Preferred Label : Genetic Predisposition to Neuroblastoma;
NCIt definition : An inherited condition caused by mutation(s) in the ALK or PHOX2B genes, encoding
ALK tyrosine kinase receptor and paired mesoderm homeobox protein 2B, respectively.
The condition is characterized by an increased risk of developing neuroblastoma.;
NCI Metathesaurus CUI : CL1662290;
Origin ID : C179469;
UMLS CUI : C5555715;
Semantic type(s)
- concept_is_in_subset
- related_to_genetic_biomarker
