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Alport's syndrome
Amelogenesis imperfecta
Becker
Bessel-Hagen disease
Congenital myotonia
Dominant
Drug-induced
Dystrophia myotonica
Familial hereditary nephropathy
Fibromatosis gingivae
Friedreich disease
Friedreich familial ataxia
Friedreich hereditary ataxia
Friedreich hereditary spinal ataxia
Friedreich spinocerebella
Friedreich's ataxia
Friedreich's disease
Friedreich's familial ataxia
Friedreich's hereditary ataxia
Friedreich's hereditary spinal ataxia
Haematuric familial nephropathy
Hereditary amelogenesis imperfecta
Hereditary deforming chondrodysplasia
Hereditary disposition
Hereditary enamel dysplasia
Hereditary enemy
Hereditary foe
Hereditary gingival fibromatosis
Hereditary hyperplasia of the gingiva
Hereditary multiple exostosis
Hereditary myotonia
Hereditary nephropathy
Hereditary nephropathy with haematuria
Hereditary predisposition
Isaacs
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas
Myotonia chondrodystrophic
Myotonia congenita
Myotonia congenita NOS
Neuromyotonia
Paramyotonia congenita Pseudomyotonia
Recessive
Steinert
Symptomatic
Thomsen
Thomsen disease
Thomsen's disease

Translation of "Hereditary myotonia " (English → French) :

congenital myotonia | hereditary myotonia | Thomsen disease
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
maladie de Thomsen | myotonic congénitale
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
hereditary nephropathy | Alport's syndrome | hereditary haematuria associated with nerve deafness and ocular changes | hereditary hematuria associated with nerve deafness and ocular changes | hereditary nephropathy with haematuria | familial hereditary nephropathy | haematuric familial nephropathy
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
néphropathie familiale avec surdité | syndrome d'Alport | néphrite hématurique héréditaire avec surdité | néphrite chronique héréditaire
médecine > néphrologie et urologie
médecine > néphrologie et urologie
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
Friedreich's ataxia [ Friedreich's disease | Friedreich disease | Friedreich's hereditary spinal ataxia | Friedreich hereditary spinal ataxia | Friedreich familial ataxia | Friedreich's familial ataxia | Friedreich hereditary ataxia | Friedreich's hereditary ataxia | Friedreich spinocerebella ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
ataxie de Friedreich [ maladie de Friedreich | ataxie héréditaire ]
Nervous System
Système nerveux
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
myotonia congenita [ Thomsen's disease | congenital myotonia ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
maladie de Thomsen [ myotonie congénitale ]
Musculoskeletal System | Special Education
Appareil locomoteur (Médecine) | Éducation spéciale
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
hereditary hyperplasia of the gingiva | hereditary gingival fibromatosis | fibromatosis gingivae
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
hyperplasie gingivale congénitale diffuse | fibromatose idiopathique | éléphantiasis gingival | hyperplasie gingivale idiopathique
médecine > pathologie dentaire
médecine > pathologie dentaire
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
hereditary enamel dysplasia | amelogenesis imperfecta | hereditary amelogenesis imperfecta
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
dystrophie brune héréditaire de l'émail | amélogenèse imparfaite | hypoplasie brune héréditaire de l'émail
médecine > pathologie dentaire
médecine > pathologie dentaire
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
Dystrophia myotonica [Steinert] Myotonia:chondrodystrophic | drug-induced | symptomatic | Myotonia congenita:NOS | dominant [Thomsen] | recessive [Becker] | Neuromyotonia [Isaacs] Paramyotonia congenita Pseudomyotonia
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Dystrophie myotonique [Steinert] Myotonie:chondrodystrophique | congénitale:SAI | dominante [Thomsen] | récessive [Becker] | médicamenteuse | symptomatique | Neuromyotonie [Isaacs] Paramyotonie congénitale Pseudomyotonie
WORLD HEALTH ORGANIZATION ICD-10: G71.1
WORLD HEALTH ORGANIZATION ICD-10: G71.1
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
hereditary foe [ hereditary enemy ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
ennemi héréditaire
International Relations
Relations internationales
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
chondrodysplasie déformante héréditaire | maladie de Bessel-Hagen | maladie des exostoses multiples | maladie exostosante | maladie ostéogénique | ostéochondromes multiples
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
hereditary disposition | hereditary predisposition
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
disposition héréditaire | prédisposition héréditaire
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]


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'Hereditary myotonia'

Date index:2021-09-05 -

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