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
Schistocytosis	Schistocyte
Schistocytosis	Schistocytosis (finding)
Schistocytosis	Schistocytosis (finding)
Schistocytosis	Schistocyte
Schistosoma bovis (& [infection])	Schistosoma bovis
Schistosoma haematobium (& vesical schistosomiasis)	Schistosoma haematobium
Schistosoma intercalatum	Schistosoma intercalatum
Schistosoma japonicum	Schistosoma japonicum
Schistosoma japonicum infection	Schistosoma japonicum infection
Schistosoma mansoni (& intestinal schistosomiasis)	Schistosoma mansoni (organism)
Schistosoma mansoni (& intestinal schistosomiasis)	Intestinal schistosomiasis
Schistosoma mattheii (& [infection])	Schistosoma mattheei
Schistosoma species	Schistosoma
Schistosoma spindale	Schistosoma spindale
Schistosomiasis of bladder	Schistosoma haematobium infection
Schistosomiasis of bladder	Cystitis with bilharziasis (disorder)
Schistosomiasis: [bilharziasis] or [pulmonary]	Pulmonary schistosomiasis
Schistosomiasis: [bilharziasis] or [pulmonary]	Infection by Schistosoma
Schizophrenia: [other] or [cenesthopathic]	Coenesthopathic schizophrenia
Schizophrenic child	History of schizophrenia in child of subject (situation)
Schizophrenic psychoses (& [paranoid schizophrenia])	Paranoid schizophrenia
Schizophrenic psychoses	Paranoid schizophrenia
Schizophrenic psychoses (& [paranoid schizophrenia])	Schizophrenia
Schizophyllum commune	Clitocybe clavipes
Schizophyllum commune	Schizophyllum commune
Schneiderian papilloma	Transitional cell papilloma, benign
Schneiderian papilloma	Benign sinonasal papilloma (morphologic abnormality)
Schprintzen	A rare genetic disorder characterized by craniosynostosis, craniofacial and skeletal abnormalities, marfanoid habitus, cardiac anomalies, neurological abnormalities, and intellectual disability.
Schultz disease	Agranulocytosis
Schwartz syndrome	Syndrome of inappropriate vasopressin secretion
Sciatic nerve and its branches	Entire sciatic nerve
Sciatic nerve and its branches	Structure of sciatic nerve
Sciatic nerve lesion	Sciatic nerve lesion
Sciatic nerve lesion	Sciatic nerve palsy
Sciatic nerve lesion	Sciatic neuropathy
Sclera &/or iris operations	Operative procedure on sclera
Sclera &/or iris operations	Operative procedure on iris
Sclera and iris operations	Operative procedure on sclera
Sclera and iris operations	Operative procedure on iris
Sclera and iris operations NOS	Operative procedure on iris
Sclera and iris operations NOS	Operative procedure on sclera
Scleral buckling: [explant HFQ] or [Arruga for detachment]	Buckling of sclera using explant
Scleral plug, reusable	Scleral plug
Scleral plug, single-use	Scleral plug
Sclerema neonatorum	Sclerema neonatorum
Sclerema neonatorum	Subcutaneous fat necrosis of newborn
Scleritis &/or episcleritis	Episcleritis
Scleritis &/or episcleritis	Scleritis
Scleritis &/or episcleritis	Scleritis and episcleritis
Scleritis &/or episcleritis	Scleritis and episcleritis
Scleritis &/or episcleritis	Episcleritis
Scleritis &/or episcleritis	Scleritis
Scleroderma (& [acrosclerosis] or [systemic sclerosis])	Systemic sclerosis with limited cutaneous involvement
Scleroderma (& [acrosclerosis] or [systemic sclerosis])	Sclerodactyly
Scleroderma (& [acrosclerosis] or [systemic sclerosis])	Systemic sclerosis
Scleroderma (& [acrosclerosis] or [systemic sclerosis])	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.
Scleroderma (& [systemic sclerosis])	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.
Scleroderma (& [systemic sclerosis])	Systemic sclerosis
Scleroderma (& [systemic sclerosis])	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.
Scleroderma (& [systemic sclerosis])	Systemic sclerosis
Scleroderma	Genus Scleroderma (fungus) (organism)
Scleroderma	Sclerodermus
Scleroderma in newborn	Systemic sclerosis
Scleroderma in newborn	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.
Scleroderma in newborn	Localised scleroderma
Scleroderma in newborn	A rare secondary neonatal autoimmune disease characterized by neonatal onset of erythematous skin lesions with a linear appearance that gradually become indurated and hyperpigmented and progressively present skin atrophy. Positive serum antibodies (in particular antinuclear antibodies and/or rheumatoid factor) may be associated.
Scleroderma species	Sclerodermus
Scleroderma species	Genus Scleroderma (fungus) (organism)
Scleroderma variant	Localised scleroderma
Scleroderma variant	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.
Scleroderma variant	Systemic sclerosis
Scleroderma with multisystem involvement	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.
Scleroderma with multisystem involvement	Systemic sclerosis
Scleroderma with organ / system involvement	Systemic sclerosis
Scleroderma with organ / system involvement	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.
Sclerosing injection	Injection of sclerosing agent
Sclerosing injection (& vein (& varicose))	Injection of sclerosing agent in vein
Sclerosing injection (& vein (& varicose))	Injection of sclerosing agent in varicose vein
Sclerosing injection (& vein (& varicose))	Injection of sclerosing agent
Sclerosing lymphangitis of penis	Sclerosing lymphangitis of penis
Sclerosing lymphangitis of penis	Mondor's phlebitis of the penis
Sclerostomy	Cautery sclerostomy
Sclerostomy	Sclerostomy
Sclerotherapy endoscopic needle, single-use	Sclerotherapy endoscopic needle
Scolecobasidium species	Scolecobasidium
Scopulariopsis species	Scopulariopsis
Scots pine pollen allergen	Scots pine pollen
Scratch of head and neck	Scratch of neck (finding)
Scratch of head and neck	Scratch of head
Screech owl	Genus Megascops (organism)
Screech owl	Genus Otus (organism)
Screened - abnormality	Abnormal finding on screening procedure (finding)
Screening (& [health check])	Screening procedure
Screening (& [health check])	Screening - health check
Screening - general	Screening procedure
Screening - general	Screening procedure
Screening for diabetes	Diabetes mellitus screening
Screening for drug abuse	Screening for harmful pattern of substance use (procedure)
Screening for malignant neoplasm excluding cervical	Screening for malignant neoplastic disease (procedure)
Screening invite - ? address	Questionable if screening invite sent to correct address (finding)
Screening invite - ? address	Questionable if screening invite sent to correct address (finding)

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Reference Sets

Reference set descriptor

Description inactivation indicator reference set

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)