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

Vertaling van "genetic anomalies leukocytes " (Engels → Nederlands) :

Genetic anomalies of leukocytes
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
genetische anomalieën van leukocyten
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
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]
branchio-otisch syndroom
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare genetic multiple developmental anomalies syndrome with characteristics of craniofacial anomalies (microcephaly, brachycephaly, craniosynostosis, facial asymmetry, cleft lip, cleft palate, dysmorphic facial features, ear lobe malformations, low
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Pilotto-syndroom
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 (granulatie)(granulocyt) of syndroom van | Alder | anomalie (granulatie)(granulocyt) of syndroom van | May-Hegglin | anomalie (granulatie)(granulocyt) of syndroom van | Pelger-Huët | hereditaire | leukocytaire | hypersegmentatie | hereditaire | leukocytaire | hyposegmentatie | hereditaire | leukomelanopathie
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [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]
syndroom van Fenton-Wilkinson-Toselano
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : anomaly or syndrome alder     genetic anomalies of leukocytes     may-hegglin     pelger-huët     hyposegmentation     leukomelanopathy     genetic anomalies leukocytes     


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Date index: 2023-08-22
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