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
Auditory/vestibular test NOS	Vestibular function test
Auditory/vestibular test abnormal (& [audiogram])	Audiogram abnormal
Auditory/vestibular test abnormal (& [audiogram])	Auditory/vestibular test abnormal (finding)
Auditory/vestibular test abnormal (& [audiogram])	Auditory/vestibular test abnormal (finding)
Auditory/vestibular test abnormal (& [audiogram])	Audiogram abnormal
Auditory/vestibular test normal (& [hearing] or [audiogram])	Auditory/vestibular test normal (finding)
Auditory/vestibular test normal (& [hearing] or [audiogram])	Hearing test normal
Auditory/vestibular test normal (& [hearing] or [audiogram])	Audiogram normal
Auditory/vestibular test normal (& [hearing] or [audiogram])	Audiogram normal
Auditory/vestibular test normal (& [hearing] or [audiogram])	Hearing test normal
Auditory/vestibular test normal (& [hearing] or [audiogram])	Auditory/vestibular test normal (finding)
Augmentation - action	Surgical augmentation - action
Augmentation genioplasty with graft and implant	Augmentation of chin using sliding osteotomy and interpositional autograft (procedure)
Augmentation genioplasty with graft and implant	Augmentation of chin using implant (procedure)
Aurantimonas species	Genus Aurantimonas (organism)
Auscultation - action	Auscultation - action (qualifier value)
Auscultation - action	A listening to spontaneously generated body sounds
Australian echidna	Tachyglossus aculeatus (organism)
Australian echidna	Family Tachyglossidae (organism)
Australian pine pollen allergen	Australian pine pollen
Australian thick-knee	Burhinus giganteus (organism)
Australian thick-knee	Burhinus grallarius (organism)
Autoaugmentation of bladder	Clam cystoplasty
Autoaugmentation of bladder	Autoaugmentation of urinary bladder
Autogenous skin free graft	Split thickness graft of skin to skin (procedure)
Autogenous skin free graft	Full thickness autograft of skin (substance)
Autogenous vaccine - autogenous bacterin	Vaccine product
Autoimmune haemolytic anaemia	Hemolytic disease of fetus OR newborn due to isoimmunization (disorder)
Autoimmune haemolytic anaemia	Autoimmune hemolytic anemia (disorder)
Autoimmune hemolytic anemia	Autoimmune hemolytic anemia (disorder)
Autoimmune hemolytic anemia	Hemolytic disease of fetus OR newborn due to isoimmunization (disorder)
Autoimmune progesterone dermatitis/urticaria	Autoimmune progesterone dermatitis
Autoimmune progesterone dermatitis/urticaria	Menstrual urticaria
Autologous 12million chondrocyte cells injection solution vial for implantation	Product containing precisely autologous cultured chondrocyte 30 million unit/1 milliliter conventional release intraarticular implant (clinical drug)
Automatic cranial perforator, reusable	Automatic-releasing cranial perforator
Automatic cranial perforator, single-use	Automatic-releasing cranial perforator
Automatic pneumatic pulmonary resuscitator, reusable	Automatic pulmonary resuscitator (physical object)
Automatic pneumatic pulmonary resuscitator, single-use	Automatic pulmonary resuscitator (physical object)
Autonomic nervous system poisoning NOS	Poisoning caused by drug AND/OR medicinal substance (disorder)
Autopen 1.5mL one unit device	Injection device
Autopen 1.5mL two unit device	Injection device
Autopen 3mL two unit device	Injection device
Autopen device	Injection device
Autopsied body	Autopsied body (finding)
Autosomal dominant analbuminemia	Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA).
Autosomal dominant epidermolysis bullosa simplex	Autosomal dominant epidermolysis bullosa simplex (disorder)
Autosomal dominant epidermolysis bullosa simplex	Epidermolysis bullosa simplex, Ogna type (disorder)
Autosomal dominant familial isolated hypoparathyroidism	Autosomal dominant hypocalcemia (disorder)
Autosomal dominant familial isolated hypoparathyroidism	Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder)
Autosomal dominant familial isolated hypoparathyroidism	Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder)
Autosomal dominant familial isolated hypoparathyroidism	A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects.
