A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of Wilms' tumor (W), ANIRIDIA (A), genitourinary abnormalities (G), and mental retardation (R).
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Provides an overview of this unusual complex of congenital developmental abnormalities which include aniridia, genitourinary malformations and mental retardation.
Information on this rare genetic condition, its diagnosis, treatment and inheritance, provided by the National Human Genome Research Institute.
Offers the synonyms, a general discussion and further resources.
Information for families or physicians interested in learning more about WAGR Syndrome.
Offers the synonyms, a general discussion and further resources.
Provides an overview of this unusual complex of congenital developmental abnormalities which include aniridia, genitourinary malformations and mental retardation.
Information on this rare genetic condition, its diagnosis, treatment and inheritance, provided by the National Human Genome Research Institute.
Information for families or physicians interested in learning more about WAGR Syndrome.
Last update:
March 5, 2021 at 6:15:09 UTC
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- Recently edited by merlin1
- Recently edited by merlin1