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Sinus carotidien
Souffle carotidien
Syndrome
Syndrome Noonan-like avec cheveux anagènes caducs
Syndrome d'appendice caudal-surdité
Syndrome faciodigitogénital autosomique récessif

Translation of "syndrome carotidien " (French → English) :

SNOMEDCT-BE (body structure) / 21479005
SNOMEDCT-BE (body structure) / 21479005


SNOMEDCT-BE (finding) / 419642000
SNOMEDCT-BE (finding) / 419642000




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 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 d'atrophie spinale-ophtalmoplégie-syndrome pyramidal

Hamano Tsukamoto syndrome
SNOMEDCT-BE (disorder) / 771238004
SNOMEDCT-BE (disorder) / 771238004


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


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




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syndrome carotidien

Date index:2022-09-16 -

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