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Aseptic necrosis of bone
Bone necrosis
Bone tissue of vomer bone
Gangrene
Necrosis

Translation of "Bone necrosis " (English → Dutch) :

Bone necrosis
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botnecrose
SNOMEDCT-BE (disorder) / 240196003
SNOMEDCT-BE (disorder) / 240196003
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https://browser.ihtsdotools.or (...) [HTML]
Aseptic necrosis of bone
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aseptische botnecrose
SNOMEDCT-BE (disorder) / 398199007
SNOMEDCT-BE (disorder) / 398199007
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https://browser.ihtsdotools.or (...) [HTML]
necrosis | gangrene
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necrose | weefselversterf
UGENT - Medical terms -
UGENT - Medical terms -
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http://users.ugent.be/~rvdstic (...) [HTML]
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
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progressieve ossale heteroplasie
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
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https://browser.ihtsdotools.or (...) [HTML]
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
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intra-osseus hemangioom
SNOMEDCT-BE (disorder) / 764100007
SNOMEDCT-BE (disorder) / 764100007
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https://browser.ihtsdotools.or (...) [HTML]
Bone tissue of vomer bone
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botweefsel van vomer
SNOMEDCT-BE (body structure) / 427621007
SNOMEDCT-BE (body structure) / 427621007
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https://browser.ihtsdotools.or (...) [HTML]
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
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congenitale amegakaryocytische trombocytopenie
SNOMEDCT-BE (disorder) / 716336002
SNOMEDCT-BE (disorder) / 716336002
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https://browser.ihtsdotools.or (...) [HTML]
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
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syndroom van Verloove-Vanhorick-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
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https://browser.ihtsdotools.or (...) [HTML]
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
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obesitas als gevolg van melanocortine-4-receptordeficiëntie
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
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https://browser.ihtsdotools.or (...) [HTML]
Carpotarsal osteochondromatosis is a very rare primary bone dysplasia disorder with characteristics of abnormal bone proliferation and osteochondromas in the upper and lower limbs.
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carpotarsale osteochondromatose
SNOMEDCT-BE (disorder) / 389272007
SNOMEDCT-BE (disorder) / 389272007
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https://browser.ihtsdotools.or (...) [HTML]


Others have searched : aseptic necrosis of bone    bone necrosis    bone tissue of vomer bone    gangrene    necrosis    Bone necrosis    


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'Bone necrosis'

Date index:2022-08-21 -

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