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Becker
Chondrodystrofisch
Dominant
Door geneesmiddelen
Dystrophia myotonica
Fragilitas ossium
Isaacs
Myotonia acquisita
Myotonia atrophica
Myotonia congenita
Myotonia congenita type Thomsen
Myotonia fluctuans
Myotonia hereditaria
Myotonia permanens
Myotonie
NNO
Neuromyotonie
Osteopsathyrose
Paramyotonia congenita
Pramyotonia congenita
Pseudomyotonie
Recessief
Steinert
Symptomatisch
Syndroom van Curschmann-Steinert
Thomsen
Ziekte van Deleage
Ziekte van Talma
Ziekte van Thomsen

Traduction de «Myotonia hereditaria » (Néerlandais → Anglais) :

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

congenital myotonia | hereditary myotonia | Thomsen disease


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

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


dystrophia myotonica | myotonia atrophica | syndroom van Curschmann-Steinert | ziekte van Deleage

Curschmann-Batten-Steinert syndrome | Curschmann-Steinert syndrome








myotonia congenita type Thomsen

Myotonia congenita - autosomal dominant form


fragilitas ossium (hereditaria) | osteopsathyrose

Fragilitas ossium Osteopsathyrosis




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Date index: 2020-12-20
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