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
Joint effusion of the upper arm	Elbow joint effusion
Joint excluding knee	Joint structure
Joint excluding knee	Entire joint
Joint function	Joint movement
Joint function	Joint mobilization
Joint mice in joint, excluding the knee	Loose body in joint
Joint mobilization	Range of joint movement normal
Joint mobilization	Joint mobilization
Joint of lower leg or tarsus	Tibiofibular joint structure
Joint of lower leg or tarsus	Ankle joint structure
Joint of lower leg or tarsus NEC	Ankle joint structure
Joint pain: [shoulder] or [acromioclavicular]	Shoulder joint pain
Joint pain: [shoulder] or [acromioclavicular]	Shoulder joint pain
Joint pain: [shoulder] or [acromioclavicular]	Pain of acromioclavicular joint
Joint pain: [shoulder] or [acromioclavicular]	Pain of acromioclavicular joint
Joint probing (& [diagnostic])	Joint probing
Joint problem	Joint function disorder
Joint problem	Finding of range of joint movement
Joint reconstruction: [other arthroplasty] or [resurfacing]	Resurfacing arthroplasty
Joint structure of lower leg and/or tarsus	Ankle joint structure
Joint structure of lower leg and/or tarsus	Tibiofibular joint structure
Joint structure of pelvic girdle	Structure of joint of pelvic wall
Joint: [pain - arthralgia] or [ache]	Pain of joint (finding)
Jonesia species	Jonesia
Judaism	Judaism
Judaism	Jewish, follower of religion (person)
Jugular vein injury: [external] or [NOS]	Injury of external jugular vein
Jumping disease	Jumping disease
Jumping mouse	Family Dipodidae (organism)
Jumping mouse	Subfamily Zapodinae (organism)
Junctional epidermolysis bullosa	Junctional epidermolysis bullosa gravis of Herlitz (disorder)
Junctional epidermolysis bullosa	Junctional epidermolysis bullosa (disorder)
Junctional epidermolysis bullosa gravis of Herlitz	Junctional epidermolysis bullosa (disorder)
Junctional epidermolysis bullosa gravis of Herlitz	Junctional epidermolysis bullosa (disorder)
Junctional epidermolysis bullosa gravis of Herlitz	Junctional epidermolysis bullosa gravis of Herlitz (disorder)
Junctional epidermolysis bullosa gravis of Herlitz	Junctional epidermolysis bullosa gravis of Herlitz (disorder)
June grass pollen allergen	June grass pollen
Juniper pollen allergen	Juniper pollen
Juvenile chronic polyarthritis	Juvenile seronegative polyarthritis (disorder)
Juvenile chronic polyarthritis	Polyarticular juvenile idiopathic arthritis
Juvenile fucosidosis	Juvenile fucosidosis (disorder)
Juvenile fucosidosis	Adult fucosidosis (disorder)
Juvenile osteochondritis hip &/or pelvis	Hip juvenile osteochondropathy
Juvenile osteochondritis hip &/or pelvis	Juvenile osteochondritis of the hip and pelvis
Juvenile osteochondritis hip &/or pelvis	Pelvis juvenile osteochondropathy
Juvenile osteochondritis of the arm &/or hand	Juvenile osteochondritis of the arm and hand
Juvenile osteochondritis of the arm &/or hand	Juvenile osteochondritis of the hand
Juvenile osteochondritis of the arm &/or hand	Juvenile osteochondritis of the arm
Juvenile osteochondrosis of capitellum of humerus	Juvenile osteochondrosis of head of humerus
Juvenile osteochondrosis of capitellum of humerus	Juvenile osteochondrosis of capitulum of humerus (disorder)
Juvenile osteochondrosis of hip AND/OR pelvis	Juvenile osteochondritis of the hip and pelvis
Juvenile osteochondrosis of hip AND/OR pelvis	Juvenile osteochondrosis of pelvis
Juvenile osteochondrosis of lower extremity	Juvenile osteochondrosis of lower extremity, excluding foot
Juvenile osteochondrosis of lower extremity	Juvenile osteochondrosis of lower extremity (disorder)
Juvenile osteochondrosis of the leg	Juvenile osteochondrosis of lower extremity (disorder)
Juvenile osteopathia patellae	Juvenile osteochondrosis of the secondary patellar center
Juvenile pemphigoid	Childhood bullous pemphigoid (disorder)
Juvenile rheumatoid arthritis &/or Still's disease	Juvenile idiopathic arthritis (disorder)
Juvenile rheumatoid arthritis &/or Still's disease	Systemic onset juvenile chronic arthritis
Juvenile rheumatoid arthritis &/or Still's disease	Systemic onset juvenile chronic arthritis
Juvenile rheumatoid arthritis &/or Still's disease	Juvenile idiopathic arthritis (disorder)
Juvenile scleroderma	Morphea
