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Becker
Birth defect
CCHS
Congenital anomaly
Congenital central alveolar hypoventilation
Congenital central hypoventilation syndrome
Congenital defect
Congenital deformity
Congenital disease
Congenital disorder
Congenital malformation
Congenital myotonia
Dominant
Drug-induced
Dystrophia myotonica
Early congenital syphilis cutaneous
Early congenital syphilitic laryngitis
Hereditary myotonia
Idiopathic central alveolar hypoventilation
Isaacs
Mucocutaneous
Myotonia chondrodystrophic
Myotonia congenita - autosomal dominant form
Myotonia congenita NOS
Myotonia permanens
Neuromyotonia
Oculopathy
Ondine syndrome
Ondine's Curse
Osteochondropathy
Paramyotonia congenita Pseudomyotonia
Pharyngitis
Pneumonia
Recessive
Rhinitis
Sleep-induced apnea
Steinert
Symptomatic
Thomsen
Thomsen disease
Visceral

Traduction de «congenital myotonia » (Anglais → Néerlandais) :

congenital myotonia | hereditary myotonia | Thomsen disease

myotonia congenita | myotonia hereditaria | paramyotonia congenita | ziekte van Thomsen




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

aangeboren aandoening


Dystrophia myotonica [Steinert] Myotonia:chondrodystrophic | drug-induced | symptomatic | Myotonia congenita:NOS | dominant [Thomsen] | recessive [Becker] | Neuromyotonia [Isaacs] Paramyotonia congenita Pseudomyotonia

dystrophia myotonica [Steinert] | myotonia congenita | NNO | myotonia congenita | dominant [Thomsen] | myotonia congenita | recessief [Becker] | myotonie | chondrodystrofisch | myotonie | door geneesmiddelen | myotonie | symptomatisch | neuromyotonie [Isaacs] | pramyotonia congenita | pseudomyotonie


congenital disease [ congenital deformity | congenital malformation ]

aangeboren ziekte [ aangeboren afwijking ]


congenital central alveolar hypoventilation | congenital central hypoventilation syndrome | idiopathic central alveolar hypoventilation | Ondine syndrome | Ondine's Curse | sleep-induced apnea | CCHS [Abbr.]

congenitaal centraal hypoventilatie-syndroom


Myotonia congenita - autosomal dominant form

congenitale myotonie, autosomale dominante vorm




Late congenital syphilitic interstitial keratitis+ (H19.2*) Late congenital syphilitic oculopathy NEC+ (H58.8*)

late congenitale syfilitische- | interstitiële-keratitis (H19.2) | late congenitale syfilitische- | oculopathie NEC (H58.8)


Early congenital syphilis:cutaneous | mucocutaneous | visceral | Early congenital syphilitic:laryngitis | oculopathy | osteochondropathy | pharyngitis | pneumonia | rhinitis

Elke congenitale syfilitische aandoening gespecificeerd als vroeg of zich manifesterend binnen twee jaar na geboorte. | vroege congenitalesyfilis | cutaan | vroege congenitalesyfilis | mucocutaan | vroege congenitalesyfilis | visceraal | vroege congenitale syfilitische- | faryngitis | vroege congenitale syfilitische- | oculopathie | - | vroege congenitale syfilitische- | osteochondropathie | vroege congenitale syfilitische- | pneumonie | vroege congenitale syfilitische- | rinitis | vroege congenitale syfilitische- | laryngitis




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Date index: 2023-11-22
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