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Anemie
Charcot-Marie-Tooth
Déjerine-Sottas
HMP-shuntbaan
Hereditair lymfoedeem
Hereditair lymfoedeem type 1
Hereditair lymfoedeem type 2
Infantiele hypertrofische-neuropathie
Syndroom van Roussy-Lévy
Ziekte van

Traduction de «Hereditair lymfoedeem type 1 » (Néerlandais → Anglais) :

hereditair lymfoedeem type 1
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Milroy lymphedema
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
hereditair lymfoedeem type 2
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Meige disease
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
hereditair lymfoedeem
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Hereditary lymphedema
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
hereditair lymfoedeem
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Hereditary lymphoedema
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
hereditaire motorische- en sensorische-neuropathie, type I-IV | infantiele hypertrofische-neuropathie | peroneale spieratrofie (axonaal type)(hypertrofisch type) | syndroom van Roussy-Lévy | ziekte van | Charcot-Marie-Tooth | ziekte van | Déjerine-Sottas
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
anemie (door) | enzymdeficiënties, behalve G-6-PD, verband houdend met hexosemonofosfaat-shuntbaan [HMP-shuntbaan] | anemie (door) | hemolytisch niet-sferocytair (hereditair), type I
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Anaemia (due to):enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway | haemolytic nonspherocytic (hereditary), type I
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]


D'autres ont cherché : charcot-marie-tooth     déjerine-sottas     hmp-shuntbaan     anemie     hemolytisch niet-sferocytair type     hereditair lymfoedeem     hereditair lymfoedeem type     peroneale spieratrofie     syndroom van roussy-lévy     ziekte     Hereditair lymfoedeem type 1     


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Date index: 2021-09-12
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