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
Hepatitis A+typhoid vaccine	Hepatitis A virus antigen-containing vaccine product
Hepatitis B contact	Exposure to Hepatitis B virus (event)
Hepatitis B core antigen test	Hepatitis B core antigen measurement
Hepatitis B core antigen test	Hepatitis B core antigen measurement
Hepatitis B core antigen test	Hepatitis B core antigen measurement
Hepatitis B immunoglobulin allergy	Allergy to Hepatitis b surface antigen immunoglobulin
Hepatitis B vaccine (adult) 20micrograms/mL injection solution 1mL vial	Hepatitis B surface antigen only vaccine product
Hepatitis B vaccine 10micrograms/0.5mL pediatric injection vial	Hepatitis B surface antigen only vaccine product
Hepatitis B vaccine 10micrograms/1mL injection	Hepatitis B virus antigen-containing vaccine product
Hepatitis B vaccine 10micrograms/mL injection suspension 1mL prefilled syringe	Hepatitis B virus antigen-containing vaccine product
Hepatitis B vaccine 10micrograms/mL injection suspension 1mL vial	Hepatitis B virus antigen-containing vaccine product
Hepatitis B vaccine 20micrograms/mL injection suspension 1ml prefilled syringe	Hepatitis B surface antigen only vaccine product
Hepatitis B vaccine 40micrograms/mL injection suspension 1ml vial	Hepatitis B virus antigen-containing vaccine product
Hepatitis B virus recombinant vaccine	Hepatitis B virus antigen-containing vaccine product
Hepatitis B virus recombinant vaccine	Hepatitis B virus antigen-containing vaccine product
Hepatitis B virus vaccine	Hepatitis B virus antigen-containing vaccine product
Hepatitis B virus vaccine	Hepatitis B virus antigen-containing vaccine product
Hepatitis E antibody level	Hepatitis E antibody measurement
Hepatitis a vaccine, inactiv 25unt suspension	Hepatitis A virus antigen-containing vaccine product
Hepatitis a vaccine, inactiv 25unts solution	Hepatitis A virus antigen-containing vaccine product
Hepatitis a vaccine, inactiv 50unt suspension	Hepatitis A virus antigen-containing vaccine product
Hepatitis a vaccine, inactiv 50unts solution	Hepatitis A virus antigen-containing vaccine product
Hepatitis: [viral (infectious) A] or [infective]	Viral hepatitis, type A
Hepatitis: [viral (infectious) A] or [infective]	Acute type A viral hepatitis
Hepatobiliary ductal system imaging including gallbladder	Radionuclide imaging of hepatobiliary region with gallbladder stimulation (procedure)
Hepatopexy (& [Binnie] or [Kerr])	Hepatopexy
Hepatotomy: [OS] or [Little] or [Stromeyer]	Incision of liver
Hepcidin	Hepcidin 25 peptide (substance)
Hepcidin	Prohepcidin
Herbaspirillum species	Herbaspirillum
Herbicide or fungicide	Fungicide
Herbicide or fungicide	Herbicide
Hereditary &/or degenerative CNS disease	Hereditary degenerative disease of central nervous system
Hereditary &/or degenerative CNS disease	Hereditary degenerative disease of central nervous system
Hereditary &/or degenerative CNS disease	Degenerative disease of the central nervous system
Hereditary &/or degenerative CNS disease	Degenerative disease of the central nervous system
Hereditary AND/OR degenerative disease of central nervous system	Degenerative disease of the central nervous system
Hereditary AND/OR degenerative disease of central nervous system	Hereditary degenerative disease of central nervous system
Hereditary and degenerative diseases of the central nervous system	Hereditary degenerative disease of central nervous system
Hereditary and degenerative diseases of the central nervous system	Degenerative disease of the central nervous system
Hereditary and degenerative diseases of the central nervous system NOS	Hereditary degenerative disease of central nervous system
Hereditary and degenerative diseases of the central nervous system NOS	Degenerative disease of the central nervous system
Hereditary and degenerative diseases of the central nervous system NOS	Hereditary degenerative disease of central nervous system
