| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Morvan syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Action myoclonus renal failure syndrome |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Hypermanganesemia with dystonia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Hypermanganesemia with dystonia 2 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
5 |
| Hereditary essential tremor |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Dissociative neurological symptom disorder co-occurrent with dystonia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Sleep-related movement disorder caused by drug |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Sleep-related movement disorder caused by substance (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Transient motor tic (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Woodhouse Sakati syndrome |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
5 |
| Brain dopamine-serotonin vesicular transport disease (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Primary dystonia type 4 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Primary dystonia type 13 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Autosomal dominant focal dystonia DYT25 type (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Benign paroxysmal torticollis of infancy (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Developmental malformation, deafness, dystonia syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
5 |
| Huntington disease-like 2 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Dystonia 16 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Ataxia due to mitochondrial mutations |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Secondary tic disorder (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Tic due to developmental disorder (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Segmental myoclonus (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Primary tic disorder (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Sialidosis type 1 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Sensorineural hearing loss, early graying, essential tremor syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
5 |
| Paroxysmal exertion-induced dyskinesia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| McLeod neuroacanthocytosis syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Infant epilepsy with migrant focal crisis (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
1 |
| Hemidystonia hemiatrophy syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Infection causing tic (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
1 |
| Tic due to and following infection (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Chorea co-occurrent and due to Huntington disease-like condition (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Functional dystonia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Myoclonus, cerebellar ataxia, deafness syndrome |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
1 |
| Early-onset Lafora body disease (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
1 |
| Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Infantile convulsion and choreoathetosis syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Primary progressive freezing gait syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Autosomal dominant dopa responsive dystonia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Primary dystonia type 2 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Autosomal recessive dopa responsive dystonia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Primary dystonia 21 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Chronic hiccup (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Maternally inherited mitochondrial dystonia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Benign adult familial myoclonic epilepsy (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Hereditary geniospasm (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Insomnia co-occurrent and due to nocturnal myoclonus (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Dystonia of right hand (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Dystonia of left hand (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Shuddering attacks (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Sporadic olivopontocerebellar atrophy (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Focal dystonia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Dystonia of head (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Spasmodic torticollis as late effect of trauma (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Spasmodic torticollis due to infection |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Blepharospasm of right eyelid |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Blepharospasm of left eyelid |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Bilateral blepharospasm |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Primary dystonia DYT17 type (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Dystonia aphonia syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Tremor, nystagmus, duodenal ulcer syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
5 |
| Progressive myoclonic epilepsy type 5 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Progressive myoclonic epilepsy type 6 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Progressive myoclonic epilepsy type 3 |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Progressive myoclonic epilepsy type 8 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Cranio-cervical dystonia with laryngeal and upper limb involvement |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Adult-onset cervical dystonia DYT23 type (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Familial infantile myoclonic epilepsy |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Familial congenital mirror movements |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Huntington disease-like 1 (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Movement disorder due to toxicity of substance |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| dystonie orofaciale idiopathique |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Edentulous orofacial dystonia |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Refractory myoclonic epilepsy (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Idiopathic familial dystonia |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Primary torsion dystonia |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Movement disorder |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
1 |
| Apraxia as late effect of cerebrovascular disease |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| apraxie causée par un accident vasculaire cérébral |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Psychosis co-occurrent and due to Parkinson's disease (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Chorea due to and following encephalitis |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Ataxia due to disorder of immune function (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Cranial nerve palsy due to diabetes mellitus |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Cranial nerve palsy due to type 1 diabetes mellitus |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Cranial nerve palsy due to type 2 diabetes mellitus |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
4 |
| Childhood-onset basal ganglia degeneration syndrome |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Infantile-onset generalised dyskinesia with orofacial involvement |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Facial diplegia with paresthesia (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
5 |
| Tic disorder due to rheumatic chorea |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Tic disorder due to prion disease |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Tic disorder due to encephalitis (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Tic disorder due to neurosyphilis (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Hyperphenylalanineaemia due to DNAJC12 deficiency |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
2 |
| Tic disorder due to post-encephalitic syndrome |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Parkinsonism following Mycoplasma infection (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
| Parkinsonism due to prion disease (disorder) |
interprète (attribut) |
True |
Movement (observable entity) |
Inferred relationship |
Some |
3 |
FHIR