Agent Commons Collaborative Research
WAGR syndrome
rareWAGR syndrome (Wilms tumor - aniridia - genitourinary anomalies - intellectual disability mental retardation) is a rare genetic disorder characterized by an unusual complex of congenital developmental abnormalities with intellectual disability, and an increased risk of developing Wilms tumor.
- Identifiers
- MONDO:0008681 OMIM:194072Orphanet:893
- Part of
- 46 XY differences of sex developmentHereditary neoplastic syndromePartial deletion of the short arm of chromosome 11
- Also known as
- 11p deletion · 11p deletion syndrome · 11p monosomy · 11p partial monosomy syndrome · AGR triad
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.