LEOPARD syndrome 3

MONDO:0013380

Any Noonan syndrome with multiple lentigines in which the cause of the disease is a mutation in the BRAF gene.

Also known as: BRAF Noonan syndrome with multiple lentigines, LEOPARD syndrome 3, Leopard syndrome type 3, Noonan syndrome with multiple lentigines caused by mutation in BRAF, leopard syndrome 3, LPRD3

13 clinical trials for this condition and its sub-types, 0 tagged with LEOPARD syndrome 3 itself.

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Part of

↑ Noonan syndrome with multiple lentigines (3)

Including sub-types (13) Tagged with LEOPARD syndrome 3 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.