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5p-syndrome
Artificial chromosome
B1 deletion syndrome
Cat cry syndrome
Chromosomal aberration
Chromosomal abnormality
Chromosomal deletion
Chromosome 5 short arm deletion
Chromosome aberration
Chromosome abnormality
Chromosome anomaly
Chromosome deletion
Cri du chat syndrome
Crying cat syndrome
Deletion of short arm of chromosome 4
Deletion of short arm of chromosome 5
Lejeune syndrome
Synthesized chromosome
Synthetic chromosome

Translation of "chromosomal deletion " (English → French) :

chromosomal deletion

délétion chromosomique
IATE - Health
IATE - Health


chromosome deletion

carence de chromosome | déficience chromosomique | délétion chromosomique
IATE - Health
IATE - Health


cri du chat syndrome | cat cry syndrome | crying cat syndrome | deletion of short arm of chromosome 5 | B1 deletion syndrome

syndrome du cri du chat | syndrome plurimalformatif de Lejeune | maladie du cri du chat | syndrome de Lejeune
biologie > embryologie | médecine > sémiologie et pathologie
biologie > embryologie | médecine > sémiologie et pathologie


A rare chromosomal anomaly syndrome resulting from a partial interstitial deletion of the short arm of chromosome 9. The disease has characteristics of mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivi

syndrome de microdélétion 9p13
SNOMEDCT-BE (disorder) / 764725008
SNOMEDCT-BE (disorder) / 764725008


A rare chromosomal anomaly syndrome resulting from a partial deletion of the long arm of chromosome 10. The disease has a highly variable phenotype with principle characteristics of developmental delay (usually of language and speech), variable cogni

monosomie non distale 10q
SNOMEDCT-BE (usually of language and speech), variable cogni / 770665005
SNOMEDCT-BE (disorder) / 770665005


5p-syndrome | chromosome 5 short arm deletion | cri du chat syndrome | Lejeune syndrome

maladie du cri du chat
IATE - Health
IATE - Health


Deletion of short arm of chromosome 4

Délétion du bras court du chromosome 4
WORLD HEALTH ORGANIZATION ICD-10: Q93.3
WORLD HEALTH ORGANIZATION ICD-10: Q93.3


chromosomal aberration | chromosomal abnormality | chromosome aberration | chromosome abnormality | chromosome anomaly

aberration chromosomique | anomalie chromosomique | aberration des chromosomes | remaniement chromosomique
biologie > génie génétique
biologie > génie génétique


artificial chromosome | synthetic chromosome | synthesized chromosome

chromosome artificiel | chromosome synthétique | chromosome de synthèse
biologie > génie génétique | biologie > cytogénétique
biologie > génie génétique | biologie > cytogénétique


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

trisomie distale 20q
SNOMEDCT-BE (ventricular septal defect, coarc / 764500002
SNOMEDCT-BE (disorder) / 764500002




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'chromosomal deletion'

Date index:2021-11-05 -

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