Hereditary and degenerative diseases of the central nervous system NOS	Degenerative disease of the central nervous system
Hereditary and idiopathic peripheral neuropathy	Hereditary peripheral neuropathy
Hereditary and idiopathic peripheral neuropathy	Idiopathic peripheral neuropathy
Hereditary benign intraepithelial dyskeratosis	Hypoplastic enamel-onycholysis-hypohidrosis syndrome (disorder)
Hereditary benign intraepithelial dyskeratosis	Hereditary benign intraepithelial dyskeratosis (disorder)
Hereditary diffuse mesangial proliferative glomerulonephritis	Nephrotic syndrome, diffuse mesangial proliferative glomerulonephritis
Hereditary diffuse mesangial proliferative glomerulonephritis	Dense deposit disease (disorder)
Hereditary disease in family possibly affecting fetus	Family history of hereditary disease (situation)
Hereditary disease in family possibly affecting fetus	Fetal hereditary disease suspected
Hereditary disorder of hematologic system	Hereditary disorder of cellular element of blood (disorder)
Hereditary disturbances in tooth structure	Hereditary disorder of tooth
Hereditary edema of legs	Hereditary lymphedema
Hereditary edema of legs	Hereditary lymphedema type I (disorder)
Hereditary edema of legs	Hereditary lymphedema
Hereditary edema of legs	Hereditary lymphedema type I (disorder)
Hereditary epistaxis	Bleeding from nose
Hereditary epistaxis	Hereditary disease
Hereditary hypertyrosinemia	Hereditary hypertyrosinemia
Hereditary hypertyrosinemia	Adverse reaction to ganglion blocking drug
Hereditary hypertyrosinemia	Deficiency of fumarylacetoacetase
Hereditary inflammatory disorder involving skin	Hereditary periodic fever (disorder)
Hereditary lentiginosis	Familial generalised lentiginosis
Hereditary lentiginosis	Noonan's syndrome
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary myositis ossificans	Progressive myositis ossificans
Hereditary nephritis	Thin basement membrane disease
Hereditary nephropathy not elsewhere classified	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, dense deposit disease	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse crescentic glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse endocapillary proliferative glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse membranous glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse mesangial proliferative glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse mesangiocapillary glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, focal and segmental glomerular lesions	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, minor glomerular abnormality	Hereditary nephropathy (disorder)
Hereditary optic atrophy: [NOS] or [Leber's]	Leber's optic atrophy
Hereditary or idiopathic disturbance of tooth structure	Idiopathic erosion of teeth
Hereditary or idiopathic disturbance of tooth structure	Idiopathic resorption of root of tooth (disorder)
Hereditary or idiopathic disturbance of tooth structure	Hereditary disorder of tooth
Hereditary or idiopathic peripheral neuropathy NOS	Idiopathic peripheral neuropathy
Hereditary or idiopathic peripheral neuropathy NOS	Hereditary peripheral neuropathy
Hereditary sensory and autonomic neuropathy, type I	Hereditary sensory and autonomic neuropathy type I (disorder)
Hereditary sensory and autonomic neuropathy, type I	Charcot-Marie-Tooth disease, type I (disorder)
Hereditary sensory and autonomic neuropathy, type II	Charcot-Marie-Tooth disease, type II (disorder)
Hereditary sensory and autonomic neuropathy, type II	Hereditary sensory and autonomic neuropathy type II (disorder)
Hereditary sensory and autonomic neuropathy, type II	Hereditary insensitivity to pain with anhidrosis
Hereditary sideroblastic anemia	X chromosome-linked sideroblastic anemia
Hereditary tooth structure disturbances NEC	Tooth disorder
Hereditary tooth structure disturbances NEC	Hereditary disorder of tooth

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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)