Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/194071 http://purl.bioontology.org/ontology/OMIM/194071
Preferred Name	WILMS TUMOR 2
Synonyms	WT2
Type	http://www.w3.org/2002/07/owl#Class

altLabel	WT2
prefLabel	WILMS TUMOR 2
Gene Symbol	BWS SRS1 ICR1 WT2
Scope Statement	Caused by mutation in the H19-IGF2-imprinting control region gene (ICR1, 616186.0002) [MOLECULAR BASIS] Most case are sporadic [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU005880
tui	T047
Gene Locus	11p15.5
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	194071
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	C3887743
OMIM Entry Type	3
OMIM MimType Value	pound

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