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Translation of "maladie récessive autosomique " (French → English) :
TERMINOLOGY
see also In-Context Translations below maladie lymphoproliférative autosomique récessive
Autosomal recessive lymphoproliferative disease
SNOMEDCT-BE (disorder) / 771309000
SNOMEDCT-BE (disorder) / 771309000
maladie de Charcot-Marie-Tooth intermédiaire autosomique récessive type B
An extremely rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c
SNOMEDCT-BE (disorder) / 773330000
SNOMEDCT-BE (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c / 773330000
maladie de Charcot-Marie-Tooth intermédiaire autosomique récessive type C
A rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease with characteristics of childhood to adulthood-onset of progressive, moderate to severe, predominantly distal, mostly lower limb muscle weakness and atrophy, foot de
SNOMEDCT-BE (disorder) / 773414009
SNOMEDCT-BE (CMT) disease with characteristics of childhood to adulthood-onset of progressive, moderate to severe, predominantly distal, mostly lower limb muscle weakness and atrophy, foot de / 773414009
maladie de Charcot-Marie-Tooth autosomique récessive avec raucité de la voix
Autosomal recessive axonal Charcot-Marie-Tooth disease type 2K
SNOMEDCT-BE (disorder) / 725047007
SNOMEDCT-BE (disorder) / 725047007
maladie du motoneurone inférieur autosomique récessive de l'enfance
Autosomal recessive distal spinal muscular atrophy type 4
SNOMEDCT-BE (disorder) / 771302009
SNOMEDCT-BE (disorder) / 771302009
Ataxie (de):cérébelleuse précoce avec:myoclonies [Ramsay-Hunt] | persistance des réflexes tendineux | tremblement essentiel | Friedreich (autosomique récessive) | spino-cérébelleuse récessive liée au chromosome X
Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia
WORLD HEALTH ORGANIZATION ICD-10: G11.1
WORLD HEALTH ORGANIZATION ICD-10: G11.1
ataxie cérébelleuse autosomique récessive avec spasticité tardive
Autosomal recessive cerebellar ataxia with late-onset spasticity
SNOMEDCT-BE (disorder) / 763348005
SNOMEDCT-BE (disorder) / 763348005
anémie sidéroblastique autosomique récessive de l'adulte
Adult-onset autosomal recessive sideroblastic anemia
SNOMEDCT-BE (disorder) / 720465002
SNOMEDCT-BE (disorder) / 720465002
omodysplasie autosomique récessive
Autosomal recessive omodysplasia
SNOMEDCT-BE (disorder) / 725166005
SNOMEDCT-BE (disorder) / 725166005
amélie autosomique récessive
Autosomal recessive amelia
SNOMEDCT-BE (disorder) / 726735000
SNOMEDCT-BE (disorder) / 726735000
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maladie récessive autosomique
Date index:2023-06-23 -
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