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Brachydactylia
Brachydactyly

Translation of "Brachydactyly " (English → French) :

brachydactyly
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
brachydactylie
Bones and Joints
Os et articulations
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
brachydactyly | brachydactylia
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
brachydactylie
médecine > anatomopathologie | biologie > embryologie
médecine > anatomopathologie | biologie > embryologie
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
brachydactyly
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
brachydactylie
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
This syndrome has characteristics of Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two mater
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de maladie de Hirschsprung-brachydactylie type D
SNOMEDCT-BE (type D brachydactyly). It has been described in four males from one family (two brothers and two mater / 721222007
SNOMEDCT-BE (disorder) / 721222007
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare genetic developmental defect during embryogenesis syndrome with characteristics of postaxial polydactyly and other abnormalities of the hands and feet (for example brachydactyly, broad toes), hypoplasia and fusion of the vertebral bodies, as w
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de polydactylie postaxiale-anomalies dentaires et vertébrales
SNOMEDCT-BE (for example brachydactyly, broad toes), hypoplasia and fusion of the vertebral bodies, as w / 773279006
SNOMEDCT-BE (disorder) / 773279006
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
brachydactylia | brachydactyly
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
brachydactilie | brachydactylie
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
A rare genetic syndromic intellectual disability with characteristics of mild intellectual disability, delayed speech development, congenital heart defects, brachydactyly and dysmorphic facial features.
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de microdélétion 14q24.1q24.3
SNOMEDCT-BE (disorder) / 773494008
SNOMEDCT-BE (disorder) / 773494008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


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'Brachydactyly'

Date index:2024-01-14 -

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