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Vertaling van "deep thrombophlebitis " (Engels → Nederlands) :

Deep thrombophlebitis

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

diepe tromboflebitis

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Phlebitis and thrombophlebitis of other deep vessels of lower extremities

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

flebitis en tromboflebitis van overige diepe venen van onderste extremiteiten

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

Deep-vein thrombosis, postpartum Pelvic thrombophlebitis, postpartum

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

diepe veneuze-trombosepost partum | tromboflebitis in bekkenpost partum

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

deep-frozen product [ deep-frozen food | deep-frozen foodstuff ]

http://eurovoc.europa.eu/drupa (...) (...) [HTML] [2017-12-31]

diepvriesproduct [ diepgevroren levensmiddel | diepvriesprodukt ]

http://eurovoc.europa.eu/drupa (...) (...) [HTML] [2017-12-31]

http://eurovoc.europa.eu/drupa (...) [HTML] [2017-12-31]

use deep tissue massage | utilise deep tissue massage | apply deep tissue massage | practice deep tissue massage

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

diepe massage toepassen | deep tissue massage toepassen | diepeweefselmassage toepassen

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]

A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are intellectual disability, growth and developmental delay, facial dysmorphism (including microphthalmia, deep-set eyes, low-set, malformed ears, bulbous

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

mozaïektrisomie 9

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A rare hereditary motor and sensory neuropathy disorder with characteristics of the typical CMT phenotype (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type F

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

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