FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.9.0  |  FHIR Version n/a  User: [n/a]

900000000000523009: POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT model component

Descriptions:

Id Description Lang Type Status Case? Module
900000000001150016 POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept) en Fully specified name Active Case sensitive SNOMED CT model component
900000000001151017 POSSIBLY EQUIVALENT TO association reference set en Synonym Active Case sensitive SNOMED CT model component

49301 members. Search Members:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
POSSIBLY EQUIVALENT TO association reference set Is a Historical association true Inferred relationship Some
Members associationTargetComponent
Audiometry Audiogram
Audiometry Audiogram
Audiometry Auditory function test
Audiometry Auditory function test
Audiometry Auditory acuity evaluation
Audiometry Auditory acuity evaluation
Audiometry Hearing examination
Audiometry Auditory acuity evaluation
Audiometry Hearing examination
Audiometry Auditory function test
Audiometry Audiometric test
Audiometry Audiometric test
Audiometry Hearing examination
Audiometry Audiogram
Audiometry Audiometric test
Auditory &/or vestibular testing Vestibular function test
Auditory &/or vestibular testing Hearing examination
Auditory &/or vestibular testing Vestibular function test
Auditory &/or vestibular testing Hearing examination
Auditory area (sound intensity) Auditory area
Auditory canal structure External auditory canal structure
Auditory function test Hearing examination
Auditory function test Auditory function test
Auditory function test Audiogram
Auditory function test Audiometric test
Auditory function test Auditory acuity evaluation
Auditory pathway structure Structure of auditory system
Auditory pathway structure Structure of central auditory system
Auditory pathway structure Structure of auditory system
Auditory pathway structure Structure of central auditory system
Auditory pathway structure Acoustic radiations structure
Auditory/vestibular test NOS Vestibular function test
Auditory/vestibular test NOS Vestibular function test
Auditory/vestibular test NOS Hearing examination
Auditory/vestibular test NOS Hearing examination
Auditory/vestibular test abnormal (& [audiogram]) Audiogram abnormal
Auditory/vestibular test abnormal (& [audiogram]) Auditory/vestibular test abnormal
Auditory/vestibular test abnormal (& [audiogram]) Auditory/vestibular test abnormal
Auditory/vestibular test abnormal (& [audiogram]) Audiogram abnormal
Auditory/vestibular test normal (& [hearing] or [audiogram]) Audiogram normal
Auditory/vestibular test normal (& [hearing] or [audiogram]) Auditory/vestibular test normal
Auditory/vestibular test normal (& [hearing] or [audiogram]) Hearing test normal
Auditory/vestibular test normal (& [hearing] or [audiogram]) Auditory/vestibular test normal
Auditory/vestibular test normal (& [hearing] or [audiogram]) Hearing test normal
Auditory/vestibular test normal (& [hearing] or [audiogram]) Audiogram normal
Augmentation - action Surgical augmentation - action
Aurantimonas species Aurantimonas species
Auscultation - action Auscultation - action
Auscultation - action Auscultation
Australian echidna Tachyglossus aculeatus
Australian echidna Family Tachyglossidae
Australian pine pollen allergen Australian pine pollen
Australian thick-knee Burhinus giganteus
Australian thick-knee Burhinus grallarius
Autistic disorder Infantile psychosis
Autistic disorder Autistic disorder
Autistic disorder Infantile autism
Autoaugmentation of bladder Clam cystoplasty
Autoaugmentation of bladder Autoaugmentation of bladder
Autogenous skin free graft Full thickness autograft of skin
Autogenous skin free graft Split thickness skin graft
Autogenous vaccine - autogenous bacterin Vaccine product
Autoimmune haemolytic anaemia Haemolytic disease of fetus OR newborn due to isoimmunisation
Autoimmune haemolytic anaemia Autoimmune haemolytic anaemia
Autoimmune haemolytic anaemia Haemolytic disease of fetus OR newborn due to isoimmunisation
Autoimmune haemolytic anaemia Autoimmune haemolytic anaemia
Autoimmune progesterone dermatitis/urticaria Menstrual urticaria
Autoimmune progesterone dermatitis/urticaria Autoimmune progesterone dermatitis
Autologous 12million chondrocyte cells injection solution vial for implantation Autologous cultured chondrocyte 30 million unit/mL conventional release intraarticular implant
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
Automatic pneumatic pulmonary resuscitator, single-use Automatic pulmonary resuscitator
Autonomic nervous system disorder: [NOS] or [Horner's] or [failure] Horner's syndrome pupil
Autonomic nervous system disorder: [NOS] or [Horner's] or [failure] Pure autonomic failure
Autonomic nervous system poisoning NOS Drug toxicity
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
Autosomal dominant analbuminaemia Congenital analbuminaemia
Autosomal dominant epidermolysis bullosa simplex Autosomal dominant epidermolysis bullosa simplex
Autosomal dominant epidermolysis bullosa simplex Epidermolysis bullosa simplex, Ogna type
Autosomal dominant isolated somatotropin deficiency Autosomal dominant isolated somatotropin deficiency
Autosomal dominant isolated somatotropin deficiency Ateliotic dwarfism without insulinopenia
Autosomal recessive muscular dystrophy with gene located at 15q Autosomal recessive limb girdle muscular dystrophy type 2A
Hereditary sensory and autonomic neuropathy, type II Charcot-Marie-Tooth disease, type II
Hereditary sensory and autonomic neuropathy, type II Hereditary sensory and autonomic neuropathy type II
Hereditary sensory and autonomic neuropathy, type II Hereditary insensitivity to pain with anhidrosis
Autosomal recessive spondyloepimetaphyseal dysplasia Spondyloepimetaphyseal dysplasia Irapa type
Autotransplantation of pancreatic tissue Reimplantation of pancreatic tissue
Autotransplantation of pancreatic tissue Autotransplant of pancreatic tissue
Avascular necrosis of bone Aseptic necrosis of bone
Avascular necrosis of bone Aseptic necrosis
Avascular necrosis of bone Avascular necrosis of bone
Avascular necrosis of femoral condyle (& [medial]) Avascular necrosis of the medial femoral condyle
Avian adeno-associated virus Muscovy duck parvovirus
Avian adeno-associated virus Goose parvovirus
Avian adenovirus 2 antibody Turkey adenovirus 3 antibody
Avian adenovirus 2 antibody assay Measurement of Turkey adenovirus 3 antibody

Start Previous Page 81 of 494 Next End

Reference Sets

Reference set descriptor

Back to Start