditary von Willebrand disease
von Willebrand disease, type IID	Hereditary von Willebrand disease
von Willebrand disease, type IID	Hereditary von Willebrand disease type 2
von Willebrand disease, type IIE	Hereditary von Willebrand disease
von Willebrand disease, type IIE	Hereditary von Willebrand disease type 2
von Willebrand disease, type IIF	Hereditary von Willebrand disease type 2
von Willebrand disease, type IIF	Hereditary von Willebrand disease
von Willebrand disease, type IIG	Hereditary von Willebrand disease type 2
von Willebrand disease, type IIG	Hereditary von Willebrand disease
von Willebrand disease, type IIH	Hereditary von Willebrand disease
von Willebrand disease, type IIH	Hereditary von Willebrand disease type 2
y	Tumor staging descriptor y (tumor staging)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001150016	POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001151017	POSSIBLY EQUIVALENT TO association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)