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Asphyxia by gag
Assault by gagging
GAG - Glycosaminoglycan

Translation of "o e gag reflex " (English → French) :

O/E - gag reflex
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à l'examen : réflexe pharyngé
SNOMEDCT-CA (constatation) / 274300005
SNOMEDCT-CA (constatation) / 274300005
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GAG - Glycosaminoglycan
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mucopolysaccharide
SNOMEDCT-BE (substance) / 82565009
SNOMEDCT-BE (substance) / 82565009
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Assault by gagging
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agression par bâillonnement
SNOMEDCT-BE (event) / 242935006
SNOMEDCT-BE (event) / 242935006
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Asphyxia by gag
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asphyxie par un bâillon
SNOMEDCT-BE (event) / 242021006
SNOMEDCT-BE (event) / 242021006
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Syndrome with characteristics of precocious puberty (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa
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syndrome de parésie spastique-puberté précoce
SNOMEDCT-BE (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa / 732958004
SNOMEDCT-BE (disorder) / 732958004
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This syndrome is characterized by psychomotor delay and severe myopathy (hypotonia, absent tendon reflexes and delayed myelination) from birth, associated with hypermethioninemia and elevated serum creatine kinase levels. It has been described in thr
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retard psychomoteur par déficit en S-adénosylhomocystéine hydrolase
SNOMEDCT-BE (hypotonia, absent tendon reflexes and delayed myelination) from birth, associated with hypermethioninemia and elevated serum creatine kinase levels. It has been described in thr / 724039002
SNOMEDCT-BE (disorder) / 724039002
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A genetic non-syndromic congenital malformation of the neurenteric canal, spinal cord and column characterised by progressive neurologic deterioration (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal
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fibrolipome du filum
SNOMEDCT-BE (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal / 768939009
SNOMEDCT-BE (disorder) / 768939009
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A rare distal hereditary motor neuropathy with characteristics of slowly progressive atrophy and weakness of distal muscles of hands and feet with normal deep tendon reflexes or absent ankle reflexes and minimal or no sensory loss, sometimes mild pro
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atrophie musculaire spinale distale liée à l'X type 3
SNOMEDCT-BE (disorder) / 766764008
SNOMEDCT-BE (disorder) / 766764008
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A genetic non-syndromic congenital malformation of the neurenteric canal, spinal cord and column characterized by progressive neurologic deterioration (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal
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syndrome de la moelle attachée primaire
SNOMEDCT-BE (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal / 768939009
SNOMEDCT-BE (disorder) / 768939009
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Jeavons syndrome is an idiopathic generalised form of reflex epilepsy characterised by childhood onset, unique seizure manifestations, striking light sensitivity, and possible occurrence of generalised tonic-clonic seizures. Onset occurs in childhood
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syndrome de Jeavons
SNOMEDCT-BE (disorder) / 716278005
SNOMEDCT-BE (disorder) / 716278005
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Others have searched : asphyxia by gag    assault by gagging    gag glycosaminoglycan    o e gag reflex    


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'o e gag reflex'

Date index:2023-08-01 -

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