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Arnold-Chiari malformation
Cerebellar ectopia
Chiari I herniation
Chiari I malformation
Chiari malformation
Chiari malformation type I
Congenital absence of vertebra
Congenital diverticulum of left ventricle
Dysgenesis
Fusion of spine
Hemivertebra
Herniation of the cerebellar tonsils
Hindbrain herniation
Kyphosis
Lordosis
Malformation
Malformation of lumbosacral
Malformation of myocardium
Malformation of spine
Malformation of the bladder
Malposition of heart Uhl's disease
Myocardium+
Oesophagus+
Pericardium
Pericardium+
Platyspondylisis
Supernumerary vertebra
Thyroid gland+
Tuberculosis of endocardium+
Tuberculous cerebral arteritis+
Unspecified or not associated with scoliosis
Vesical malformation

Vertaling van "malformation myocardium " (Engels → Nederlands) :

Congenital:diverticulum of left ventricle | malformation of:myocardium | pericardium | Malposition of heart Uhl's disease

congenitale | divertikel van linker ventrikel | congenitale | misvorming van | myocard | congenitale | misvorming van | pericard | liggingsafwijking van hart | ziekte van Uhl


malformation of the bladder | vesical malformation

misvorming van de blaas


Chiari I herniation | Chiari I malformation | Chiari malformation type I

Chiari type 1 malformatie


Arnold-Chiari malformation | cerebellar ectopia | Chiari malformation | herniation of the cerebellar tonsils | hindbrain herniation

Chiari malformatie


dysgenesis | malformation

dysgenesie | gebrekkige ontwikkeling




A rare genetic multiple congenital anomalies syndrome with characteristics of second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing

branchio-otisch syndroom


Congenital:absence of vertebra | fusion of spine | kyphosis | lordosis | malformation of lumbosacral (joint) (region) | Hemivertebra | Malformation of spine | Platyspondylisis | Supernumerary vertebra | unspecified or not associated with scoliosis

congenitale | kyfose | niet-gespecificeerd of niet verband houdend met scoliose | congenitale | lordose | niet-gespecificeerd of niet verband houdend met scoliose | congenitale | misvorming van lumbosacraal (gewricht) gebied | niet-gespecificeerd of niet verband houdend met scoliose | congenitale | ontbreken van wervel | niet-gespecificeerd of niet verband houdend met scoliose | congenitale | vergroeiing van wervelkolom | niet-gespecificeerd of niet verband houdend met scoliose | extra wervelniet-gespecificeerd of niet verband houdend met scoliose | hemivertebraniet-gespecificeerd of niet verband houdend met scoliose | misvorming van wer ...[+++]


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

mozaïektrisomie 9


Tuberculosis of:endocardium+ (I39.8*) | myocardium+ (I41.0*) | oesophagus+ (K23.0*) | pericardium+ (I32.0*) | thyroid gland+ (E35.0*) | Tuberculous cerebral arteritis+ (I68.1*)

tuberculeuze cerebrale arteriitis (I68.1) | tuberculose van | endocard (I39.8) | tuberculose van | myocard (I41.0) | tuberculose van | oesofagus (K23.0) | tuberculose van | pericard (I32.0) | tuberculose van | schildklier (E35.0)


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