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Bernard-Soulier
Bessel-Hagen disease
Chronic progressive chorea
Chronic progressive hereditary chorea
Degeneration
Degenerative chorea
Disease
Familial spastic paralysis
Friedreich disease
Friedreich familial ataxia
Friedreich hereditary ataxia
Friedreich hereditary spinal ataxia
Friedreich spinocerebella
Friedreich's ataxia
Friedreich's disease
Friedreich's familial ataxia
Friedreich's hereditary ataxia
Friedreich's hereditary spinal ataxia
Giant platelet
HD
HSP
Hb-M
Hereditary cerebellar ataxia NOS
Hereditary chorea
Hereditary deforming chondrodysplasia
Hereditary disease
Hereditary disease linked with the sex
Hereditary multiple exostosis
Hereditary spastic paraplegia
Huntington chorea
Huntington disease
Huntington's chorea
Huntington's disease
Inherited disease
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas
Strümpell's disease
Syndrome

Translation of "disease methaemoglobinaemia hereditary " (English → French) :

Congenital NADH-methaemoglobin reductase deficiency Haemoglobin-M [Hb-M] disease Methaemoglobinaemia, hereditary

Déficit congénital en NADH-méthémoglobine-réductase Hémoglobinose M [Hb-M] Méthémoglobinémie héréditaire
WORLD HEALTH ORGANIZATION ICD-10: D74.0
WORLD HEALTH ORGANIZATION ICD-10: D74.0


Friedreich's ataxia [ Friedreich's disease | Friedreich disease | Friedreich's hereditary spinal ataxia | Friedreich hereditary spinal ataxia | Friedreich familial ataxia | Friedreich's familial ataxia | Friedreich hereditary ataxia | Friedreich's hereditary ataxia | Friedreich spinocerebella ]

ataxie de Friedreich [ maladie de Friedreich | ataxie héréditaire ]
Nervous System
Système nerveux


Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas

chondrodysplasie déformante héréditaire | maladie de Bessel-Hagen | maladie des exostoses multiples | maladie exostosante | maladie ostéogénique | ostéochondromes multiples
IATE - Health
IATE - Health


inherited disease [ hereditary disease ]

maladie héréditaire
Human Diseases - Various | Animal Diseases
Maladies humaines diverses | Maladies des animaux


Huntington's chorea | chronic progressive hereditary chorea | chronic progressive chorea | degenerative chorea | hereditary chorea | Huntington's disease | HD

chorée de Huntington | chorée héréditaire | chorée chronique | maladie de Huntington
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique


chronic progressive hereditary chorea | Huntington chorea | Huntington disease | Huntington's chorea | Huntington's disease | HD [Abbr.]

chorée de Huntington | chorée d'Huntington | chorée héréditaire | maladie de Huntington
IATE - Health
IATE - Health


hereditary spastic paraplegia [ HSP | familial spastic paralysis | Strümpell's disease ]

paraplégie spastique familiale [ maladie de Strümpell-Lorrain | paraplégie spasmodique familiale de Strümpell-Lorrain ]
Nervous System | Human Diseases - Various
Système nerveux | Maladies humaines diverses


hereditary disease linked with the sex

maladie héréditaire liée au sexe
IATE - Health
IATE - Health


Hereditary cerebellar:ataxia NOS | degeneration | disease | syndrome

Ataxie SAI | Dégénérescence | Maladie | Syndrome | cérébelleux (cérébelleuse) héréditaire
WORLD HEALTH ORGANIZATION ICD-10: G11.9
WORLD HEALTH ORGANIZATION ICD-10: G11.9


Bernard-Soulier [giant platelet] syndrome Glanzmann's disease Grey platelet syndrome Thromboasthenia (haemorrhagic)(hereditary) Thrombocytopathy

Maladie de Glanzmann Syndrome de(s):Bernard-Soulier [plaquettes géantes] | plaquettes grises | Thrombasthénie (hémorragique) (héréditaire) Thrombopathie
WORLD HEALTH ORGANIZATION ICD-10: D69.1
WORLD HEALTH ORGANIZATION ICD-10: D69.1




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'disease methaemoglobinaemia hereditary'

Date index:2022-09-09 -

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