WAGR, syndrome : arborescences MeSH

[C04.557.435.595]

tumeur appareil urogénital

[C04.557.435.595.220]

WAGR, syndrome [C04.557.435.595.950]

[C04.588.945]

tumeur appareil urinaire

[C04.588.945.947]

tumeur rein

[C04.588.945.947.535]

[C04.588.945.947.535.585]

[C04.588.945.947.535.585.220]

WAGR, syndrome [C04.588.945.947.535.585.950]

tumeurs

[C04]

syndromes néoplasiques héréditaires

[C04.700]

[C04.700.635]

système nerveux, maladies

[C04.700.635.220]

WAGR, syndrome [C04.700.635.950]

[C10]

manifestations neurologiques

[C10.597]

manifestations neuro-comportementales

[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]

oeil, maladies

[C11]

malformations oculaires

[C11.250]

oeil, maladie héréditaire

[C11.250.060]

WAGR, syndrome [C11.250.060.950]

oeil, maladies

[C11]

[C11.270]

maladies urologiques et appareil génital mâle

[C11.270.060]

WAGR, syndrome [C11.270.060.950]

WAGR, syndrome [C11.941.375.060.950]

[C12]

malformations urogénitales

[C12.740]

[C12.740.700]

Alport, syndrome

[C12.740.700.742]

anomalie différenciation sexuelle

[C12.740.700.842]

cryptorchidie

[C12.740.700.258]

dysplasie rénale multikystique

rein polykystique, maladies

[C12.740.700.800]

WAGR, syndrome [C12.740.700.921]

maladies urologiques et appareil génital mâle

[C12]

tumeur appareil urogénital

[C12.740]

[C12.740.800]

tumeur appareil urinaire

[C12.740.800.820]

tumeur rein

[C12.740.800.820.750]

[C12.740.800.820.750.585]

[C12.740.800.820.750.585.220]

WAGR, syndrome [C12.740.800.820.750.585.950]

maladies urologiques et appareil génital mâle

[C12]

appareil urinaire, maladies

[C12.777.419.473.585]

[C12.777.419.473.585.220]

WAGR, syndrome [C12.777.419.473.585.950]

maladies appareil génital féminin et complications grossesse

[C13]

appareil génital féminin, maladies

[C13.371]

malformations urogénitales

[C13.371.820]

[C13.371.820.700]

Alport, syndrome

[C13.371.820.700.742]

anomalie différenciation sexuelle

[C13.371.820.700.842]

dysplasie rénale multikystique

[C13.371.820.700.558]

épispadias

[C13.371.820.700.374]

exstrophie vésicale

[C13.371.820.700.132]

rein polykystique, maladies

[C13.371.820.700.800]

WAGR, syndrome [C13.371.820.700.921]

maladies appareil génital féminin et complications grossesse

[C13]

appareil génital féminin, maladies

[C13.371]

tumeur appareil urogénital

[C13.371.820]

[C13.371.820.800]

tumeur appareil urinaire

[C13.371.820.800.820]

tumeur rein

[C13.371.820.800.820.535]

[C13.371.820.800.820.535.585]

[C13.371.820.800.820.535.585.220]

WAGR, syndrome [C13.371.820.800.820.535.585.950]

maladies et malformations congénitales, héréditaires et néonatales

Beckwith Wiedemann, syndrome

malformations

[C16.131]

anomalies chromosomiques

[C16.131.260]

Angelman, syndrome

[C16.131.260.040]

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

malformations

[C16.131]

malformations oculaires

[C16.131.384]

maladies et malformations congénitales, héréditaires et néonatales

[C16.131.384.079]

WAGR, syndrome [C16.131.384.079.950]

malformations urogénitales

malformations

[C16.131]

[C16.131.939]

Alport, syndrome

[C16.131.939.742]

anomalie différenciation sexuelle

[C16.131.939.842]

cryptorchidie

[C16.131.939.258]

dysplasie rénale multikystique

rein polykystique, maladies

[C16.131.939.800]

WAGR, syndrome [C16.131.939.921]

maladies et malformations congénitales, héréditaires et néonatales

maladies génétiques congénitales

[C16.320]

anomalies chromosomiques

[C16.320.180]

Angelman, syndrome

[C16.320.180.040]

Beckwith Wiedemann, syndrome

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]

maladies et malformations congénitales, héréditaires et néonatales

maladies génétiques congénitales

[C16.320]

oeil, maladie héréditaire

[C16.320.290]

maladies et malformations congénitales, héréditaires et néonatales

[C16.320.290.078]

WAGR, syndrome [C16.320.290.078.950]

maladies génétiques congénitales

[C16.320]

syndromes néoplasiques héréditaires

[C16.320.700]

[C16.320.700.642]