disease has feature
Aniridia
Intellectual disability
WAGR syndrome
https://github.com/monarch-initiative/mondo/issues/4521
https://github.com/monarch-initiative/mondo/issues/6744
https://github.com/monarch-initiative/mondo/issues/6753
https://rarediseases.info.nih.gov/diseases/5528/wagr-syndrome
Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
WAGR 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.
Wilms tumor-aniridia-gonadoblastoma-mental retardation syndrome
chromosome 11p deletion
UMLS:C0206115
deletion 11p
SCTID:715215007
chromosome 11P13 deletion syndrome
chromosome 11p deletion syndrome
chromosome 11p13 deletion syndrome
MONDO:0008681
WAGR 11p13 deletion syndrome
NORD:1833
Del(11)(p13)
DOID:14515
Wilms tumor, aniridia, genitourinary anomalies, and intellectual disability syndrome
11p monosomy
AGR triad
MESH:D017624
NCIT:C3718
Wilms tumor, aniridia, genitourinary anomalies, intellectual disability syndrome
WAGR syndrome
monosomy 11p13
11p deletion syndrome
partial monosomy 11p
WAGR
11p partial monosomy syndrome
Orphanet:893
Wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome
Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome
OMIM:194072
deletion 11p13
Wilms tumor-aniridia-gonadoblastoma-intellectual disability syndrome
11p deletion
Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome, autosomal dominant, somatic mutation
GARD:5528
WAGR Complex
Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome
Wilms tumor, aniridia, genitourinary anomalies and developmental delay syndrome
monosomy 11p
DECIPHER:35
hereditary neoplastic syndrome
partial deletion of the short arm of chromosome 11
46,XY disorder of sex development