Details of Disease

General Information of Disease (ID: DISPD991)

Disease Name Neuroblastoma, susceptibility to, 2
Synonyms susceptibility to neuroblastoma 2; neuroblastoma, susceptibility to, type 2; NBLST2
Disease Hierarchy
DISGXLG5: Hereditary neoplastic syndrome
DIS98MYE: Inherited disease susceptibility
DISPD991: Neuroblastoma, susceptibility to, 2
Disease Identifiers
MONDO ID
MONDO_0700041
UMLS CUI
C2751682
OMIM ID
613013
MedGen ID
416607

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
PHOX2B OT3SFR2O Definitive Autosomal dominant [1]
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References

1 Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13. Cancer Res. 2002 Nov 15;62(22):6651-8.