364564000: 'range of motion' van gewricht (waarneembare entiteit)

SNOMED CT Concept\Observable entity\...

\Process (observable entity)\Movement\Joint movement\Range of joint movement

\Clinical history/examination observable (observable entity)\Musculoskeletal observable\Joint observable\Joint movement\Range of joint movement

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Range of joint movement	Is a	Joint movement	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Lethal congenital contracture syndrome type 2 (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Lethal congenital contracture syndrome type 3 (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Foot joint - range of movement	Is a	True	Range of joint movement	Inferred relationship	Some
Hand joint range of movement (observable entity)	Is a	True	Range of joint movement	Inferred relationship	Some
Inherited arthrogryposis	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Malignant hyperthermia with arthrogryposis and torticollis syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	4
X-linked lethal multiple pterygium syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Lethal congenital contracture syndrome type 5	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	7
Neurogenic arthrogryposis multiplex congenita (disorder)	Interprets	False	Range of joint movement	Inferred relationship	Some	2
Autosomal dominant multiple pterygium syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Distal arthrogryposis type 5D (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	5
Larsen-like syndrome B3GAT3 type	Interprets	True	Range of joint movement	Inferred relationship	Some	4
congenitale neuropathie met arthrogryposis multiplex congenita	Interprets	False	Range of joint movement	Inferred relationship	Some	3
Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Camptobrachydactyly (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	4
Autism spectrum disorder, epilepsy, arthrogryposis syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Contracture of joint	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Distal arthrogryposis type 1 (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Neurogenic arthrogryposis multiplex congenita (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	4
On examination - reduced joint movement	Interprets	False	Range of joint movement	Inferred relationship	Some	4
On examination - reduced movement of spine	Interprets	False	Range of joint movement	Inferred relationship	Some	2
On examination - reduced movement of arm	Interprets	False	Range of joint movement	Inferred relationship	Some	2
Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	4
Contracture of multiple joints	Interprets	True	Range of joint movement	Inferred relationship	Some	2
German syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	1
Contracture of joint following injury (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Lethal congenital contracture syndrome type 1 (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Congenital arthrogryposis caused by teratogen (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
On examination - reduced movement of wrist	Interprets	False	Range of joint movement	Inferred relationship	Some	2
Hydrocephalus with cleft palate and joint contracture syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	9
Distal arthrogryposis syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Temporomandibular joint stiff	Interprets	False	Range of joint movement	Inferred relationship	Some	1
Arthrogryposis and ectodermal dysplasia syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	6
Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder)	Interprets	False	Range of joint movement	Inferred relationship	Some	4
Kuskokwim syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Congenital contractural arachnodactyly	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Multiple stiff joints	Interprets	True	Range of joint movement	Inferred relationship	Some	1
Morning stiffness - joint	Interprets	True	Range of joint movement	Inferred relationship	Some	1
Marfanoid joint hypermobility syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Hypermobility of joint	Interprets	True	Range of joint movement	Inferred relationship	Some	1
spondylo-epimetafysaire dysplasie met gewrichtslaxiteit	Interprets	False	Range of joint movement	Inferred relationship	Some	4
Distal arthrogryposis type 3 (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	4
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	4
NEK9-related lethal skeletal dysplasia	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Joint contractures, developmental delay, Pierre Robin syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	5
Spondyloepiphyseal dysplasia Stanescu type	Interprets	True	Range of joint movement	Inferred relationship	Some	4
Arthrofibrosis	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	4
Hypermobility syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Hypermobile Ehlers-Danlos syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	5
Generalized benign joint hypermobility	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Localised benign joint hypermobility	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Myopathic Ehlers-Danlos syndrome (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	6
Classical-like Ehlers-Danlos syndrome type 2	Interprets	True	Range of joint movement	Inferred relationship	Some	6
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Antenatal multi-minicore disease with arthrogryposis multiplex congenita	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Diastrophic dysplasia	Interprets	True	Range of joint movement	Inferred relationship	Some	4
Arthrogryposis multiplex congenita	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Pena-Shokeir syndrome type I (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Marden Walker syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Microphthalmia, microtia, fetal akinesia syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	7
Hecht syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Congenital muscular dystrophy with arthrogryposis multiplex congenita	Interprets	True	Range of joint movement	Inferred relationship	Some	3
Congenital amyoplasia (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2
Ehlers-Danlos and osteogenesis imperfecta syndrome	Interprets	True	Range of joint movement	Inferred relationship	Some	7
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type	Interprets	True	Range of joint movement	Inferred relationship	Some	4
Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	5
Congenital pontocerebellar hypoplasia type 12	Interprets	True	Range of joint movement	Inferred relationship	Some	7
Contracture of temporomandibular joint (disorder)	Interprets	True	Range of joint movement	Inferred relationship	Some	2

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Id	Description	Lang	Type	Status	Case?	Module
487722017	Range of joint movement	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
770826013	Range of joint movement (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2164870013	Range of motion	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
12302371000146114	‘range of motion’ van gewricht	nl	Synonym (core metadata concept)	Inactive	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12302381000146111	‘range of motion’ van gewricht (waarneembare entiteit)	nl	Fully specified name	Inactive	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12302391000146113	bewegingsbereik van gewricht	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12302401000146111	ROM van gewricht	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12302411000146113	bewegingsuitslag van gewricht	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
13342081000146114	'range of motion' van gewricht (waarneembare entiteit)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
13342091000146111	'range of motion' van gewricht	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)