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Becker
Bessel-Hagen disease
Congenital myotonia
Diagnosis and management of hereditary disorders
Dominant
Drug-induced
Dystrophia myotonica
Hereditary deforming chondrodysplasia
Hereditary disposition
Hereditary multiple exostosis
Hereditary myotonia
Hereditary predisposition
Isaacs
Medical genetics
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas
Myotonia chondrodystrophic
Myotonia congenita - autosomal dominant form
Myotonia congenita NOS
Myotonia permanens
Neuromyotonia
Paramyotonia congenita Pseudomyotonia
Recessive
Steinert
Symptomatic
Thomsen
Thomsen disease

Vertaling van "Hereditary myotonia " (Engels → Nederlands) :

congenital myotonia | hereditary myotonia | Thomsen disease

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


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


Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas

heriditaire multiple exostose | multiple erfelijk osteochondroom | HME [Abbr.]


hereditary disposition | hereditary predisposition

erfelijke aanleg


Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec

erfelijke plaatsspecifieke eierstokkanker-syndroom




Myotonia congenita - autosomal dominant form

congenitale myotonie, autosomale dominante vorm


diagnosis and management of hereditary disorders | medical genetics

medische genetica


Adenomatosis of colon Large intestine NOS Polyposis (hereditary) of colon

adenomatose van colon | dikke darm NNO | polypose (hereditair) van colon


Imerslund(-Gräsbeck) syndrome Megaloblastic hereditary anaemia

megaloblastaire hereditaire-anemie | syndroom van Imerslund(-Gräsbeck)




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Date index: 2024-03-13
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