Angelman, syndrome : arborescences MeSH
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système nerveux, maladies
[C10]
système nerveux central, maladies
[C10.228]
troubles motricité
[C10.228.662]
Angelman, syndrome
[C10.228.662.075]
atrophie multisystémique
[C10.228.662.550]
+
dégénérescence hépatolenticulaire
[C10.228.662.425]
Hallervorden-Spatz, maladie
[C10.228.662.400]
paralysie supranucléaire progressive
[C10.228.662.700]
tic
[C10.228.662.825]
+
tremblement essentiel
[C10.228.662.350]
troubles choréiques
[C10.228.662.150]
+
troubles dystoniques
[C10.228.662.300]
+
troubles parkinsoniens
[C10.228.662.600]
+
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]
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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