Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Mirror movements |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Oral dyskinesia |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Painful legs and moving toes |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Myoclonic disorder |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Restless legs |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Grimaces |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Benedikt's syndrome (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Medication-induced movement disorder |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare neurological disorder comprising fluctuating trunk and limb stiffness, painful muscle spasms, task-specific phobia related to walking, an exaggerated startle response, and often ankylosing deformities such as fixed lumbar hyperlordosis. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Tic disorder |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paradoxical facial movements |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Extrapyramidal disease |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Dubini's chorea |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Tic of organic origin |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
On examination - associated movements |
Associated finding |
False |
Movement disorder |
Inferred relationship |
Some |
|
White shaker dog syndrome |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Ballism (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Apraxia due to cerebrovascular accident (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Family history of movement disorder (situation) |
Associated finding |
False |
Movement disorder |
Inferred relationship |
Some |
1 |
Family history of movement disorder (situation) |
Associated finding |
True |
Movement disorder |
Inferred relationship |
Some |
1 |
Family history of movement disorder (situation) |
Associated finding |
False |
Movement disorder |
Inferred relationship |
Some |
1 |
Shuddering attacks (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Organic sleep related movement disorder (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Essential tremor |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Deafness-dystonia-optic neuronopathy syndrome (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Frontotemporal dementia with parkinsonism-17 |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Primary progressive freezing gait syndrome (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare tremor disorder characterized by an isolated high frequency (>12Hz) tremor that occurs when standing, typically in weight-bearing muscles, causing a feeling of unsteadiness or discomfort, which disappears when not standing. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Chronic hiccup is a rare movement disorder characterized by involuntary spasmodic contractions of the inspiratory muscles synchronized with larynx closure lasting for more than 48 hours. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare genetic tremor disorder characterized by recurrent episodes of involuntary tremor of the chin and lower lip due to isolated myoclonus of the mentalis muscle. Patients may represent more severe symptoms such as tongue biting and psychological distress. Even though neurological abnormalities are not associated, occasional involvement of sleep disorders and other facial muscles have been described. Sporadic cases were also reported. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Ataxia due to mitochondrial mutations |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Acquired ataxia |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Tremor due to metabolic disorder |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Tremor due to harmful pattern of substance use |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Movement disorder due to toxicity of substance |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Benign paroxysmal tonic upgaze of childhood with ataxia is a rare paroxysmal movement disorder characterized by episodes of sustained, conjugate, upward deviation of the eyes and down beating saccades in attempted downgaze (with preserved horizontal eye movements) which is accompanied by ataxic symptomatology (unsteady gait, lack of balance and movement coordination disturbances) in an otherwise healthy individual. Bilateral vertical nystagmus is associated. Symptoms generally disappear spontaneously within 1-2 years after onset. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Familial dyskinesia and facial myokymia is a rare paroxysmal movement disorder, with childhood or adolescent onset, characterized by paroxysmal choreiform, dystonic, and myoclonic movements involving the limbs (mostly distal upper limbs), neck and/or face, which can progressively increase in both frequency and severity until they become nearly constant. Patients may also present with delayed motor milestones, perioral and periorbital dyskinesias, dysarthria, hypotonia, and weakness. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare, X-linked, syndromic intellectual disability disease characterized by neonatal hypertonia which evolves to hypotonia and an exaggerated startle response (to sudden visual, auditory or tactile stimuli), followed by the development of early-onset, frequently refractory, tonic or myoclonic seizures. Progressive epileptic encephalopathy, intellectual disability, and psychomotor development arrest, with subsequent decline, may be additionally associated. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare, genetic, syndromic intellectual disability disease characterized by global developmental delay, microcephaly, mild to moderate intellectual disability, truncal ataxia, trunk and limb, or generalized, choreiform movements, and elevated serum creatine kinase levels. Variably associated features include mild cerebral atrophy, muscular weakness or hypotonia in early childhood, and/or seizures. Ocular abnormalities (e.g. exophoria, anisometropia, amblyopia) have been reported. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
