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] Nonorganic disorder of the sleep-wake schedule: [psychogenic inversion of circadian rhythm (including nyctohemeral rhythm and sleep rhythm)]	Non-organic disorder of the sleep-wake schedule
[X] Orgasmic dysfunction (& [inhibited] or [psychogenic anorgasmy])	Orgasm disorder
[X] Paranoid personality disorder (& [expansive] or [fanatic] or [querulant] or [sensitive])	Paranoid personality disorder
[X] Social anxiety disorder of childhood (avoidant disorder)	Avoidant disorder of childhood
[X] Somatoform autonomic dysfunction (& named variants)	Psychogenic diarrhea
[X] Somatoform autonomic dysfunction (& named variants)	Psychogenic pylorospasm (disorder)
[X] Somatoform autonomic dysfunction (& named variants)	Somatoform autonomic dysfunction
[X] Somatoform autonomic dysfunction (& named variants)	Neurocirculatory asthenia
[X] Somatoform autonomic dysfunction (& named variants)	Psychogenic dyspepsia
[X] Somatoform autonomic dysfunction (& named variants)	Somatoform autonomic dysfunction of gastrointestinal tract (disorder)
[X] Somatoform autonomic dysfunction (& named variants)	Psychogenic dysuria
[X] Somatoform autonomic dysfunction (& named variants)	Irritable bowel syndrome
[X] Somatoform autonomic dysfunction (& named variants)	Psychogenic hyperventilation (disorder)
[X] Somatoform autonomic dysfunction (& named variants)	Psychogenic hiccough
[X] Somatoform autonomic dysfunction (& named variants)	Psychogenic cough
[X] Somatoform disorders: [other] or [psychogenic dysmenorrhoea] or [globus hystericus] or [psychogenic pruritis] or [psychogenic torticollis] or [teeth-grinding]	Psychogenic pruritus
[X] Somatoform disorders: [other] or [psychogenic dysmenorrhoea] or [globus hystericus] or [psychogenic pruritis] or [psychogenic torticollis] or [teeth-grinding]	Psychogenic dysmenorrhea
[X] Specific (isolated) phobias (& [acrophobia] or [animal] or [claustrophobia] or [simple phobia])	Simple phobia
[X] Specific speech articulation disorder (& [developmental (& phonological)] or [dyslalia] or [functional] or [lalling])	Phonological disorder
[X] Specific speech articulation disorder (& [developmental (& phonological)] or [dyslalia] or [functional] or [lalling])	Lalling
[X] Specific speech articulation disorder (& [developmental (& phonological)] or [dyslalia] or [functional] or [lalling])	Articulatory dyspraxia
[X] Specific speech articulation disorder (& [developmental (& phonological)] or [dyslalia] or [functional] or [lalling])	Dyslalia
[X] Specific speech articulation disorder (& [developmental (& phonological)] or [dyslalia] or [functional] or [lalling])	Developmental articulation disorder (disorder)
[X] Specific spelling disorder (& [spelling retardation without reading disorder])	Specific spelling disorder
[X](Disinhibited attachment disorder of childhood) or (affectionless psychopathy) or (institutional syndrome)	Childhood disinhibited attachment disorder
[X](Lack or loss of sexual desire) or (frigidity) or (hypoactive sexual desire disorder) or (lack of libido)	Lack or loss of sexual desire
[X](Schizoaffective disorder, mixed type) or (cyclic schizophrenia) or (mixed schizophrenic and affective psychosis)	Schizoaffective disorder, mixed type
[X]Acute and transient psychotic disorder, unspecified (& [reactive psychosis (including brief NOS)])	Reactive psychoses
[X]Dementia: [multi-infarct] or [predominantly cortical]	Multi-infarct dementia
[X]Depression without psychotic symptoms: [recurrent: [major] or [manic-depressive psychosis, depressed type] or [vital] or [current severe episode]] or [endogenous]	Recurrent major depressive episodes
[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	A disorder that follows infection but is distinct from the infection itself and its usual manifestations
[X]Sequelae of unspecified infectious and parasitic disease	A disorder that follows infection but is distinct from the infection itself and its usual manifestations
[X]Sibling: [rivalry disorder] or [jealousy]	Sibling jealousy
[X]Specific developmental disorder of motor function (& [co-ordination disorder] or [dyspraxia] or [clumsy child syndrome])	Developmental disorder of motor function
[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]Teicoplanin adverse reaction	Teicoplanin adverse reaction
[X]Teicoplanin adverse reaction	Teicoplanin adverse reaction
[X]Topical hydrocortisone adverse reaction	Hypersensitivity to hydrocortisone (finding)
[X]Topical hydrocortisone adverse reaction	Hydrocortisone adverse reaction (disorder)
[X]Topical hydrocortisone adverse reaction	Allergy 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
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 to lesion of palate
cryotherapy of lesion of palate (procedure)	Cryotherapy of palate
min	A period of time equal to sixty seconds or a sixtieth of an hour.
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^	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF).
von Willebrand disease, type 1^a^	Hereditary von Willebrand disease type 1A
von Willebrand disease, type IIC	A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2).
von Willebrand disease, type IIC	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N.
von Willebrand disease, type IID	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N.
von Willebrand disease, type IID	A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2).
von Willebrand disease, type IIE	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N.
von Willebrand disease, type IIE	A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2).
von Willebrand disease, type IIF	A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2).
von Willebrand disease, type IIF	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N.
von Willebrand disease, type IIG	A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2).
von Willebrand disease, type IIG	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N.
von Willebrand disease, type IIH	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N.
von Willebrand disease, type IIH	A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2).
y	Tumor staging descriptor y (tumor staging)

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Reference Sets

Reference set descriptor

Back to Start

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)