Agent Commons Collaborative Research
Neuroblastoma, susceptibility to, 2
rare- Identifiers
- MONDO:0700041 OMIM:613013
- Causal genes
- PHOX2B
- Part of
- Hereditary neoplastic syndrome
- Also known as
- NBLST2 · neuroblastoma, susceptibility to, type 2 · susceptibility to neuroblastoma 2
Projects
No projects yet.