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Translation of " bone " (English → French) :
TERMINOLOGY
see also In-Context Translations below Progressive osseous heteroplasia (POH) is a rare genetic bone disorder with clinical characteristics of progressive extraskeletal bone formation presenting in early life with cutaneous ossification that progressively involves subcutaneous and then su
hétéroplasie osseuse progressive
SNOMEDCT-BE (POH) is a rare genetic bone disorder with clinical characteristics of progressive extraskeletal bone formation presenting in early life with cutaneous ossification that progressively involves subcutaneous and then su / 719271000
SNOMEDCT-BE (disorder) / 719271000
A rare genetic vascular anomaly with characteristics of severe blood vessel expansion most frequently within the craniofacial bones with painless bone enlargement usually of mandibula, maxilla and/or orbital, nasal and frontal bones. This typically r
malformation veineuse osseuse primaire
SNOMEDCT-BE (disorder) / 764100007
SNOMEDCT-BE (disorder) / 764100007
A rare inherited bone marrow failure syndrome with manifestation of an isolated and severe decrease in the number of platelets and megakaryocytes during the first years of life that develops into bone marrow failure with pancytopenia later in childho
thrombocytopénie amégacaryocytaire congénitale
SNOMEDCT-BE (disorder) / 716336002
SNOMEDCT-BE (disorder) / 716336002
Secondary malignant neoplasm of bone and bone marrow
Tumeur maligne secondaire des os et de la moelle osseuse
WORLD HEALTH ORGANIZATION ICD-10: C79.5
WORLD HEALTH ORGANIZATION ICD-10: C79.5
Fracture of bone following insertion of orthopaedic implant, joint prosthesis, or bone plate
Fracture osseuse après mise en place d'un implant, d'une prothèse articulaire ou d'une plaque d'ostéosynthèse
WORLD HEALTH ORGANIZATION ICD-10: M96.6
WORLD HEALTH ORGANIZATION ICD-10: M96.6
A multiple congenital anomalies/dysmorphic syndrome with characteristics of multiple skeletal malformations (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t
syndrome de Verloove-Van Horick-Brubakk
SNOMEDCT-BE (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t / 764697003
SNOMEDCT-BE (disorder) / 764697003
Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child
obésité par déficit du récepteur de la mélanocortine 4
SNOMEDCT-BE (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child / 717269008
SNOMEDCT-BE (disorder) / 717269008
Bone tissue of vomer bone
tissu osseux de l'os vomer
SNOMEDCT-BE (body structure) / 427621007
SNOMEDCT-BE (body structure) / 427621007
Carpotarsal osteochondromatosis is a very rare primary bone dysplasia disorder with characteristics of abnormal bone proliferation and osteochondromas in the upper and lower limbs.
ostéochondromatose carpo-tarsienne
SNOMEDCT-BE (disorder) / 389272007
SNOMEDCT-BE (disorder) / 389272007
Frontal bone Parietal bone
Os:frontal | pariétal
WORLD HEALTH ORGANIZATION ICD-10: S02.0
WORLD HEALTH ORGANIZATION ICD-10: S02.0
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' bone '
Date index:2021-01-01 -
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