Details of Disease | DrugMAP

General Information of Disease (ID: DIS2XL1O)

Disease Name	Neuroblastoma, susceptibility to, 1
Synonyms	susceptibility to neuroblastoma; neuroblastoma, susceptibility to; neuroblastoma, susceptibility to, 1, autosomal dominant, somatic mutation
Disease Hierarchy	DISGXLG5: Hereditary neoplastic syndrome DIS98MYE: Inherited disease susceptibility DIS2XL1O: Neuroblastoma, susceptibility to, 1
Disease Identifiers	MONDO ID MONDO_0009741 UMLS CUI C2749485 OMIM ID 256700 MedGen ID 412713

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
KIF1B	OTI1XQTO	Limited	Autosomal dominant	[1]
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References

1	Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.