A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are intellectual disability, growth and developmental delay, facial dysmorphism (including microphthalmia, deep-set eyes, low-set, malformed ears, bulbous

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trisomie 9 en mosaïque

SNOMEDCT-BE (including microphthalmia, deep-set eyes, low-set, malformed ears, bulbous / 764989007

SNOMEDCT-BE (disorder) / 764989007

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http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

famille d'ensembles | famille d'ensembles indexée par l'ensemble I | famille de sous-ensembles

mathématiques

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

appareil téléphonique automatique | téléphone automatique | appareil téléphonique à cadran | appareil à cadran | téléphone à cadran

télécommunication > appareil téléphonique

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

An extremely rare autosomal recessive disorder with characteristics of bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears) and strabismus.

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syndrome de paralysie faciale congénitale héréditaire-surdité variable

SNOMEDCT-BE (midfacial retrusion, low-set ears) and strabismus. / 722389002

SNOMEDCT-BE (disorder) / 722389002

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

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'cantor set'

Date index:2022-09-09 -

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Translation of "cantor set " (English → French) :

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