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Monosomy 12p12.1
Monosomy 13q12.3
Monosomy 14q11.2
Monosomy 15q11.2
Monosomy 16q24.1
Monosomy 1p31p32
Monosomy 8p11.2
Monosomy 8q21.11

Translation of "monosomy 8q21 " (English → French) :

Monosomy 8q21.11
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syndrome de microdélétion 8q21.11
SNOMEDCT-BE (disorder) / 718615003
SNOMEDCT-BE (disorder) / 718615003
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https://browser.ihtsdotools.or (...) [HTML]
A subgroup of therapy-related myeloid neoplasms (t-MN), associated with treatment of an unrelated neoplastic disease with radiation. The neoplastic cells typically harbor unbalanced aberrations of chromosomes 5 and 7 (monosomy 5/del(5q) and monosomy
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leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux radiations
SNOMEDCT-BE (t-MN), associated with treatment of an unrelated neoplastic disease with radiation. The neoplastic cells typically harbor unbalanced aberrations of chromosomes 5 and 7 (monosomy 5/del(5q) and monosomy / 766048008
SNOMEDCT-BE (disorder) / 766048008
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https://browser.ihtsdotools.or (...) [HTML]
Monosomy 8p11.2
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syndrome de délétion 8p11.2
SNOMEDCT-BE (disorder) / 719646006
SNOMEDCT-BE (disorder) / 719646006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A partial autosomal monosomy with characteristics of a variable combination of developmental delay, intellectual disability, ectodermal, genitourinary and minor cardiac anomalies and specific dysmorphic features (prominent forehead and low-set ears).
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monosomie non distale 12q
SNOMEDCT-BE (prominent forehead and low-set ears). / 782694003
SNOMEDCT-BE (disorder) / 782694003
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https://browser.ihtsdotools.or (...) [HTML]
Monosomy 15q11.2
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syndrome de microdélétion 15q11.2
SNOMEDCT-BE (disorder) / 771340007
SNOMEDCT-BE (disorder) / 771340007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Monosomy 12p12.1
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syndrome de microdélétion 12p12.1
SNOMEDCT-BE (disorder) / 778007004
SNOMEDCT-BE (disorder) / 778007004
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Monosomy 16q24.1
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syndrome de microdélétion 16q24.1
SNOMEDCT-BE (disorder) / 770760006
SNOMEDCT-BE (disorder) / 770760006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Monosomy 13q12.3
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome de microdélétion 13q12.3
SNOMEDCT-BE (disorder) / 773547003
SNOMEDCT-BE (disorder) / 773547003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Monosomy 14q11.2
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome de microdélétion 14q11.2
SNOMEDCT-BE (disorder) / 719047001
SNOMEDCT-BE (disorder) / 719047001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Monosomy 1p31p32
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome de microdélétion 1p31p32
SNOMEDCT-BE (disorder) / 766766005
SNOMEDCT-BE (disorder) / 766766005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : monosomy 12p12    monosomy 13q12    monosomy 14q11    monosomy 15q11    monosomy 16q24    monosomy 1p31p32    monosomy 8p11    monosomy 8q21    


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'monosomy 8q21'

Date index:2023-12-14 -

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