The occurrence of abnormal involuntary movements that are incongruent with a known neurologic cause and are significantly improved on neurological exam with distraction or non-physiologic maneuvers. The disorder is defined by its clinical appearance, rather than by any causative speculation. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Tremor due to pheochromocytoma |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Chorea due to heredodegenerative disorder |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Infection causing chorea (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Chorea due to and following infective disorder (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Tongue protrusion disorder of twelfth cranial nerve |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Marfanoid joint hypermobility syndrome |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Contracture of joint |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Tongue deviation disorder of twelfth cranial nerve |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Tourniquet palsy |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Congenital laryngeal abductor palsy |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Congenital laryngeal adductor palsy (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Multiple pterygium syndrome |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Clumsiness - motor delay |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Periodic limb movement disorder (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Vagus nerve laryngeal paralysis |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Tick paralysis |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare genetic neuromuscular channelopathy characterized by normokalemic episodes of painful muscle cramping followed by progressive, permanent, flaccid weakness, triggered by stress, cold and exercise, associated with myopathic myopathy and painful acute edema with neuronal compression, foot drop and muscle degeneration when located in the tibialis anterior muscle group. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Periodic paralysis with later-onset distal motor neuropathy is a rare, genetic, neuromuscular disease characterized by acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset, chronic, slowly progressive, distal, axonal neuropathy. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Muscle paralysis due to and following neuromuscular blockade (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A general term used to refer to any damage to or abnormality of the joint structure or surrounding soft tissue resulting in a limitation of joint movement. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Dissociative neurological symptom disorder co-occurrent with chorea |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Dissociative neurological symptom disorder co-occurrent with myoclonus (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
trouble neurologique dissociatif symptomatique concomitant de tremblement |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Diabetic hand syndrome |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
dysplasie spondylo-épimétaphysaire avec hyperlaxité ligamentaire |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Pharyngeal paralysis |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paralysis of larynx |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Facial palsy (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Chorea co-occurrent and due to systemic lupus erythematosus |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Functional chorea |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Neck pain co-occurrent with neck stiffness following whiplash injury to neck (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Flaccid monoplegia of upper limb (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Flaccid monoplegia of lower limb (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Tracheal dyskinesia (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Dissociative neurological symptom disorder co-occurrent with symptoms of gait disorder (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Acquired choreiform dyspraxia |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Musculocutaneous nerve palsy |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Psychogenic tremor (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Injury to a joint due to an extension beyond the normal range of motion |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Injury to a joint due to flexion of a joint beyond its normal range of movement. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Contracture of muscle following injury |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paralysis of cervical sympathetic trunk (disorder) |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Crutch paralysis |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Chorea due to and following encephalitis |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Cranial nerve palsy due to diabetes mellitus |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Akathisia |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare neurologic disease characterized by the manifestation of an underlying psychiatric illness or malingering, and that cannot be attributed to any known structural or neurochemical diseases. Most cases fall in the psychiatric diagnostic category of conversion disorder, also referred to as functional neurological symptom disorder. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare genetic neurological disorder characterized by infantile hypotonia, congenital ophthalmic anomalies (including strabismus, esotropia, nystagmus, and central visual impairment), global developmental delay and intellectual disability, behavioral abnormalities, and movement disorder (such as dystonia, chorea, hyperkinesia, stereotypies). Mild facial dysmorphism and skeletal deformities have also been reported. EEG testing shows marked abnormalities in the absence of overt epileptic seizures. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A rare lethal multiple congenital anomalies/dysmorphic syndrome characterized by the association of fetal akinesia sequence, bilateral microphthalmia, microtia, and persistent truncus arteriosus. Additional dysmorphic features include prominent forehead, small nose, micrognathia, as well as camptodactyly and symphalangism. Contractures of large joints and micropenis have also been reported. |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Psychogenic dyskinesia |
Is a |
False |
Movement disorder |
Inferred relationship |
Some |
|
Optic ataxia |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Oculomotor nerve synkinesis |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paralysis of diaphragm |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paralysis of tongue |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paralysis due to lesion of spinal cord (disorder) |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paralysis of palate |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paralytic syndrome |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
A painful restriction of joint motion caused by excessive scarring following injury or operative procedure. |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Paralytic shellfish poisoning |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|
Aspergillus clavatus tremors |
Is a |
True |
Movement disorder |
Inferred relationship |
Some |
|