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Accident caused by earth surface movement
Accident caused by movement of earth's crust
Movement disorder

Translation of "Movement disorder " (English → French) :

A movement disorder with manifestation of episodes of involuntary tremor of the chin and lower lip. The disorder has been described in less than 25 families from Europe and the USA, with a slight male preponderance. Onset usually occurs in childhood
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géniospasme héréditaire
SNOMEDCT-BE (disorder) / 718103001
SNOMEDCT-BE (disorder) / 718103001
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Movement disorder
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trouble du mouvement
SNOMEDCT-BE (disorder) / 60342002
SNOMEDCT-BE (disorder) / 60342002
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A rare paroxysmal movement disorder with episodes of sustained, conjugate, upward deviation of the eyes and down beating saccades in attempted downgaze (with preserved horizontal eye movements). This is accompanied by ataxic symptoms (unsteady gait,
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syndrome d'Ouvrier-Billson
SNOMEDCT-BE (disorder) / 763127004
SNOMEDCT-BE (disorder) / 763127004
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A paroxysmal dystonic movement disorder occurring in association with gastro-oesophageal reflux, and, in some cases, hiatal hernia. The prevalence is unknown. Onset usually occurs during infancy or early childhood. The dystonic movements are characte
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syndrome de Sandifer
SNOMEDCT-BE (disorder) / 230314007
SNOMEDCT-BE (disorder) / 230314007
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A form of neuroacanthocytosis with clinical characteristics of a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx anti
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syndrome de McLeod
SNOMEDCT-BE (disorder) / 724172004
SNOMEDCT-BE (disorder) / 724172004
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A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on
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ataxie spinocérébelleuse type 26
SNOMEDCT-BE (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on / 718769009
SNOMEDCT-BE (disorder) / 718769009
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Characterized by marked neonatal hypotonia, progressive quadriparesis, severely delayed developmental milestones (walking at 3 years of age), gastroesophageal reflux, and stereotypic movements of the hands, esotropia and infantile autism. It has been
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déficience intellectuelle liée à l'X type Cantagrel
SNOMEDCT-BE (walking at 3 years of age), gastroesophageal reflux, and stereotypic movements of the hands, esotropia and infantile autism. It has been / 719016007
SNOMEDCT-BE (disorder) / 719016007
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Accident caused by movement of earth's crust
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accident causé par un mouvement de la croûte terrestre
SNOMEDCT-BE (event) / 242558003
SNOMEDCT-BE (event) / 242558003
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Accident caused by earth surface movement
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accident causé par le mouvement de la surface de la terre
SNOMEDCT-BE (event) / 217736003
SNOMEDCT-BE (event) / 217736003
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https://browser.ihtsdotools.or (...) [HTML]
A rare neurologic disease characterized by global developmental delay, intellectual disability, multiple ischemic lesions on brain MRI, behavioral abnormalities, dystonia, choreic movements and pyramidal syndrome, facial dysmorphism (hypertelorism, a
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syndrome autosomique récessif de leucoencéphalopathie-infarctus cérébraux-rétinite pigmentaire
SNOMEDCT-BE (hypertelorism, a / 771476007
SNOMEDCT-BE (disorder) / 771476007
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'Movement disorder'

Date index:2021-02-15 -

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