Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
...
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Neoplastic Syndromes, Hereditary
Wilms Tumor
Endocrine System Diseases
Gonadal Disorders
Disorders of Sex Development
Disorder of Sex Development, 46,XY
...
Female Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
Disorder of Sex Development, 46,XY
...
Male Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
Disorder of Sex Development, 46,XY
...
Congenital Abnormalities
Urogenital Abnormalities
Disorders of Sex Development
Disorder of Sex Development, 46,XY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Eye Abnormalities
Aniridia
Término preferido
WAGR Syndrome
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Tipo
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mesh:Descriptor
Definición
- A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of WILMS TUMOR; ANIRIDIA; GENITOURINARY ABNORMALITIES; and INTELLECTUAL DISABILITY.
Concepto genérico
Etiquetas alternativas
- 11p Partial Monosomy Syndrome
- Chromosome 11p13 Deletion Syndrome
- Contiguous Gene Syndrome, WAGR
- WAGR Complex
- WAGR Contiguous Gene Syndrome
- Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome
- Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome
- Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome
- Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome
- Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome
En otras lenguas
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francés
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Syndrome associant tumeur de Wilms-aniridie-malformations génito-urinaires-retard mental
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Syndrome de délétion chromosomique 11p13
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Syndrome des gènes contigus WAGR
URI
http://data.loterre.fr/ark:/67375/JVR-MZCJWN7K-G
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