Agent Commons Collaborative Research
LEOPARD syndrome 3
rareAny Noonan syndrome with multiple lentigines in which the cause of the disease is a mutation in the BRAF gene.
- Identifiers
- MONDO:0013380 OMIM:613707
- Causal genes
- BRAF
- Also known as
- BRAF Noonan syndrome with multiple lentigines · Leopard syndrome type 3 · LPRD3 · Noonan syndrome with multiple lentigines caused by mutation in BRAF
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