Juvenile scleroderma	A rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and sometimes other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc). Localized scleroderma is the cutaneous form of scleroderma characterized by fibrosis of the skin causing cutaneous plaques (morphea) or strips (linear scleroderma). Systemic sclerosis (SSc) is a generalized disorder characterized by fibrosis and vascular obliteration in the skin and organs, particularly, lungs, heart, and digestive tract. The exact cause of scleroderma is unknown. The disease originates from an autoimmune reaction, which leads to localized overproduction of collagen. In some cases, the condition is associated with exposure to chemicals. Other suggested causes include genetic and infectious mechanisms.
Juvenile scleroderma	Systemic sclerosis
Juvenile xanthogranuloma	Xanthoma disseminatum (disorder)
Juvenile xanthogranuloma	Juvenile xanthogranuloma (disorder)
Juvenile xanthogranuloma	Multiple eruptive juvenile xanthogranuloma (disorder)
Juvenile: [dermatitis herpetiformis] or [pemphigoid]	Childhood bullous pemphigoid (disorder)
Juxtacortical osteosarcoma	Parosteal osteosarcoma (morphologic abnormality)
Juxtacortical osteosarcoma	Periosteal osteosarcoma
Juxtacortical osteosarcoma	Periosteal osteosarcoma
Juxtacortical osteosarcoma	Parosteal osteosarcoma (morphologic abnormality)
K wiring of fracture	Primary open reduction of fragment of bone and fixation using wire system
K wiring of fracture	Fixation of bone fragment using Kirschner wire
Kakapo	Genus Strigops (organism)
Kakapo	Strigops habroptila (organism)
Kalanchoe species	Genus Kalanchoe (organism)
Kandori's syndrome	Kandori fleck retina is a rare, genetic retinal dystrophy disorder characterized by irregular, sharply defined, yellowish-white lesions of variable size that are distributed mainly in the nasal equatorial region of the retina, with a tendency to confluence, that are not associated with any vascular or optic nerve abnormalities. They frequently manifest as mild and stationary night blindness.
Kaolin and pectin mixture	Kaolin (substance)
Kaolin and pectin mixture	Pectin
Kaolin+calcium carbonate 500mg/250mg/5mL junior suspension	Product containing precisely calcium carbonate 50 milligram/1 milliliter and light kaolin 100 milligram/1 milliliter conventional release oral suspension (clinical drug)
Kappa chain disease	Disorder of kidney due to kappa light chain disease (disorder)
Kappa chain disease	Kappa light chain disease
Karyotype 46, XX	Karyotype 46, XX (cell structure)
Karyotype 46, XY	Karyotype 46, XY (cell structure)
Kashin-Beck disease of the forearm	Kashin-Bek disease
Kashin-Beck disease of the lower leg	Kashin-Bek disease
Kashin-Beck disease of the upper arm	Kashin-Beck disease of the shoulder region (disorder)
Katayama fever	Schistosoma japonicum infection
Kentucky blue grass pollen allergen	Kentucky blue grass pollen
Kenya tick virus	Boutonneuse fever
Keratectomy for pterygium	Keratectomy for pterygium (procedure)
Keratectomy for pterygium	Simple excision of pterygium (procedure)
Keratitis &/or keratoconjunctivitis	Keratoconjunctivitis
Keratitis &/or keratoconjunctivitis	Keratitis
Keratoderma plantare sulcata	Pitted keratolysis
Keratoderma punctata	A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients.
Keratoderma punctata	Punctate palmoplantar keratoderma (disorder)
Keratoderma with deafness	Palmoplantar keratoderma-deafness syndrome is a keratinization disorder characterized by focal or diffuse palmoplantar keratoderma. A patchy distribution is observed with accentuation on the thenars, hypothenars and the arches of the feet. The disease becomes apparent in infancy and is associated with sensorineural hearing loss that shows a variable age of onset. Due to genetic and clinical similarities, it has been proposed that palmoplantar keratoderma-deafness syndrome, knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome and keratoderma hereditarium mutilans may represent variants of one broad disorder of syndromic deafness with heterogeneous phenotype. The disease is transmitted in an autosomal dominant manner with incomplete penetrance.
Keratome blade, reprocessed	Scalpel blade (physical object)
Keratome blade, reusable	Scalpel blade (physical object)

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Reference Sets

Reference set descriptor

Description inactivation indicator reference set

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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)