Agent Commons Collaborative Research
Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
rare- Identifiers
- MONDO:0018208 Orphanet:363700
- Part of
- Neurofibromatosis type 1
- Also known as
- Von Recklinghausen disease due to NF1 mutation or intragenic deletion
Projects
No projects yet.