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Calcification
Hardening
Hypoplasia
Tissue or organ underdevelopment

Translation of "hypoplasia and calcification " (English → French) :

A form of syndromic craniosynostosis with characteristics of craniosynostosis, mild facial dysmorphism (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a f
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syndrome de craniosynostose-calcifications intracrâniennes
SNOMEDCT-BE (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a f / 720816004
SNOMEDCT-BE (disorder) / 720816004
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A very rare genetic vascular disease of autosomal recessive inheritance, described in less than 20 patients to date. The disease has manifestations of adult-onset (as early as the second decade of life) isolated calcification of the arteries of the l
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syndrome héréditaire de calcification artérielle et articulaire
SNOMEDCT-BE (as early as the second decade of life) isolated calcification of the arteries of the l / 718602007
SNOMEDCT-BE (disorder) / 718602007
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hypoplasia | tissue or organ underdevelopment
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hypoplasie | développement insuffisant d'un tissu ou d'un organe
UGENT - Medical terms -
UGENT - Medical terms -
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http://users.ugent.be/~rvdstic (...) [HTML]
A subtype of junctional epidermolysis bullosa (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A ge
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epidermolyse bulleuse jonctionnelle type non-Herlitz
SNOMEDCT-BE (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A ge / 724225008
SNOMEDCT-BE (disorder) / 724225008
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https://browser.ihtsdotools.or (...) [HTML]
A rare genetic ocular disease with characteristics of congenital nystagmus (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an
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syndrome d'hypoplasie fovéale-cataracte présénile
SNOMEDCT-BE (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an / 778042000
SNOMEDCT-BE (disorder) / 778042000
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https://browser.ihtsdotools.or (...) [HTML]
A rare genetic developmental defect during embryogenesis syndrome with characteristics of postaxial polydactyly and other abnormalities of the hands and feet (for example brachydactyly, broad toes), hypoplasia and fusion of the vertebral bodies, as w
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syndrome de polydactylie postaxiale-anomalies dentaires et vertébrales
SNOMEDCT-BE (for example brachydactyly, broad toes), hypoplasia and fusion of the vertebral bodies, as w / 773279006
SNOMEDCT-BE (disorder) / 773279006
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https://browser.ihtsdotools.or (...) [HTML]
Aplasia and hypoplasia of cementum Dilaceration of tooth Enamel hypoplasia (neonatal)(postnatal)(prenatal) Regional odontodysplasia Turner's tooth
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Aplasie et hypoplasie du cément Dent hypoplasique de Turner Dislocation du germe dentaire Hypoplasie de l'émail (néonatale) (post-natale) (prénatale) Odontodysplasie régionale
WORLD HEALTH ORGANIZATION ICD-10: K00.4
WORLD HEALTH ORGANIZATION ICD-10: K00.4
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
A form of non-rhizomelic chondrodysplasia punctata, a primary bone dysplasia, with characteristics of hypoplasia of the distal phalanges of the fingers, nasal hypoplasia, epiphyseal stippling appearing in the first year of life, as well as mild and n
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chondrodysplasie ponctuée avec brachytéléphalangie
SNOMEDCT-BE (disorder) / 778067002
SNOMEDCT-BE (disorder) / 778067002
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calcification | hardening
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calcification | 1) formation des os - 2) durcissement d'une artère | d'une articulation
UGENT - Medical terms -
UGENT - Medical terms -
http://users.ugent.be/~rvdstic (...) (...) [HTML]
http://users.ugent.be/~rvdstic (...) [HTML]
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome
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syndrome de dysplasie spondylo-épimétaphysaire-membres courts-anomalies de calcification
SNOMEDCT-BE (disorder) / 766821006
SNOMEDCT-BE (disorder) / 766821006
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https://browser.ihtsdotools.or (...) [HTML]


Others have searched : calcification    hardening    hypoplasia    tissue or organ underdevelopment    hypoplasia and calcification    


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'hypoplasia and calcification'

Date index:2023-02-17 -

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