Ophthalmology · Ophthalmology / Congenital malformation
Aniridia-Wilms tumor-genitourinary anomalies-retardation syndrome
also: WAGR syndrome
11p13 deletion syndrome with aniridia, Wilms tumor and intellectual disability.
- Specialty
- Ophthalmology
- Subspecialty
- Ophthalmology / Congenital malformation
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, congenital aniridia
- Gene(s) involved
- BDNF, PAX6, WT1
- Alternative names & eponyms
- WAGR syndrome
Etiology & mechanism
Contiguous deletion of PAX6 and WT1.
Gene(s) involved (3)
Symptoms & signs (6)
In plain terms, someone with Aniridia-Wilms tumor-genitourinary anomalies-retardation syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
4 shared
WAGR syndrome
aniridia, genitourinary anomalies, intellectual disability, wilms tumor
2 shared
Alström syndrome
nystagmus, obesity
2 shared
Börjeson–Forssman–Lehmann syndrome
intellectual disability, obesity
2 shared
Borjeson–Forssman–Lehmann syndrome
intellectual disability, obesity
2 shared
Prader–Willi syndrome
intellectual disability, obesity
2 shared
Schaaf–Yang syndrome
intellectual disability, obesity
1 shared
Acquired cerebellar syndrome
nystagmus
1 shared
Allan–Herndon–Dudley syndrome
intellectual disability
1 shared
Apert syndrome
intellectual disability
1 shared
Bardet–Biedl syndrome
obesity
Shares genes with
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