60342002: Movement disorder (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of movement\Movement disorder

\Disease\Movement disorder

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Movement disorder	Is a	Disorder of brain (disorder)	false	Inferred relationship	Some
Movement disorder	Is a	System disorder of the nervous system (disorder)	false	Inferred relationship	Some
Movement disorder	Finding site	Brain structure	false	Inferred relationship	Some
Movement disorder	Finding site	Structure of nervous system (body structure)	false	Inferred relationship	Some	1
Movement disorder	Is a	Finding of movement	true	Inferred relationship	Some
Movement disorder	Is a	Disease	true	Inferred relationship	Some
Movement disorder	Interprets	mouvement	false	Inferred relationship	Some	1
Movement disorder	Interprets	Movement observable	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Aspergillus clavatus tremors	Is a	True	Movement disorder	Inferred relationship	Some
Hypermobility syndrome (disorder)	Is a	True	Movement disorder	Inferred relationship	Some
A rare mitochondrial oxidative phosphorylation disorder characterized by myoclonic seizures, ataxia, generalized epilepsy, muscle weakness and ragged red fibers in the muscle biopsy.	Is a	True	Movement disorder	Inferred relationship	Some
A rare, genetic, neurological disorder characterized by childhood to adolescent onset of progressive myoclonus (which becomes very severe and results in major motor impediment) associated with infrequent tonic-clonic seizures, and, occasionally, ataxia. Learning disability prior to seizure onset and mild cognitive decline may be associated.	Is a	True	Movement disorder	Inferred relationship	Some
A rare, genetic, neurological disorder characterized by childhood-onset severe myoclonic and tonic-clonic seizures and early-onset ataxia leading to severe gait disturbances associated with normal to slightly diminished cognition. Scoliosis, diffuse muscle atrophy and subcutaneous fat loss, as well as developmental delay, may be associated. Brain MRI may reveal complete agenesis of the corpus callosum, ventriculomegaly, interhemispheric cysts, and simplified gyration (frontally).	Is a	True	Movement disorder	Inferred relationship	Some
A rare systemic disease characterized by generalized joint hypermobility with recurrent joint dislocations, redundant and hyperextensible skin with poor wound healing and abnormal scarring, easy bruising, and osteopenia/osteoporosis. Additional manifestations include hypotonia, delayed motor development, foot deformities, prominent superficial veins in the chest region, vascular complications (like mitral valve prolapse and aortic root dilation), hernias, dental anomalies, scoliosis, and facial dysmorphisms (like high palate, micrognathia, narrow palate). Mode of inheritance is autosomal recessive.	Is a	True	Movement disorder	Inferred relationship	Some
Impairment of motor nerve function as a complication of cutaneous surgery	Is a	True	Movement disorder	Inferred relationship	Some
Bobble-head doll syndrome	Is a	True	Movement disorder	Inferred relationship	Some
Dissociative neurological symptom disorder with tremor (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Autoimmune movement disorder	Is a	True	Movement disorder	Inferred relationship	Some
Chorea due to classical pantothenate kinase associated neurodegeneration (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to polycythemia rubra vera	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to paraneoplastic syndrome	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to hereditary ataxia (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to endocrine disorder	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to chronic hepatocerebral degeneration	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to anoxia of brain (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to and following ventriculoperitoneal shunt (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to prion disease (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to tardive dyskinesia	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to cerebral injury due to birth trauma (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to widespread metastatic malignant neoplastic disease (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to and following injury of head (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to immunological disorder (disorder)	Is a	False	Movement disorder	Inferred relationship	Some
Chorea due to metabolic disorder	Is a	False	Movement disorder	Inferred relationship	Some
Jumpy stump syndrome (disorder)	Is a	True	Movement disorder	Inferred relationship	Some
Andersen Tawil syndrome (disorder)	Is a	True	Movement disorder	Inferred relationship	Some
Dissociative motor disorder	Is a	False	Movement disorder	Inferred relationship	Some
A rare systemic disease characterized by the association of the features of Ehlers-Danlos syndrome with those of osteogenesis imperfecta. Predominant clinical manifestations include generalized joint hypermobility and dislocations, skin hyperextensibility and/or translucency, easy bruising, and invariable association with mild signs of osteogenesis imperfecta, including short stature, blue sclera, and osteopenia or fractures.	Is a	True	Movement disorder	Inferred relationship	Some
A rare primary bone dysplasia with multiple joint dislocations characterized by stunted stature, articular hypermobility and spinal malalignment resulting in severe progressive kyphosis. Joint dislocations include bilateral dislocation of the radial heads with elbow contractures, feet (bilateral talipes equinovarus) and congenital dislocations of the hip and genu valgus. Joint laxity is particularly observed in fingers. Spinal changes include moderate platyspondyly with anterior projection of the vertebral bodies. Facial features of oval face with a flattened nasal bridge, button nose, long upper lip, prominent eyes and blue sclera are characteristic but variable. Patients may also present mild skin extensibility, spatulate terminal phalanges, lip and palate clefts, micrognathia and structural cardiac malformations.	Is a	True	Movement disorder	Inferred relationship	Some
A rare primary bone dysplasia characterized by multiple joint dislocations, in particular in hips and knees present at birth, but the elbows, wrists, ankles, and patellae can also be affected; severe joint laxity, scoliosis, slender fingers with distal tapering, and growth deficiency developing in the post-natal period resulting in short stature. Gracile metacarpals and metatarsals, delayed bone age with poorly ossified carpal and tarsal bones, metaphyseal and epiphyseal dysplasia, slender ribs, and spondylar dysplasia are radiographical signs. Intelligence is usually normal.	Is a	True	Movement disorder	Inferred relationship	Some
Dissociative neurological disorder with symptom of movement disorder (disorder)	Is a	True	Movement disorder	Inferred relationship	Some
Astasia-abasia	Is a	True	Movement disorder	Inferred relationship	Some
Dysarthria-clumsy hand syndrome	Is a	True	Movement disorder	Inferred relationship	Some
Nerve palsy	Is a	True	Movement disorder	Inferred relationship	Some

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Reference Sets

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Id	Description	Lang	Type	Status	Case?	Module
100241018	Movement disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
799284018	Movement disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1850601000195116	disturbo del movimento	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
275911000077110	dyskinésie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
295191000172116	mouvement anormal	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
648271000172110	trouble du mouvement	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
405441000274111	Bewegungsstörung	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module