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LEOPARD syndrome 2

MONDO:0012691

Any Noonan syndrome with multiple lentigines in which the cause of the disease is a mutation in the RAF1 gene.

Also known as: LEOPARD syndrome 2, Leopard syndrome type 2, leopard syndrome 2, LPRD2

13 clinical trials for this condition and its sub-types, 0 tagged with LEOPARD syndrome 2 itself.

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