POEMS, syndrome : arborescences MeSH
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Vous pouvez aussi consulter toutes les
arborescences
des mots clés utilisés dans CISMeF
système nerveux, maladies
[C10]
appareil neuromusculaire, maladies
[C10.668]
système nerveux périphérique, maladies
[C10.668.829]
polynévrites
[C10.668.829.800]
neuropathie alcoolique
[C10.668.829.800.050]
neuropathies héréditaires autonomes et sensorielles
[C10.668.829.800.625]
+
neuropathies héréditaires motrices et sensorielles
[C10.668.829.800.300]
+
POEMS, syndrome
[C10.668.829.800.700]
polynévrite paranéoplasique
[C10.668.829.800.662]
polyradiculonévrite
[C10.668.829.800.750]
+
Tangier, maladie
[C10.668.829.800.875]
hémopathies et maladies lymphatiques
[C15]
hémopathies
[C15.378]
anomalie protéine sang
[C15.378.147]
paraprotéinémies
[C15.378.147.780]
chaînes lourdes, maladie
[C15.378.147.780.490]
+
cryoglobulinémie
[C15.378.147.780.243]
macroglobulinémie
[C15.378.147.780.925]
myélome multiple
[C15.378.147.780.650]
POEMS, syndrome
[C15.378.147.780.750]
maladies et malformations congénitales, héréditaires et néonatales
[C16]
malformations
[C16.131]
malformations multiples
[C16.131.077]
Alagille, syndrome
[C16.131.077.065]
Angelman, syndrome
[C16.131.077.095]
Bardet-Biedl, syndrome
[C16.131.077.112]
Beckwith Wiedemann, syndrome
[C16.131.077.133]
Bloom, syndrome
[C16.131.077.137]
Cockayne, syndrome
[C16.131.077.250]
cri du chat, maladie
[C16.131.077.262]
De Lange, syndrome
[C16.131.077.272]
Down, syndrome
[C16.131.077.327]
dysostoses orodigitofaciales
[C16.131.077.677]
dysplasie ectodermique
[C16.131.077.350]
+
Gardner, syndrome
[C16.131.077.393]
holoprosencéphalie
[C16.131.077.410]
incontinentia pigmenti
[C16.131.077.445]
Laurence-Moon, syndrome
[C16.131.077.509]
Lowe, syndrome
[C16.131.077.661]
Marfan, syndrome
[C16.131.077.550]
Mobius, syndrome
[C16.131.077.578]
naevomatose basocellulaire
[C16.131.077.130]
ostéoonychodysostose
[C16.131.077.606]
POEMS, syndrome
[C16.131.077.703]
polydactylie côte courte, syndrome
[C16.131.077.850]
Prader Labhard Willi, syndrome
[C16.131.077.730]
Prune Belly, syndrome
[C16.131.077.745]
rubéole congénitale
[C16.131.077.790]
Rubinstein-Taybi, syndrome
[C16.131.077.804]
Smith-Lemli-Opitz, syndrome
[C16.131.077.860]
syndrome branchio-oto-rénal
[C16.131.077.208]
syndrome de protée
[C16.131.077.740]
syndrome leopard
[C16.131.077.525]
Waardenburg, syndrome
[C16.131.077.938]
Wolfram, syndrome
[C16.131.077.951]
Zellweger, syndrome
[C16.131.077.970]
maladies immunologiques
[C20]
troubles immunoprolifératifs
[C20.683]
paraprotéinémies
[C20.683.780]
chaînes lourdes, maladie
[C20.683.780.490]
+
cryoglobulinémie
[C20.683.780.250]
gammapathie monoclonale bénigne
[C20.683.780.640]
+
macroglobulinémie
[C20.683.780.925]
myélome multiple
[C20.683.780.650]
POEMS, syndrome
[C20.683.780.750]
11 juin 2004
courriel
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© CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.
