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32570351000036105: Musculoskeletal finding reference set (foundation metadata concept)


Status: current, Primitive. Date: 31-May 2012. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id Description Lang Type Status Case? Module
108643301000036113 Musculoskeletal finding reference set en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension
108643311000036110 Musculoskeletal finding reference set (foundation metadata concept) en Fully specified name Active Case insensitive SNOMED Clinical Terms Australian extension
4351171000168112 <p>Supports the recording of musculoskeletal findings in Australian e-health implementations. This reference set has been derived from the <em>Clinical finding foundation reference set.</em></p><p>This reference set can be used:<ul><li>Within implementations where use-case specific reference sets for substances are yet to be developed.</li><li>As the basis for developing further use-case specific reference sets for substances, through a process of constraint.</li><li>As a benchmark, against which use-case specific reference sets that have been developed by the SNOMED CT-AU user community can be tested to assure that they are logical constraints of content relating to substances.</li></ul></p><p><b>Target client: </b>Australian e-health clinical information systems, for example, within Rheumatology groups.</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


14057 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Musculoskeletal finding reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 1766319133
Musculoskeletal finding reference set Developed by Australian Digital Health Agency true Inferred relationship Some 1779687638
Musculoskeletal finding reference set Is a Clinical finding foundation reference set false Inferred relationship Some
Musculoskeletal finding reference set Is a Rheumatology clinical group true Inferred relationship Some
Musculoskeletal finding reference set Is a Attribute value type false Inferred relationship Some
Musculoskeletal finding reference set Is a Simple type reference set true Inferred relationship Some

Members
Fractures involving multiple regions of upper limb(s) with lower limb(s)
Fractures involving thorax with lower back and pelvis
Fractures involving thorax with lower back and pelvis with limb(s)
Fractures of multiple bones of lower limb
Fragmented coronoid process
Francois syndrome
Frank-Ter Haar syndrome
Freeman-Sheldon syndrome
Frontal bossing
Frontal dysostosis
Frontal encephalocele
Fronto-frontal dysostosis
Fronto-malar faciosynostosis
Fronto-naso-ethmoidal dysostosis
Frontoethmoidal encephalocele
Gollop syndrome
Frontometaphyseal dysplasia
Frontonasal dysplasia sequence
Frontonasal dysplasia with alopecia and genital anomaly syndrome
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome
Frontorhiny
Fuhrmann syndrome
Fukuyama congenital muscular dystrophy
Full supernumerary rib
Full thickness rotator cuff tear
Fumbles with things
Fungal arthritis
Fungal musculoskeletal infection
Fungal myositis
GM1 gangliosidosis
Gait apraxia
Gait dyspraxia
Galeazzi fracture dislocation
Ganglion cyst of flexor tendon sheath of finger
Ganglion of tendon sheath
Ganglion cyst of tendon sheath of left hand
Ganglion cyst of tendon sheath of right hand
Ganglion of joint
Ganglion of multiple joints
Ganglion of superior tibiofibular joint
Gangrenous paraoesophageal hernia
Gap between cranial sutures
Gap in ribs
Gap in tendon
Gapping of tendon
Geleophysic dysplasia
Generalized arthritis
Generalised benign joint hypermobility
Generalised myasthenia
Generalised myokymia
Generalised neuromuscular exhaustion syndrome
Generalised osteoarthritis
Generalised osteoarthritis of the hand
Generally contracted pelvis with antenatal problem
Genetic recurrent myoglobinuria
Genetically determined myasthenia
Genochondromatosis
Genochondromatosis type 1
Genochondromatosis type 2
Genu recurvatum and long leg bone bowing
Geroderma osteodysplastica
Gestural apraxia
Diaphyseal dysplasia with anaemia
Giacci familial neurogenic acroosteolysis
Giant cell neoplasm of bone of pelvis
Giant cell neoplasm of clavicle
Giant cell neoplasm of long bone of lower limb
Giant cell neoplasm of mandible
Giant cell neoplasm of sacrum
Giant cell tumour of bone
Giant cell tumour of bone and articular cartilage
Giant cell tumour of craniofacial bones
Giant cell neoplasm of long bone of upper limb
Giant cell neoplasm of short bone of lower limb
Giant cell neoplasm of short bone of upper limb
Gingival and edentulous alveolar ridge lesion due to trauma
Glenoid labrum detachment
Glenoid labrum tear
Global developmental delay, osteopenia, ectodermal defect syndrome
Global instability of ankle
Glomus neoplasm of mastoid
Glossopalatine ankylosis
QRICH1-related intellectual disability, chondrodysplasia syndrome
Gluteal tendinitis
Glycogen storage disease due to lactate dehydrogenase deficiency
Glycogen storage disease due to muscle beta-enolase deficiency
Glycogen storage disease, muscular form
Glycogen storage disease type III
Glycogen storage disease, type IV
Glycogen storage disease, type V
Glycogen storage disease, type VII
Glycogen synthase deficiency
Gnathodiaphyseal dysplasia
Goldenhar syndrome
Gonarthrosis of left knee due to and following trauma
Gonarthrosis of right knee due to and following trauma
Gonococcal arthritis dermatitis syndrome
Gonococcal infection of joint
Gonococcal osteomyelitis
Gonococcal spondylitis

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