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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A recently described syndrome associated with variable developmental delay, facial dysmorphism, seizures and autistic spectrum disorder. This syndrome is caused by an interstitial deletion encompassing 16q24.3. They vary in size the common region of

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del(16)(q24.3)

SNOMEDCT-BE (disorder) / 719580004

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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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Monosomy 8p11.2

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syndrome de délétion 8p11.2

SNOMEDCT-BE (disorder) / 719646006

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