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Translation of "syndrome de polypose " (French → English) :
TERMINOLOGY
see also In-Context Translations below syndrome de polypose multiple familiale
Polyposis coli
SNOMEDCT-BE (disorder) / 72900001
SNOMEDCT-BE (disorder) / 72900001
cap polypose
Cap polyposis (CP) is characterised by multiple inflammatory polyps that predominantly affect the rectosigmoid area and manifest primarily as rectal bleeding with abnormal transit, constipation or diarrhoea. To date, around 67 cases have been describ
SNOMEDCT-BE (disorder) / 720604008
SNOMEDCT-BE (CP) is characterised by multiple inflammatory polyps that predominantly affect the rectosigmoid area and manifest primarily as rectal bleeding with abnormal transit, constipation or diarrhoea. To date, around 67 cases have been describ / 7206
syndrome | syndrome
syndrome
UGENT - Medical terms -
UGENT - Medical terms -
syndrome d'atrophie spinale-ophtalmoplégie-syndrome pyramidal
Hamano Tsukamoto syndrome
SNOMEDCT-BE (disorder) / 771238004
SNOMEDCT-BE (disorder) / 771238004
syndrome de déficience intellectuelle liée à l'X-syndrome cranio-facio-squelettique
A rare hereditary syndromic intellectual disability with characteristics of craniofacial and skeletal abnormalities in association with mild intellectual disability in females and early postnatal lethality in males. In addition to mild cognitive impa
SNOMEDCT-BE (disorder) / 773274001
SNOMEDCT-BE (disorder) / 773274001
syndrome de neuropathie périphérique-leucodystrophie centrale dysmyélinisante-syndrome de Waardenburg-maladie de Hirschsprung
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
SNOMEDCT-BE (disorder) / 765325002
SNOMEDCT-BE (disorder) / 765325002
syndrome de dérèglement immunitaire-maladie inflammatoire de l'intestin-arthrite-infections récurrentes
Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome
SNOMEDCT-BE (disorder) / 771333006
SNOMEDCT-BE (disorder) / 771333006
syndrome d'appendice caudal-surdité
Syndrome with characteristics of caudal appendage, short terminal phalanges, deafness, cryptorchidism, intellectual deficit, short stature and dysmorphism. It has been described in monozygotic twin boys.
SNOMEDCT-BE (disorder) / 726621009
SNOMEDCT-BE (disorder) / 726621009
syndrome faciodigitogénital autosomique récessif
Aarskog-like syndrome
SNOMEDCT-BE (disorder) / 725434009
SNOMEDCT-BE (disorder) / 725434009
syndrome Noonan-like avec cheveux anagènes caducs
A Noonan-related syndrome with characteristics of facial anomalies suggestive of Noonan syndrome, a distinctive hair anomaly described as loose anagen hair syndrome, frequent congenital heart defects, distinctive skin features with darkly pigmented s
SNOMEDCT-BE (disorder) / 723444009
SNOMEDCT-BE (disorder) / 723444009
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syndrome de polypose
Date index:2021-10-24 -
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