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Acrochondrohyperplasia
Acromacria
Arachnodactily
Becker
Congenital mesodermal dystrophy
Dolichostenomelia
Dominant
Drug-induced
Dystrophia mesodermalis congenita
Dystrophia myotonica
Hyperchondroplasia
Isaacs
Marfan's abiotrophy
Marfan's dolichostenomely
Marfan's syndrome 1
Marfan-Achard syndrome
Myotonia chondrodystrophic
Myotonia congenita NOS
Neuromyotonia
Paramyotonia congenita Pseudomyotonia
Recessive
Spider fingers
Steinert
Streblodactyly
Symptomatic
Thomsen

Translation of "dystrophia mesodermalis congenita " (English → French) :

arachnodactily | Marfan's abiotrophy | Marfan's dolichostenomely | Marfan's syndrome 1 | Marfan-Achard syndrome | acrochondrohyperplasia | acromacria | congenital mesodermal dystrophy | dolichostenomelia | dystrophia mesodermalis congenita | hyperchondroplasia | spider fingers | streblodactyly

arachnodactylie | acromacrie | dolichosténomélie de Marfan | hyperchondroplasie | syndrome de Marfan
médecine > anatomopathologie | biologie > embryologie | biologie > génétique
médecine > anatomopathologie | biologie > embryologie | biologie > génétique


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

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




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'dystrophia mesodermalis congenita'

Date index:2021-03-10 -

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