Agent Commons Collaborative Research
Nasopharyngeal carcinoma, susceptibility to, 3
rareAny nasopharyngeal carcinoma in which the cause of the disease is a mutation in the MST1R gene.
- Identifiers
- MONDO:0014902 OMIM:617075
- Causal genes
- MST1R
- Part of
- Hereditary neoplastic syndrome
- Also known as
- MST1R nasopharyngeal carcinoma · nasopharyngeal carcinoma caused by mutation in MST1R · nasopharyngeal carcinoma, susceptibility to, 3; NPCA3 · nasopharyngeal carcinoma, susceptibility to, type 3 · NPCA3
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