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Elliptocytose familiale
Elliptocytose héréditaire
Fibromatose gingivale héréditaire
Hypersegmentation
Hyposegmentation
Leucomélanopathie héréditaire
May-Hegglin
Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Paralysie faciale congénitale héréditaire isolée
Paralysie spastique infantile ascendante héréditaire
Pelger-Huët

Translation of "elliptocytose héréditaire " (French → English) :

Elliptocytose héréditaire
https://icd.who.int/browse10/2 (...) (...) [HTML]
Hereditary elliptocytosis
WORLD HEALTH ORGANIZATION ICD-10: D58.1
WORLD HEALTH ORGANIZATION ICD-10: D58.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Elliptocytose (congénitale) Ovalocytose (congénitale) (héréditaire)
https://icd.who.int/browse10/2 (...) (...) [HTML]
Elliptocytosis (congenital) Ovalocytosis (congenital)(hereditary)
WORLD HEALTH ORGANIZATION ICD-10: D58.1
WORLD HEALTH ORGANIZATION ICD-10: D58.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
elliptocytose familiale
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary ovalocytosis
SNOMEDCT-BE (disorder) / 191169008
SNOMEDCT-BE (disorder) / 191169008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Anomalie (granulation) (granulocyte) ou syndrome de:Alder | May-Hegglin | Pelger-Huët | Hypersegmentation | Hyposegmentation | leucocytaire, héréditaire | Leucomélanopathie héréditaire
https://icd.who.int/browse10/2 (...) (...) [HTML]
Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy
WORLD HEALTH ORGANIZATION ICD-10: D72.0
WORLD HEALTH ORGANIZATION ICD-10: D72.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
paralysie faciale congénitale héréditaire isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or a
SNOMEDCT-BE (disorder) / 733091002
SNOMEDCT-BE (disorder) / 733091002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire de l'adulte jeune
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005
SNOMEDCT-BE (disorder) / 128205005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
fibromatose gingivale héréditaire
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary gingival fibromatosis
SNOMEDCT-BE (disorder) / 109620006
SNOMEDCT-BE (disorder) / 109620006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
paralysie spastique infantile ascendante héréditaire
https://browser.ihtsdotools.or (...) (...) [HTML]
IAHSP - infantile onset ascending hereditary spastic paralysis
SNOMEDCT-BE (disorder) / 703543005
SNOMEDCT-BE (disorder) / 703543005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : elliptocytose ovalocytose    elliptocytose héréditaire    hypersegmentation    hyposegmentation    leucomélanopathie héréditaire    may-hegglin    pelger-huët    elliptocytose familiale    fibromatose gingivale héréditaire    leucocytaire héréditaire    neuropathie héréditaire sensitive et autonomique    paralysie faciale congénitale héréditaire isolée    paralysie spastique infantile ascendante héréditaire    


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elliptocytose héréditaire

Date index:2021-07-27 -

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