Alagille, syndrome : arborescences MeSH
Vous pouvez aussi consulter toutes les
arborescences
des mots clés utilisés dans CISMeF
maladie de l'appareil digestif
[C06]
voies biliaires, maladies
[C06.130]
canaux biliaires, maladies
[C06.130.120]
cholestase
[C06.130.120.135]
cholestase intra-hépatique
[C06.130.120.135.250]
Alagille, syndrome
[C06.130.120.135.250.125]
cirrhose biliaire
[C06.130.120.135.250.250]
maladie de l'appareil digestif
[C06]
foie, maladies
[C06.552]
cholestase intra-hépatique
[C06.552.150]
Alagille, syndrome
[C06.552.150.125]
cirrhose biliaire
[C06.552.150.250]
maladies cardiovasculaires
[C14]
malformations cardiovasculaires
[C14.240]
cardiopathies congénitales
[C14.240.400]
Alagille, syndrome
[C14.240.400.044]
anomalies des vaisseaux coronaires
[C14.240.400.210]
atrésie tricuspidienne
[C14.240.400.920]
coarctation aortique
[C14.240.400.090]
coeur croisé
[C14.240.400.220]
coeur triatrial
[C14.240.400.200]
communications intercavitaires cardiaques
[C14.240.400.560]
+
complexe d'Eisenmenger
[C14.240.400.450]
dextrocardie
[C14.240.400.280]
+
dysplasie ventriculaire droite arythmogène
[C14.240.400.145]
hypoplasie coeur gauche, syndrome
[C14.240.400.625]
levocardie
[C14.240.400.701]
maladie d'Ebstein
[C14.240.400.395]
persistance du canal artériel
[C14.240.400.340]
syndrome de Marfan
[C14.240.400.725]
syndrome LEOPARD
[C14.240.400.695]
tétralogie de Fallot
[C14.240.400.849]
transposition des gros vaisseaux
[C14.240.400.915]
+
tronc artériel commun
[C14.240.400.929]
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]
28 septembre 2005
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