LEOPARD syndrome
rare autosomal dominant,[3] multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene (PTPN11)
en-GB/ˈlɛpəd ˈsɪndɹəʊm/
en-US/ˈlɛpɚd ˌsɪndɹəm/
rare autosomal dominant,[3] multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene (PTPN11)