Details of Disease | DrugMAP

General Information of Disease (ID: DISQBKN1)

Disease Name	Wilms tumor 1
Synonyms	nephroblastoma; WT1; renal Wilms tumour; renal Wilms tumor; Wilms' tumor; Wilms' tumour; Wilms tumor, type 1, autosomal dominant, somatic mutation; Wilms tumor type 1; Wilms tumour type 1; Wilms tumor 1; Wilms tumor, somatic; Wilms tumor, autosomal dominant, somatic mutation
Disease Hierarchy	DISYBXFF: Hereditary Wilms tumor DISQBKN1: Wilms tumor 1

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
WT1	OTP7KC3D	Definitive	Autosomal dominant	[1]
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This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
WT1	TTZ8UT4	Definitive	Autosomal dominant	[1]
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References

1	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.