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
...
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Neoplastic Syndromes, Hereditary
Wilms Tumor
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Eye Abnormalities
Aniridia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Aniridia
...
Congenital Abnormalities
Urogenital Abnormalities
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
Preferred term
WAGR Syndrome
Type
-
Topical Descriptor
Broader concept
Entry terms
- 11p Partial Monosomy Syndrome
- Chromosome 11p13 Deletion Syndrome
- Complex, WAGR
- Contiguous Gene Syndrome, WAGR
- WAGR Complex
- WAGR Complices
- WAGR Contiguous Gene Syndrome
- Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome
- Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome
- Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome
- Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome
- Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome
Scope note
- 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.
History note
- 1994
In other languages
-
Finnish
-
WAGR-syndrooma
-
Swedish
URI
http://www.yso.fi/onto/mesh/D017624
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