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Anomaly
Genetic anomalies of leukocytes
Genetic anomaly
Hereditary leukocytic hypersegmentation
Hyposegmentation
Leukomelanopathy
May-Hegglin
Pelger-Huët

Translation of "genetic anomalies leukocytes " (English → French) :

Genetic anomalies of leukocytes
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anomalies génétiques des leucocytes
WORLD HEALTH ORGANIZATION ICD-10: D72.0
WORLD HEALTH ORGANIZATION ICD-10: D72.0
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
genetic anomaly
https://www.termdat.bk.admin.c (...) (...) [HTML] [2018-01-01]
anomalie génétique
Medicine & biology
Biologie (Sciences médicales et biologiques)
https://www.termdat.bk.admin.c (...) (...) [HTML] [2018-01-01]
https://www.termdat.bk.admin.c (...) [HTML] [2018-01-01]
genetic anomaly
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
anomalie génétique
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 multiple congenital anomalies syndrome with characteristics of second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome branchio-otique
SNOMEDCT-BE (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing / 764810000
SNOMEDCT-BE (disorder) / 764810000
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anomalie (granulation) (granulocyte) ou syndrome de:Alder | May-Hegglin | Pelger-Huët | Hypersegmentation | Hyposegmentation | leucocytaire, héréditaire | Leucomélanopathie héréditaire
WORLD HEALTH ORGANIZATION ICD-10: D72.0
WORLD HEALTH ORGANIZATION ICD-10: D72.0
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
A rare genetic dysostosis disorder with characteristics of brachydactyly and other finger/toe anomalies (short and/or wide metacarpals, abnormal or absent metatarsals, broad halluces), carpal synostosis, fused cervical vertebrae, scoliosis and spina
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome d'acrodysplasie-scoliose
SNOMEDCT-BE (short and/or wide metacarpals, abnormal or absent metatarsals, broad halluces), carpal synostosis, fused cervical vertebrae, scoliosis and spina / 773773006
SNOMEDCT-BE (disorder) / 773773006
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome d'ataxie-photosensibilité-petite taille
SNOMEDCT-BE (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin / 773769008
SNOMEDCT-BE (disorder) / 773769008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Others have searched : anomaly or syndrome alder    genetic anomalies of leukocytes    may-hegglin    pelger-huët    genetic anomaly    hyposegmentation    leukomelanopathy    genetic anomalies leukocytes    


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'genetic anomalies leukocytes'

Date index:2022-10-18 -

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