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
Moving, function (observable entity)	Movement observable
Moving, function (observable entity)	Movement produced voluntarily by the patient.
Moxifloxacin	Product containing moxifloxacin (medicinal product)
Moxonidine 300micrograms tablet	Product containing precisely moxonidine 300 microgram/1 each conventional release oral tablet (clinical drug)
Moynahan's syndrome	Multiple lentigines syndrome
Moynahan's syndrome	A rare, genetic, epilepsy syndrome characterized by congenital alopecia, early-onset epilepsy, intellectual disability and speech delay. Large stature, delayed bone development and abnormal electroencephalogram have also been associated.
Mucopolysaccharidosis	Mucopolysaccharidosis
Mucopolysaccharidosis	Morquio syndrome
Mucopolysaccharidosis type I	Mucopolysaccharidosis, MPS-I-H/S
Mucopolysaccharidosis type I	Mucopolysaccharidosis, MPS-I
Mucopolysaccharidosis, MPS-IV-B	Mucopolysaccharidosis, MPS-IV-B
Mucopolysaccharidosis, MPS-IV-B	GM1 gangliosidosis
Mucopolysaccharidosis, type 1: (& [gargoylism] or [Hurler's syndrome] or [Scheie's syndrome])	Mucopolysaccharidosis, MPS-I-S
Mucopolysaccharidosis, type 1: (& [gargoylism] or [Hurler's syndrome] or [Scheie's syndrome])	Mucopolysaccharidosis, MPS-I-H
Mucopurulent conjunctivitis	Acute infectious conjunctivitis (disorder)
Mucor species	Genus Mucor (organism)
Mucormycosis antibody assay	Measurement of Mucor species antibody (procedure)
Mucosal flap (& operation)	Mucosal flap
Mucosal flap NOS	Reconstruction using mucosal flap (procedure)
Mucosal prolapse syndrome	Inflammatory cloacogenic polyp
Mucosal prolapse syndrome	Cap polyp
Mucosal prolapse syndrome	Internal intussusception of rectum
Mucositis following radiation therapy	Stomatitis due to and following radiation therapy
Mucositis necroticans agranulocytica	Agranulocytosis
Mucous membrane antibiotic	Antibacterial
Mucous membrane structure	Mucous membrane structure (body structure)
Mucous membrane structure	Mucosa, skin and subcutaneous material
Muellerius species	Muellerius
Mugged &/or homicide	Homicide
Mugwort pollen allergen	Mugwort pollen
Mulberry pollen allergen	Mulberry pollen
Multi-chamber venous compression system garment, reprocessed	Multiple chamber venous compression system garment
Multi-chamber venous compression system garment, reusable	Multiple chamber venous compression system garment
Multi-chamber venous compression system garment, single-use	Multiple chamber venous compression system garment
Multi-infarct state	Multi-infarct dementia
Multi-trace element supplement	Mineral supplement (substance)
Multi-trace element supplement therapy	Providing vitamins and minerals based on suboptimal food or fluid intake, iatrogenic deficiency or medical diagnosis.
Multicentric reticulohistiocytosis	Reticulohistiocytic granuloma
Multicentric reticulohistiocytosis	Lipoid dermatoarthritis
Multicepsosis	Infection by Taenia
Multicystic ovaries	Polycystic ovary
Multicystic ovaries	Polycystic ovary syndrome
Multifocal inner choroiditis	Punctate inner choroidopathy (disorder)
Multifocal inner choroiditis	Multifocal choroiditis (disorder)
Multilayer tablet	A solid single-dose preparation obtained by compressing uniform volumes of particulate solids or by extrusion or moulding. Tablets may be single layer tablets resulting from a single compression of particles and or multilayer tablets consisting of concentric or parallel layers obtained by successive compressions of particles of different composition.
