Mobius, syndrome : arborescences MeSH
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Vous pouvez aussi consulter toutes les
arborescences
des mots clés utilisés dans CISMeF
système nerveux, maladies
[C10]
nerfs crâniens, maladies
[C10.292]
nerf facial, maladies
[C10.292.300]
algie faciale
[C10.292.300.625]
Bell, maladie
[C10.292.300.250]
hémiatrophie faciale
[C10.292.300.375]
melkersson-rosenthal, syndrome
[C10.292.300.800]
Mobius, syndrome
[C10.292.300.825]
traumatisme nerf facial
[C10.292.300.500]
zona otitique
[C10.292.300.750]
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 et malformations congénitales, héréditaires et néonatales
[C16]
nouveau-né, maladies
[C16.614]
anémie néonatale
[C16.614.053]
+
asphyxie néonatale
[C16.614.092]
bandes amniotiques, syndrome
[C16.614.042]
conjonctivite gonococcique nouveau-né
[C16.614.677]
déficit immunitaire combiné sévère
[C16.614.815]
épilepsie bénigne néonatale
[C16.614.258]
érythroblastose foetale
[C16.614.304]
+
hernie ombilicale
[C16.614.390]
hydrocéphalie
[C16.614.414]
+
hydrophtalmie
[C16.614.438]
hyperostose corticale infantile
[C16.614.465]
hypoglycémie hyperinsulinique persistante du nourrisson
[C16.614.716]
ichtyose
[C16.614.492]
+
ictère néonatal
[C16.614.555]
+
inhalation méconium
[C16.614.580]
Mobius, syndrome
[C16.614.595]
mucoviscidose
[C16.614.213]
nanisme thanatophore
[C16.614.890]
nouveau-né, maladie hémorragique
[C16.614.378]
nystagmus congénital
[C16.614.643]
persistance circulation foetale
[C16.614.694]
poïkilodermie congénitale
[C16.614.739]
prématuré, maladies
[C16.614.521]
+
sclérème nouveau-né
[C16.614.810]
sevrage néonatal, syndrome
[C16.614.610]
syphilis congénitale
[C16.614.868]
toxoplasmose congénitale
[C16.614.909]
traumatisme obstétrical
[C16.614.131]
+
Wolman, maladie
[C16.614.947]
11 juin 2004
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