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Apte à hériter
Communauté des héritiers
Communauté héréditaire
Défaut héréditaire
Hoirie
Hypersegmentation
Hyposegmentation
Héréditaire
Héréditairement transmissible
Leucomélanopathie héréditaire
Maladie de Glanzmann Syndrome de
Maladie de Glanzmann-Naegeli
May-Hegglin
Paralysie faciale congénitale héréditaire isolée
Pelger-Huët
Plaquettes grises
Plaquettes géantes
Pseudohémophilie héréditaire de Frank
Tare héréditaire
Thrombasthénie de Glanzmann
Thrombasthénie héréditaire
Thrombasthénie type Naegeli
Transmissible par voie héréditaire
Vice héréditaire

Translation of "thrombasthénie héréditaire " (French → English) :

maladie de Glanzmann-Naegeli | pseudohémophilie héréditaire de Frank | thrombasthénie de Glanzmann | thrombasthénie héréditaire | thrombasthénie type Naegeli

Glanzmann's thrombasthenia | hereditary thrombasthenia
IATE - Health
IATE - Health


Maladie de Glanzmann Syndrome de(s):Bernard-Soulier [plaquettes géantes] | plaquettes grises | Thrombasthénie (hémorragique) (héréditaire) Thrombopathie

Bernard-Soulier [giant platelet] syndrome Glanzmann's disease Grey platelet syndrome Thromboasthenia (haemorrhagic)(hereditary) Thrombocytopathy
WORLD HEALTH ORGANIZATION ICD-10: D69.1
WORLD HEALTH ORGANIZATION ICD-10: D69.1


défaut héréditaire | tare héréditaire | vice héréditaire

hereditary defect
IATE - AGRICULTURE, FORESTRY AND FISHERIES | Health
IATE - AGRICULTURE, FORESTRY AND FISHERIES | Health


apte à hériter | héréditaire | héréditairement transmissible | transmissible par voie héréditaire

inheritable
IATE - LAW
IATE - LAW


thrombasthénie de Glanzmann

Glanzmann's disease
SNOMEDCT-BE (disorder) / 32942005
SNOMEDCT-BE (disorder) / 32942005


Anomalie (granulation) (granulocyte) ou syndrome de:Alder | May-Hegglin | Pelger-Huët | Hypersegmentation | Hyposegmentation | leucocytaire, héréditaire | Leucomélanopathie héréditaire

Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy
WORLD HEALTH ORGANIZATION ICD-10: D72.0
WORLD HEALTH ORGANIZATION ICD-10: D72.0


communauté héréditaire | communauté des héritiers | hoirie

community of heirs
Droit de la famille - droit héréditaire - droit social (Droit)
Law, legislation & jurisprudence


paralysie faciale congénitale héréditaire isolée

An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or a
SNOMEDCT-BE (disorder) / 733091002
SNOMEDCT-BE (disorder) / 733091002


Adénomatose du côlon Gros intestin SAI Polypose (héréditaire) du côlon

Adenomatosis of colon Large intestine NOS Polyposis (hereditary) of colon
WORLD HEALTH ORGANIZATION ICD-10: D12.6
WORLD HEALTH ORGANIZATION ICD-10: D12.6


neuropathie motrice distale héréditaire de l'adulte jeune

Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006




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thrombasthénie héréditaire

Date index:2023-09-16 -

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