FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

900000000000523009: 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)

49567 members. Search Members:

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] Somatoform autonomic dysfunction (& named variants) Psychogenic dysuria (disorder)
[X] Somatoform autonomic dysfunction (& named variants) Psychogenic diarrhea
[X] Somatoform autonomic dysfunction (& named variants) Somatoform autonomic dysfunction of gastrointestinal tract (disorder)
[X] Somatoform autonomic dysfunction (& named variants) Psychogenic hyperventilation
[X] Somatoform autonomic dysfunction (& named variants) Somatoform autonomic dysfunction
[X] Somatoform autonomic dysfunction (& named variants) Neurocirculatory asthenia (disorder)
[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 dysmenorrhoea
[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]) Dyslalia
[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]) 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]) 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 coordination disorder
[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]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 Allergy to hydrocortisone (finding)
[X]Topical hydrocortisone adverse reaction Hydrocortisone adverse reaction (disorder)
[X]Topical hydrocortisone adverse reaction Hypersensitivity to hydrocortisone (finding)
[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 (substance)
cryotherapy of lesion of palate (procedure) Cryotherapy of palate
cryotherapy of lesion of palate (procedure) Cryotherapy to lesion 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-observationer pH - finding
pyrilaminmaleat + benzocain Product containing benzocaine and mepyramine (medicinal product)
r Tumor staging descriptor r (tumor staging)
ther specified pulmonary tuberculosis (disorder) Pulmonary tuberculosis
leukoma adhaerens Irido-corneo-trabecular dysgenesis
von Willebrands sygdom, type 1^a^ A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). The type 1 disease is considered to be the most common form of VWD, caused by mutations in the VWF gene (12p13.3). Transmitted in an autosomal dominant manner.
von Willebrands sygdom, type 1^a^ Hereditary von Willebrand disease type 1A
von Willebrands sygdom type IIC A form of von Willebrand disease (VWD) with characteristics of 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. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive.
von Willebrands sygdom 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 Willebrands sygdom type IID A form of von Willebrand disease (VWD) with characteristics of 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. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive.
von Willebrands sygdom 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 Willebrands sygdom 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 Willebrands sygdom type IIE A form of von Willebrand disease (VWD) with characteristics of 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. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive.
von Willebrands sygdom, 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 Willebrands sygdom, type IIF A form of von Willebrand disease (VWD) with characteristics of 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. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive.
von Willebrands sygdom type IIG A form of von Willebrand disease (VWD) with characteristics of 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. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive.
von Willebrands sygdom 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 Willebrands sygdom 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).
von Willebrands sygdom type IIH A form of von Willebrand disease (VWD) with characteristics of 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. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive.
y Tumor staging descriptor y (tumor staging)

Start Previous Page 496 of 496

Reference Sets

Reference set descriptor

Back to Start