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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
Heat cramp
Heberden's node
Bilateral Heberden nodes
Heberden node of the distal interphalangeal joints of the left hand
Heberden node of the distal interphalangeal joints of the right hand
Hedblom's syndrome
Heel DXA scan result normal
Heel dual energy X-ray photon absorptiometry scan result osteopenic
Heel DXA scan result osteoporotic
Haemangioma of bone
Haemangioma of vertebral column
Haemarthrosis
Haemarthrosis of acromioclavicular joint
Bilateral haemarthrosis of knee joints
Haemarthrosis of distal interphalangeal joint of finger
Haemarthrosis of distal radioulnar joint
Haemarthrosis of elbow
Haemarthrosis-1st metatarsophalangeal joint
Haemarthrosis of glenohumeral joint
Haemarthrosis of hand
Haemarthrosis of hip
Haemarthrosis of interphalangeal joint of toe
Haemarthrosis of knee
Haemarthrosis of left knee
Haemarthrosis of lesser metatarsophalangeal joint
Haemarthrosis of MCP joint
Haemarthrosis of multiple sites
Haemarthrosis of proximal interphalangeal joint of finger
Haemarthrosis of right knee
Haemarthrosis of sacroiliac joint
Haemarthrosis of shoulder region
Haemarthrosis of sternoclavicular joint
Haemarthrosis of subtalar joint
Haemarthrosis of talonavicular joint
Haemarthrosis of the ankle
Haemarthrosis of the ankle and/or foot
Haemarthrosis of tibiofibular joint
Haemarthrosis of wrist
Haematoma of rectus sheath
Hemifacial microsomia
Oculoauriculovertebral spectrum with radial defects
Hemihypertrophy of muscle
Hemimaxillofacial dysplasia
Hemimyelocele
Hemithorax immobile
Haemophilic arthropathy
Haemorrhage of muscle
Glycogen storage disease due to hepatic glycogen synthase deficiency
Hepatic osteodystrophy
Hereditary acroosteolysis
Hereditary arterial and articular multiple calcification syndrome
Hereditary camptodactyly
Hereditary continuous muscle fibre activity
Hereditary disorder of musculoskeletal system
Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome
Hereditary hypophosphataemic rickets with hypercalciuria
Hereditary inclusion body myopathy type 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome
Hereditary myopathy associated with hydrocephalus
Hereditary myopathy limited to females
Hereditary proximal myopathy with early respiratory failure
Hereditary progressive muscular dystrophy
Hernia of muscle through fascia of lower leg
Herniation of lumbar muscles
Herniation of nucleus pulposus
Heterotopic ossification of joint
Heterotopic ossification of tendon
Hiatal hernia
Hiatal hernia with gangrene AND obstruction
Gastro-oesophageal reflux disease with hiatal hernia
Hiatus hernia with gangrene
Hiatus hernia with obstruction
Hiccups
High assimilation pelvis
High bone mass osteogenesis imperfecta
High frequency muscle fatigue
High lumbar myelomeningocele
High orbit
Hill-Sachs lesion
Hip DXA scan result osteoporotic
Hip DXA scan result normal
Hip DXA scan result osteopenic
Hip dysplasia Beukes type
Upington disease
Hip held in external rotation
Hip joint crepitus
Hip joint crepitus audible
Hip joint crepitus palpable
Hip joint deformity in external rotation
Hip joint effusion
Hip joint fixed flexion deformity
Hip joint hypermobility
Hip joint inflamed
Hip joint laxity
Hip joint painful on movement
Hip joint prosthesis present
Hip joint stable
Hip joint swollen
Hip joint valgus deformity
Hip juvenile osteochondropathy
Hip pain

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