Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/194072 http://purl.bioontology.org/ontology/OMIM/194072
Preferred Name	WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME
Synonyms	CHROMOSOME 11p13 DELETION SYNDROME WAGR SYNDROME WAGR WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATION SYNDROME
Type	http://www.w3.org/2002/07/owl#Class

altLabel	CHROMOSOME 11p13 DELETION SYNDROME WAGR SYNDROME WAGR WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATION SYNDROME
prefLabel	WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME
Gene Symbol	WAGR C11DELp13 DEL11p13
Scope Statement	Contiguous gene syndrome [MISCELLANEOUS] Caused by mutations in the Wilms tumor 1 gene (WT1, 607102.0001). [MOLECULAR BASIS] Caused by microdeletions of 11p13 [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU000623 http://purl.bioontology.org/ontology/OMIM/MTHU014918 http://purl.bioontology.org/ontology/OMIM/MTHU036365 http://purl.bioontology.org/ontology/OMIM/MTHU007655 http://purl.bioontology.org/ontology/OMIM/MTHU000133 http://purl.bioontology.org/ontology/OMIM/MTHU000066 http://purl.bioontology.org/ontology/OMIM/MTHU000250 http://purl.bioontology.org/ontology/OMIM/MTHU005880 See more See less
tui	T047
Gene Locus	11p13
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	194072
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018 http://purl.bioontology.org/ontology/OMIM/MTHU002860
cui	C0206115
Moved from	137357
OMIM Entry Type	3
OMIM MimType Value	pound

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