Multilocular hydatid	Echinococcus multilocularis infection
Multilocular hydatid	Echinococcus multilocularis
Multiple and bilateral precerebral artery syndromes	Multiple AND bilateral precerebral artery obstruction
Multiple and bilateral precerebral artery syndromes	Multiple AND bilateral precerebral artery stenosis
Multiple boils	Boils of multiple sites
Multiple budding yeast	Finding of presence of multiple budding yeast
Multiple closed fractures involving both lower limbs, lower with upper limb, and lower limb(s) with rib(s) and sternum	Closed fracture of lower limb
Multiple closed fractures of skull AND/OR face with subarachnoid, subdural AND/OR extradural hemorrhage	Closed fracture of skull (disorder)
Multiple congenital anomalies of fetus	Multiple anomalies of fetus
Multiple congenital cerebral cysts	Multiple congenital cysts of brain (disorder)
Multiple congenital cerebral cysts	Multiple congenital cysts of cerebrum
Multiple defects of bilateral retinas without detachment	Multiple lesions of bilateral retinas without detachment (disorder)
Multiple defects of bilateral retinas without detachment	Bilateral multiple breaks of retina without detachment
Multiple defects of retina of left eye without detachment	Multiple lesions of retina of left eye without detachment (disorder)
Multiple defects of retina of left eye without detachment	Multiple breaks of retina of left eye without detachment
Multiple defects of retina of right eye without detachment	Multiple breaks of retina of right eye without detachment
Multiple defects of retina of right eye without detachment	Multiple lesions of retina of right eye without detachment (disorder)
Multiple defects of retina without detachment	Multiple breaks of retina without detachment (disorder)
Multiple defects of retina without detachment	Multiple lesions of retina without detachment (disorder)
Multiple dislocations	Dislocation of joint
Multiple dislocations	Dislocation of joint
Multiple endocrine adenomatosis (& [Wermer's syndrome])	Polyglandular activity in multiple endocrine adenomatosis
Multiple endocrine adenomatosis (& [Wermer's syndrome])	Multiple endocrine neoplasia, type 1 (disorder)
Multiple epiphyseal dysplasia tarda type IIIa	Multiple epiphyseal dysplasia due to collagen 9 anomaly is a rare primary bone dysplasia disorder characterized by normal or mild short stature, early-onset pain and/or stiffness of the joints (mainly affecting knees but also elbows, wrists, ankles and fingers, with relative sparing of the hips) and early degenerative joint disease. Other skeletal anomalies (including varus or valgus deformities, osteochondritis dissecans, abnormal carpal shape, free articular bodies) and mild myopathy have also been reported.
Multiple epiphyseal dysplasia tarda type IIIa	A very rare genetic necrotic bone disorder with clinical characteristics of painless swelling of the proximal interphalangeal joints associated with osteonecrosis of epiphyses followed by osteoarthritic changes, with onset before 25 years of age and often a benign course.
Multiple exostoses syndrome	Multiple congenital exostosis
Multiple exostoses syndrome	Disorder characterized by multiple exostoses (disorder)
Multiple exostosis syndromes	Multiple congenital exostosis
Multiple exostosis syndromes	Disorder characterized by multiple exostoses (disorder)
Multiple extreme injuries of abdominal organs	Injury of multiple intra-abdominal organs
Multiple fractures	Fractures involving multiple body regions
Multiple fractures involving both lower limbs, lower with upper limb, and lower limb(s) with rib(s) and sternum	Fracture of lower limb
Multiple fractures involving both upper limbs, and upper limb with rib(s) and sternum	Fracture of multiple ribs
Multiple fractures involving both upper limbs, and upper limb with rib(s) and sternum	Fractures involving multiple regions of both upper limbs
Multiple fractures involving both upper limbs, and upper limb with rib(s) and sternum	Fracture of sternum
Multiple fractures of both upper limbs	Fractures involving multiple regions of both upper limbs
Multiple fractures: [involving both upper limbs, and upper limb with rib(s) and sternum] or [arm] or [ribs] or [sternum]	Fractures involving multiple regions of both upper limbs
Multiple fractures: [involving both upper limbs, and upper limb with rib(s) and sternum] or [arm] or [ribs] or [sternum]	Fracture of multiple ribs
Multiple fractures: [involving both upper limbs, and upper limb with rib(s) and sternum] or [arm] or [ribs] or [sternum]	Fracture of sternum
Multiple fractures: [involving skull or face with other bones] or [multiple face fractures] or [multiple skull fractures]	Fracture of multiple bones of face (disorder)
Multiple fractures: [involving skull or face with other bones] or [multiple face fractures] or [multiple skull fractures]	Multiple fractures of skull
Multiple gated acquisition scanning	Multiple gated acquisition scanning (procedure)
Multiple gated acquisition scanning	Radionuclide blood pool study (procedure)
Multiple head and neck blood vessel injury	Injury of multiple blood vessels of head and/or neck (disorder)
Multiple injuries of ankle and/or foot	Multiple injuries of foot (disorder)
Multiple injuries of ankle and/or foot	Multiple injuries of ankle (disorder)
Multiple internal injuries	Multiple injuries (morphologic abnormality)
Multiple milia	Milia
Multiple mitral and aortic valve involvement	Diseases of mitral and aortic valves
Multiple myeloma and immunoproliferative disease	Immunoproliferative disorder
Multiple old intraocular nonmagnetic foreign bodies	Retained nonmagnetic foreign body in multiple sites of the eye
Multiple open fractures involving both lower limbs, lower with upper limb, and lower limb(s) with rib(s) and sternum	Open fracture of lower limb
Multiple open fractures of skull AND/OR face with cerebral laceration AND/OR contusion	Open fracture of skull with laceration of cerebrum (disorder)
Multiple open fractures of skull AND/OR face with cerebral laceration AND/OR contusion	Open fracture of skull with contusion of cerebrum
Multiple open fractures of skull AND/OR face with subarachnoid, subdural AND/OR extradural hemorrhage	Fracture of multiple bones of face (disorder)
Multiple open fractures of skull AND/OR face with subarachnoid, subdural AND/OR extradural hemorrhage	Multiple fractures of skull

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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)