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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
Congenital kyphosis
Congenital kyphosis of cervicothoracic spine
Lack of ossification of auditory ossicles
Congenital laryngeal abductor palsy
Congenital laryngeal adductor palsy
Congenital laryngomalacia
Congenital laryngotracheo-oesophageal cleft
Congenital leg bone bowing
Congenital lethal myopathy Compton North type
CLOVES syndrome
Congenital lordosis and scoliosis deformity of spine
Congenital lordosis deformity of spine
Congenital lordosis deformity of spine due to congenital malformation of skeletal bone
Congenital lordosis/scoliosis
Congenital lumbar spondylolisthesis
Congenital lumbosacral fusion
Congenital lumbosacral spondylolisthesis
Congenital malformation of left calcaneus
Congenital malformation of right calcaneus
Congenital anomaly of sphenoid wing
Congenital malformation of sternum
Congenital mallet toe
Congenital malposition of arch of cervical vertebra
Congenital malposition of arch of lumbar vertebra
Congenital malposition of arch of sacral vertebra
Congenital malposition of arch of thoracic vertebra
Congenital malposition of calcaneus
Congenital malposition of carpal bone
Congenital malposition of cervical vertebra
Congenital malposition of femur
Congenital malposition of fibula
Congenital malposition of humerus
Congenital malposition of ilium
Congenital malposition of ischium
Congenital malposition of lumbar vertebra
Congenital malposition of metacarpal bone
Congenital malposition of metatarsal bone
Congenital malposition of pubis
Congenital malposition of radius
Congenital malposition of rib
Congenital malposition of sacral vertebra
Congenital malposition of sternebra
Congenital malposition of talus
Congenital malposition of tarsal bone
Congenital malposition of thoracic vertebra
Congenital malposition of tibia
Congenital malposition of ulna
Congenital mandibular asymmetry
Congenital mandibular hyperplasia
Congenital maxillary asymmetry
Congenital maxillary hyperplasia
Congenital maxillary hypoplasia
Congenital orbital meningocele
Congenital metatarsus valgus
Bilateral congenital metatarsus valgus
Congenital micrognathism
Congenital misalignment of arch of cervical vertebra
Congenital misalignment of arch of lumbar vertebra
Congenital misalignment of arch of sacral vertebra
Congenital misalignment of arch of thoracic vertebra
Congenital misalignment of centrum of cervical vertebra
Congenital misalignment of centrum of lumbar vertebra
Congenital misalignment of centrum of sacral vertebra
Congenital misalignment of centrum of thoracic vertebra
Congenital misalignment of pubis
Congenital misalignment of rib
Congenital misalignment of sternebra
Congenital monocular elevator palsy
Congenital multi-minicore disease with external ophthalmoplegia
Congenital myopathy Paradas type
Congenital muscular dystrophy due to LMNA mutation
Congenital muscular dystrophy type 1A
Congenital muscular dystrophy type 1B
Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation
Congenital muscular dystrophy type 1D large gene mutation
Congenital muscular dystrophy with arthrogryposis multiplex congenita
Congenital muscular dystrophy with cerebellar involvement
Congenital muscular dystrophy with hyperlaxity
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
Congenital muscular dystrophy with integrin alpha-7 deficiency
Congenital muscular dystrophy with intellectual disability
Congenital muscular dystrophy with intellectual disability and severe epilepsy
Congenital muscular dystrophy without intellectual disability
Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome
Congenital muscular hypertrophy-cerebral syndrome
Congenital myasthenic syndrome
Congenital myopathy with abnormal subcellular organelles
Congenital myopathy with fibre type disproportion
Congenital myopathy with internal nuclei and atypical cores
Congenital myopathy with myasthenic-like onset
Congenital myopathy with reduced type 2 muscle fibres
Congenital myopathy with uniform fibre type
Congenital myotonia, autosomal dominant form
Congenital myotonia, autosomal recessive form
Congenital myotonic dystrophy
Congenital negative ulnar variant of wrist
Congenital nonprogressive myopathy with Moebius and Robin sequences
Congenital osteodystrophy
Bilateral congenital overriding toes of feet
Congenital overriding toes of left foot
Congenital overriding toes of right foot

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