De lange, syndrome : arborescences MeSH
Vous pouvez aussi consulter toutes les
arborescences
des mots clés utilisés dans CISMeF
maladies du système nerveux
[C10]
manifestations neurologiques
[C10.597]
manifestations neuro-comportementales
[C10.597.606]
retard mental
[C10.597.606.643]
cri du chat, maladie
[C10.597.606.643.180]
De Lange, syndrome
[C10.597.606.643.210]
Prader Labhard Willi, syndrome
[C10.597.606.643.690]
retard mental lié à l'X
[C10.597.606.643.455]
+
syndrome de Down
[C10.597.606.643.220]
syndrome de Rubinstein-Taybi
[C10.597.606.643.700]
syndrome WAGR
[C10.597.606.643.969]
Williams, syndrome
[C10.597.606.643.970]
maladies et malformations congénitales, héréditaires et néonatales
[C16]
malformations
[C16.131]
malformations multiples
[C16.131.077]
Alagille, syndrome
[C16.131.077.065]
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]
dysostoses orodigitofaciales
[C16.131.077.677]
dysplasie ectodermique
[C16.131.077.350]
+
holoprosencéphalie
[C16.131.077.410]
incontinentia pigmenti
[C16.131.077.445]
Laurence-Moon, syndrome
[C16.131.077.509]
Lowe, syndrome
[C16.131.077.661]
naevomatose basocellulaire
[C16.131.077.130]
ostéoonychodysostose
[C16.131.077.606]
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]
syndrome branchio-oto-rénal
[C16.131.077.208]
syndrome d'Angelman
[C16.131.077.095]
syndrome de Bardet-Biedl
[C16.131.077.112]
syndrome de Down
[C16.131.077.327]
syndrome de Gardner
[C16.131.077.393]
syndrome de Marfan
[C16.131.077.550]
syndrome de Mobius
[C16.131.077.578]
syndrome de Protée
[C16.131.077.740]
syndrome de Rubinstein-Taybi
[C16.131.077.804]
syndrome de Smith-Lemli-Optiz
[C16.131.077.860]
syndrome de Waardenburg
[C16.131.077.938]
syndrome de Zellweger
[C16.131.077.970]
syndrome LEOPARD
[C16.131.077.525]
syndrome POEMS
[C16.131.077.703]
Wolfram, syndrome
[C16.131.077.951]
maladies et malformations congénitales, héréditaires et néonatales
[C16]
malformations
[C16.131]
anomalies chromosomiques
[C16.131.260]
Beckwith Wiedemann, syndrome
[C16.131.260.080]
CADASIL
[C16.131.260.140]
cri du chat, maladie
[C16.131.260.190]
De Lange, syndrome
[C16.131.260.210]
holoprosencéphalie
[C16.131.260.380]
Prader Labhard Willi, syndrome
[C16.131.260.700]
syndrome branchio-oto-rénal
[C16.131.260.090]
syndrome d'Angelman
[C16.131.260.040]
syndrome de Down
[C16.131.260.260]
syndrome de Rubinstein-Taybi
[C16.131.260.790]
syndrome WAGR
[C16.131.260.940]
troubles liés aberrations chromosomes sexuels
[C16.131.260.800]
+
Williams, syndrome
[C16.131.260.970]
maladies et malformations congénitales, héréditaires et néonatales
[C16]
maladies génétiques congénitales
[C16.320]
anomalies chromosomiques
[C16.320.180]
Beckwith Wiedemann, syndrome
[C16.320.180.080]
CADASIL
[C16.320.180.140]
cri du chat, maladie
[C16.320.180.190]
De Lange, syndrome
[C16.320.180.210]
holoprosencéphalie
[C16.320.180.380]
Prader Labhard Willi, syndrome
[C16.320.180.700]
syndrome branchio-oto-rénal
[C16.320.180.090]
syndrome d'Angelman
[C16.320.180.040]
syndrome de Down
[C16.320.180.260]
syndrome de Rubinstein-Taybi
[C16.320.180.790]
syndrome WAGR
[C16.320.180.940]
troubles liés aberrations chromosomes sexuels
[C16.320.180.800]
+
Williams, syndrome
[C16.320.180.970]
14 septembre 2005
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