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Ablepharon Absence or agenesis of cilia
Accessory eye muscle
Birth defect
Congenital abnormality
Congenital anomaly
Congenital cardiac malformation
Congenital defect
Congenital deformity
Congenital disease
Congenital disorder
Congenital malformation
Congenital malformations of lips
Eyelid

Vertaling van "congenital malformations lips " (Engels → Nederlands) :

birth defect | congenital anomaly | congenital defect | congenital disease | congenital disorder | congenital malformation

aangeboren aandoening


congenital disease [ congenital deformity | congenital malformation ]

aangeboren ziekte [ aangeboren afwijking ]


birth defect | congenital abnormality | congenital malformation

aangeboren afwijking | aangeboren anomalieën | congenitale deformatie | geboorteafwijking


Congenital malformations of lips

congenitale misvormingen van lippen


Anisocoria, congenital Atresia of pupil Congenital malformation of iris NOS Corectopia

anisocorie, congenitaal | congenitale misvorming van iris NNO | corectopie | pupilatresie


Ablepharon Absence or agenesis of:cilia | eyelid | Accessory:eye muscle | Blepharophimosis, congenital Coloboma of eyelid Congenital malformation of eyelid NOS

ablefarie | accessoir | ooglid | accessoir | oogspier | blepharophimosis, congenitaal | coloboom van ooglid | congenitale misvorming van ooglid NNO | ontbreken of agenesie van | oogharen | ontbreken of agenesie van | ooglid


An extremely rare multiple congenital malformation syndrome with the association of ablepharon, macrostomia, abnormal external ears, syndactyly of the hands and feet, skin findings (such as dry and coarse skin or redundant folds of skin), absent or s

ablefaron, macrostomiesyndroom


A genetic non-syndromic congenital malformation of the neurenteric canal, spinal cord and column characterized by progressive neurologic deterioration (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal

primair gekluisterd ruggenmerg-syndroom


A very rare congenital malformation of the digits with the absence of the middle phalanges (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families.

brachydactylie type A5


congenital cardiac malformation

congenitale hartafwijking




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Date index: 2021-02-25
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