A rare chromosomal anomaly syndrome resulting from the partial trisomy of the long arm of chromosome 9. The disease has a highly variable phenotype principally characterised by developmental delay, short stature, intellectual disability and craniofac

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

duplication non distale 9q

SNOMEDCT-BE (disorder) / 764997000

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

A rare chromosomal anomaly syndrome resulting from partial trisomy of the long arm of chromosome 20 with high phenotypic variability. The disease has characteristics of neurodevelopmental delay, cardiac malformations (ventricular septal defect, coarc

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trisomie distale 20q

SNOMEDCT-BE (ventricular septal defect, coarc / 764500002

SNOMEDCT-BE (disorder) / 764500002

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Whole chromosome trisomy, mosaicism (mitotic nondisjunction)

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Trisomie d'un chromosome entier, mosaïque chromosomique (non-disjonction mitotique)

WORLD HEALTH ORGANIZATION ICD-10: Q92.1

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Whole chromosome trisomy, meiotic nondisjunction

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Trisomie d'un chromosome entier, non-disjonction méïotique

WORLD HEALTH ORGANIZATION ICD-10: Q92.0

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in t

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déficit combiné en facteurs V et VIII

SNOMEDCT-BE (chromosome 18; q21) or in t / 715559004

SNOMEDCT-BE (disorder) / 715559004

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trisomy groupe E no.17-18

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

trisomie 17-18

IATE - Health

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

Others have searched : trisomy + syndrome e-trisomy edward's syndrome edwards syndrome whole chromosome trisomy meiotic nondisjunction chromosome 18 trisomy trisomy 16-18 trisomy 16-18 syndrome trisomy 18 syndrome trisomy e syndrome trisomy groupe e no 17-18 Chromosome 18 trisomy

www.wordscope.com (v4.0.br.77)

'Chromosome 18 trisomy'

Date index:2021-07-05 -

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Translation of "Chromosome 18 trisomy " (English → French) :

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