Autosomal dominant isolated somatotropin deficiency	Ateliotic dwarfism without insulinopenia
Autosomal dominant isolated somatotropin deficiency	Autosomal dominant isolated somatotropin deficiency
Autosomal recessive familial isolated hypoparathyroidism	Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder)
Autosomal recessive familial isolated hypoparathyroidism	A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects.
Autosomal recessive familial isolated hypoparathyroidism	Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder)
Autosomal recessive muscular dystrophy with gene located at 15q	A subtype of autosomal recessive limb girdle muscular dystrophy characterized by a variable age of onset of progressive, typically symmetrical and selective weakness and atrophy of proximal shoulder- and pelvic-girdle muscles (gluteus maximus, thigh adductors, and muscles of the posterior compartment of the limbs are most commonly affected) without cardiac or facial involvement. Clinical manifestations include exercise intolerance, a waddling gait, scapular winging and calf pseudo-hypertrophy.
Hereditary sensory and autonomic neuropathy, type II	Hereditary insensitivity to pain with anhidrosis (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)
Autosomal recessive spondyloepimetaphyseal dysplasia	Spondyloepimetaphyseal dysplasia, Irapa type is characterized by disproportionate short-trunked short stature, pectus carinatum, short arms, short and broad hands, short metatarsals, flat and broad feet, coxa vara, genu valgum, osteoarthritis, arthrosis and moderate-to-serious gait impairment.
Avascular necrosis of femoral condyle (& [medial])	Avascular necrosis of medial femoral condyle (disorder)
Avian adeno-associated virus	Muscovy duck parvovirus (organism)
Avian adeno-associated virus	Goose parvovirus (organism)
Avian adenovirus 2 antibody	Turkey adenovirus 3 antibody
Avian adenovirus 2 antibody assay	Measurement of Turkey adenovirus 3 antibody (procedure)
Avian herpesvirus	Gallid herpesvirus 2 (organism)
Avian herpesvirus	Anatid herpesvirus 1 (organism)
Avian herpesvirus	Gallid herpesvirus 3 (organism)
Avian herpesvirus	Gallid herpesvirus 1 (organism)
Avian infectious bronchitis virus Ark-99	Antibody to Avian infectious bronchitis virus Ark-99 (substance)
Avian influenza	Influenza caused by Influenza A virus (disorder)
Avian influenza virus, highly pathogenic	Influenza A virus (organism)
Avian influenza virus, low pathogenic	Influenza A virus (organism)
Avian parvovirus	Muscovy duck parvovirus (organism)
Avian parvovirus	Chicken parvovirus (organism)
Avian parvovirus	Goose parvovirus (organism)
Avian reticuloendotheliosis virus	Reticuloendotheliosis virus (organism)
Avian reticuloendotheliosis virus	Reticuloendotheliosis virus (strain T,A) (organism)
Avian sarcoma virus	Avian sarcoma virus (organism)
Avian sarcoma virus	Rous sarcoma virus (organism)
Avian type C oncovirus group	Genus Alpharetrovirus (organism)
Avian type C oncovirus group	Reticuloendotheliosis virus (organism)
Avibactam and ceftazidime	Product containing avibactam and ceftazidime (medicinal product)
Avioserpens species	Avioserpens (organism)
Avocet	Genus Recurvirostra (organism)
Avulsion leg varicose vein (& Babcock)	Avulsion of varicose vein of leg
Avulsion of eye	Traumatic enucleation of eye
Axenfeld's anomaly	Posterior embryotoxon (disorder)
Axenfeld's anomaly	Axenfeld anomaly
Axilla	Axillary region structure
Axilla	Entire axillary region
Axilla	Structure of axillary fossa (body structure)
Axilla	Entire axillary fossa
Axilla	Axillary region structure
Axilla	Entire axillary fossa
Axilla	Structure of axillary fossa (body structure)
Axilla	Entire axillary region
Axilla structure	Axillary region structure
Axilla structure	Structure of axillary fossa (body structure)
Axillary artery and its branches	Entire axillary artery

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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)