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Denny-Brown
Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie sensitive
Récessive
Syndrome de Nélaton

Translation of "morvan neuropathie sensitive " (French → English) :

Maladie de Morvan Neuropathie sensitive héréditaire à transmission:dominante | récessive | Syndrome de Nélaton
https://icd.who.int/browse10/2 (...) (...) [HTML]
Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited
WORLD HEALTH ORGANIZATION ICD-10: G60.8
WORLD HEALTH ORGANIZATION ICD-10: G60.8
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
neuropathie sensitive congénitale avec perte sélective des petites fibres myélinisées
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Hereditary sensory and autonomic neuropathy type V
SNOMEDCT-CA (trouble) / 128206006
SNOMEDCT-CA (trouble) / 128206006
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https://browser.ihtsdotools.or (...) [HTML]
neuropathie sensitive
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Sensory neuropathy
SNOMEDCT-BE (disorder) / 95662005
SNOMEDCT-BE (disorder) / 95662005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Neuromyopathie carcinomateuse (C00-C97+) Neuropathie sensitive paranéoplasique [Denny-Brown] (C00-D48+)
https://icd.who.int/browse10/2 (...) (...) [HTML]
Carcinomatous neuromyopathy (C00-C97+) Sensorial paraneoplastic neuropathy [Denny Brown] (C00-D48+)
WORLD HEALTH ORGANIZATION ICD-10: G13.0*
WORLD HEALTH ORGANIZATION ICD-10: G13.0*
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [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]
neuropathie héréditaire sensitive et autonomique avec surdité et retard de développement
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This syndrome has characteristics of sensory and autonomic axonal neuropathy, sensorineural hearing loss and persistent global developmental delay. It has been described in four individuals from a consanguineous Lebanese family. Onset occurred in inf
SNOMEDCT-BE (disorder) / 717826009
SNOMEDCT-BE (disorder) / 717826009
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https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1B
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Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008
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]


Others have searched : denny-brown    syndrome de nélaton    neuropathie héréditaire sensitive et autonomique    neuropathie sensitive    récessive    morvan neuropathie sensitive    


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morvan neuropathie sensitive

Date index:2021-05-20 -

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