Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Choreoathetosis |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chorea due to inherited organic acidaemia |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to and following injury of head |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Chorea due to antiphospholipid syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to chronic hepatocerebral degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to endocrine disorder |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to hyperglycaemia |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to tardive dyskinesia |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to prion disease (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to Lesch-Nyhan syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to metabolic disorder |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to inherited aminoaciduria (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to anoxia of brain (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea caused by dopamine receptor antagonist (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to hereditary ataxia (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to and following ventriculoperitoneal shunt (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Chorea caused by oral contraceptive (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to cerebral injury due to birth trauma |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to ataxia telangiectasia syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to immunological disorder (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to neuroferritinopathy |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to polycythemia rubra vera |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to widespread metastatic malignant neoplastic disease (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to hypoparathyroidism (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to classical pantothenate kinase associated neurodegeneration (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to mitochondrial cytopathy |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to inborn error of metabolism (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to paraneoplastic syndrome |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea due to hyponatremia (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Choreoacanthocytosis |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dentatorubropallidoluysian degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Henoch's chorea |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Wilson's disease |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Pallidonigrospinal degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Rheumatic chorea with heart involvement |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Huntington's chorea |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Pallidonigral degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dubini's chorea |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pallidopontonigral degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Juvenile paralysis agitans of Hunt (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Birnbaum's syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Rheumatic chorea |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Pallidoluysian degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pigmentary pallidal degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Rheumatic chorea without heart involvement |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Juvenile onset Huntington's disease |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Late onset Huntington's disease (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Akinetic-rigid form of Huntington's disease |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Pallidal degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Benign hereditary chorea |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chorea due to systemic lupus erythematosus (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chorea due to thyrotoxicosis (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Kinesiogenic choreoathetosis |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chorea (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic chorea (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Paroxysmal nonkinesigenic dyskinesia (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Paroxysmal kinesigenic dyskinesia |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Huntington disease-like syndrome |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Huntington disease-like 3 |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Dissociative neurological symptom disorder co-occurrent with chorea |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia). |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Infection causing chorea |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chorea due to and following infective disorder (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Chorea co-occurrent and due to dentatorubropallidoluysian degeneration |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Infantile convulsion and choreoathetosis syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Acquired choreiform dyspraxia (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare genetic human prion disease characterised by adult-onset neurodegenerative manifestations associated with a movement disorder and psychiatric/behavioural disturbances. Patients typically present personality changes, aggressiveness, manias, anxiety and/or depression in conjunction with rapidly progressive cognitive decline (presenting with dysarthria, apraxia, aphasia and eventually leading to dementia) as well as ataxia (manifesting with gait disturbances, unsteadiness, coordination problems), Parkinsonism, myoclonus, and/or chorea. Additional features may include generalised spasticity, seizures, urine incontinence and pyramidal abnormalities. There is evidence the disease is caused by 8 extra octapeptide repeats in the PRNP gene on chromosome 20p13. |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chorea due to and following encephalitis |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Childhood-onset benign chorea with striatal involvement |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Classical pantothenate kinase associated neurodegeneration (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Atypical pantothenate kinase associated neurodegeneration (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Severe oculo-renal-cerebellar syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
13 |
Post-hemiplegic chorea |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acquired ataxia due to vitamin deficiency |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Andersen Tawil syndrome |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Astasia-abasia |
Interprets |
False |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dissociative paralysis (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dissociative astasia-abasia |
Interprets |
False |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dissociative motor disorder (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chorea due to injury of head (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chorea following injury (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Dystonia 28 (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Fisher's syndrome |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Dissociative neurological symptom disorder co-occurrent with facial spasm (disorder) |
Interprets |
False |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dissociative neurological disorder with symptom of movement disorder (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dissociative astasia-abasia |
Interprets |
False |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Astasia-abasia |
Interprets |
False |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Movement of eyelid |
Is a |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ataxic hemiparesis due to and following lacunar infarction (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Lacunar ataxic hemiparesis of right dominant side |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Lacunar ataxic hemiparesis of left dominant side |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Lacunar ataxic hemiparesis of left nondominant side |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Lacunar ataxic hemiparesis of right nondominant side |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Pure motor hemiparesis due to and following lacunar infarction (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Pure sensorimotor motor hemiparesis due to and following lacunar infarction (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Dysarthria-clumsy hand syndrome |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Facial palsy House-Brackmann grade V of right facial nerve (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Left facial palsy House-Brackmann grade V |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Facial palsy House-Brackmann grade VI of left facial nerve (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |