Rubinstein-Taybi, syndrome : arborescences MeSH
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Vous pouvez aussi consulter toutes les
arborescences
des mots clés utilisés dans CISMeF
appareil locomoteur, maladies
[C05]
os, maladies
[C05.116]
dysplasies os
[C05.116.099]
dysostoses
[C05.116.099.370]
dysostose crâniofaciale
[C05.116.099.370.231]
+
dysostoses orodigitofaciales
[C05.116.099.370.652]
hypoplasie dermique focale
[C05.116.099.370.380]
klippel-feil, syndrome
[C05.116.099.370.535]
Rubinstein-Taybi, syndrome
[C05.116.099.370.797]
synostose
[C05.116.099.370.894]
+
appareil locomoteur, maladies
[C05]
malformations appareil locomoteur
[C05.660]
malformations crâniofaciales
[C05.660.207]
crâniosynostose
[C05.660.207.240]
+
dysostose crâniofaciale
[C05.660.207.231]
+
dysostoses orodigitofaciales
[C05.660.207.700]
dysplasie cléidocranienne
[C05.660.207.207]
holoprosencéphalie
[C05.660.207.410]
malformations maxillofaciales
[C05.660.207.540]
+
microcéphalie
[C05.660.207.620]
Noonan, syndrome
[C05.660.207.690]
platybasie
[C05.660.207.720]
Rubinstein-Taybi, syndrome
[C05.660.207.850]
syndrome leopard
[C05.660.207.525]
système nerveux, maladies
[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]
Down, syndrome
[C10.597.606.643.220]
Prader Labhard Willi, syndrome
[C10.597.606.643.690]
retard mental lié à l'X
[C10.597.606.643.455]
+
Rubinstein-Taybi, syndrome
[C10.597.606.643.700]
WAGR, syndrome
[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]
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 et malformations congénitales, héréditaires et néonatales
[C16]
malformations
[C16.131]
anomalies chromosomiques
[C16.131.260]
Angelman, syndrome
[C16.131.260.040]
Beckwith Wiedemann, syndrome
[C16.131.260.080]
cri du chat, maladie
[C16.131.260.190]
De Lange, syndrome
[C16.131.260.210]
Down, syndrome
[C16.131.260.260]
holoprosencéphalie
[C16.131.260.380]
Prader Labhard Willi, syndrome
[C16.131.260.700]
Rubinstein-Taybi, syndrome
[C16.131.260.790]
syndrome branchio-oto-rénal
[C16.131.260.090]
troubles liés aberrations chromosomes sexuels
[C16.131.260.800]
+
WAGR, syndrome
[C16.131.260.940]
Williams, syndrome
[C16.131.260.970]
maladies et malformations congénitales, héréditaires et néonatales
[C16]
malformations
[C16.131]
malformations appareil locomoteur
[C16.131.621]
malformations crâniofaciales
[C16.131.621.207]
crâniosynostose
[C16.131.621.207.240]
+
dysostose crâniofaciale
[C16.131.621.207.231]
+
dysostoses orodigitofaciales
[C16.131.621.207.700]
dysplasie cléidocranienne
[C16.131.621.207.207]
holoprosencéphalie
[C16.131.621.207.410]
malformations maxillofaciales
[C16.131.621.207.540]
+
microcéphalie
[C16.131.621.207.620]
Noonan, syndrome
[C16.131.621.207.690]
platybasie
[C16.131.621.207.720]
Rubinstein-Taybi, syndrome
[C16.131.621.207.850]
syndrome leopard
[C16.131.621.207.525]
maladies et malformations congénitales, héréditaires et néonatales
[C16]
maladies génétiques congénitales
[C16.320]
anomalies chromosomiques
[C16.320.180]
Angelman, syndrome
[C16.320.180.040]
Beckwith Wiedemann, syndrome
[C16.320.180.080]
cri du chat, maladie
[C16.320.180.190]
De Lange, syndrome
[C16.320.180.210]
Down, syndrome
[C16.320.180.260]
holoprosencéphalie
[C16.320.180.380]
Prader Labhard Willi, syndrome
[C16.320.180.700]
Rubinstein-Taybi, syndrome
[C16.320.180.790]
syndrome branchio-oto-rénal
[C16.320.180.090]
troubles liés aberrations chromosomes sexuels
[C16.320.180.800]
+
WAGR, syndrome
[C16.320.180.940]
Williams, syndrome
[C16.320.180.970]
11 juin 2004
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© CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.
