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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
Aseptic necrosis of talus
Aseptic necrosis of vertebral body
Aspartylglucosaminuria
Assimilation pelvis
Astley-Kendall dysplasia
Astragaloscaphoid synostosis
Astronaut-bone demineralisation syndrome
Asymmetric crying face association
Asymmetrical arthritis
Asymmetrical genu valgum
Asymmetrical skull
Asymmetry of inferior border of mandible
Asymmetry of jaw
Asymmetry of mandible
Asymmetry of maxilla
Asymmetry of pelvis
Asymptomatic calcium pyrophosphate deposition disease
Asynergia
Atelosteogenesis
Atelosteogenesis type 1
Atelosteogenesis type 2
Atelosteogenesis type 3
Atlanto-occipital ankylosis
Atlanto-occipital joint sprain
Atlanto-occipital malformation
Atlantoaxial ankylosis
Atlantoaxial instability
Atlantoaxial joint sprain
Atrophic nonunion of fracture
Atrophy of deltoid muscle
Atrophy of edentulous alveolar ridge
Atrophy of edentulous mandibular alveolar ridge
Atrophy of edentulous maxillary alveolar ridge
Atrophy of gastrocnemius muscle
Atrophy of gluteus maximus muscle
Atrophy of interosseous muscle of hand
Atrophy of latissimus dorsi muscle
Bilateral muscle atrophy of ankles
Muscle atrophy of left ankle
Muscle atrophy of right ankle
Bilateral muscle atrophy of feet
Bilateral atrophy of muscle of forearms
Bilateral atrophy of muscle of lower legs
Bilateral muscle atrophy of shoulders
Bilateral atrophy of muscle of thighs
Bilateral atrophy of muscle of upper arms
Atrophy of muscle of left foot
Atrophy of muscle of left forearm
Atrophy of muscle of left hand
Atrophy of muscle of left lower leg
Atrophy of muscle of left shoulder
Atrophy of muscle of left thigh
Atrophy of muscle of left upper arm
Atrophy of muscle of right foot
Atrophy of muscle of right forearm
Atrophy of muscle of right hand
Atrophy of muscle of right lower leg
Atrophy of muscle of right shoulder
Atrophy of muscle of right thigh
Atrophy of muscle of right upper arm
Atrophy of pectoral muscle
Atrophy of quadriceps femoris muscle
Atrophy of skeletal muscle of pelvis
Atrophy of temporalis muscle
Atrophy of trapezius muscle
Atypical appearance of mandibular condyle
Atypical condylar angulation of mandible
Atypical fracture of femur
Atypical hypotonia cystinuria syndrome
Audible joint crepitus
Auriculo-condylar syndrome
Autoimmune inflammation of skeletal muscle
Autoimmune interstitial lung disease, arthritis syndrome
Autoimmune myopathy
Autoimmune necrotising myopathy
Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant Robinow syndrome
Autosomal dominant brachyolmia
Autosomal dominant central core disease
Autosomal dominant centronuclear myopathy
Autosomal dominant congenital fibre-type disproportion myopathy due to ACTA1 mutation
Autosomal dominant congenital fibre-type disproportion myopathy due to SELENON mutation
Autosomal dominant congenital fibre-type disproportion myopathy due to TPM3 mutation
Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome
Autosomal dominant hypophosphataemic bone disease
Autosomal dominant hypophosphataemic rickets
Autosomal dominant limb girdle muscular dystrophy type 1A
Autosomal dominant limb girdle muscular dystrophy type 1D
Autosomal dominant limb girdle muscular dystrophy type 1E
Autosomal dominant limb girdle muscular dystrophy type 1F
Autosomal dominant limb girdle muscular dystrophy type 1G
Autosomal dominant limb-girdle muscular dystrophy type 1H
Autosomal dominant mitochondrial myopathy with exercise intolerance
Autosomal dominant muscular dystrophy not predominantly limb girdle
Autosomal dominant muscular dystrophy with gene located at 5q31
Autosomal dominant muscular dystrophy with limb girdle distribution
Autosomal dominant myoglobinuria
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
Autosomal dominant omodysplasia
Autosomal dominant osteopetrosis type 2

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