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Achard-Foix-Mouzon syndrome
Acrochondrohyperplasia
Acromacria
Arachnodactily
Congenital mesodermal dystrophy
Dolichostenomelia
Dystrophia mesodermalis congenita
Hyperchondroplasia
Marfan syndrome
Marfan's abiotrophy
Marfan's dolichostenomely
Marfan's syndrome
Marfan's syndrome 1
Marfan-Achard syndrome
Neonatal Marfan syndrome
Spider fingers
Streblodactyly

Translation of "Marfan-Achard syndrome " (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
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
arachnodactylie | acromacrie | dolichosténomélie de Marfan | hyperchondroplasie | syndrome de Marfan
médecine > anatomopathologie | biologie > embryologie | biologie > génétique
médecine > anatomopathologie | biologie > embryologie | biologie > génétique
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
Marfan syndrome | Marfan's syndrome
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
syndrome de Marfan
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Marfan's syndrome
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Syndrome de Marfan
WORLD HEALTH ORGANIZATION ICD-10: Q87.4
WORLD HEALTH ORGANIZATION ICD-10: Q87.4
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Achard-Foix-Mouzon syndrome
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
syndrome d'Achard-Foix-Mouzon
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
A rare severe and life-threatening genetic disease occurring during the neonatal period. The disease has characteristics of classical Marfan syndrome manifestations in addition to facial dysmorphism (megalocornea, iridodonesis, ectopia lentis, crumpl
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de Marfan néonatal
SNOMEDCT-BE (megalocornea, iridodonesis, ectopia lentis, crumpl / 763839005
SNOMEDCT-BE (disorder) / 763839005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Neonatal Marfan syndrome
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
MFS néonatal
SNOMEDCT-BE (megalocornea, iridodonesis, ectopia lentis, crumpl / 763839005
SNOMEDCT-BE (disorder) / 763839005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Others have searched : achard-foix-mouzon syndrome    marfan syndrome    marfan's abiotrophy    marfan's dolichostenomely    marfan's syndrome    marfan-achard syndrome    neonatal marfan syndrome    acromacria    arachnodactily    congenital mesodermal dystrophy    dolichostenomelia    dystrophia mesodermalis congenita    hyperchondroplasia    spider fingers    streblodactyly    Marfan-Achard syndrome    


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'Marfan-Achard syndrome'

Date index:2021-09-08 -

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