You are using an outdated browser. Please upgrade your browser to improve your experience.
LEOPARD syndrome 3
Disease Summary
Associated Targets (1)
Tclin
1
Mondo Description Any Noonan syndrome with multiple lentigines in which the cause of the disease is a mutation in the BRAF gene.
Uniprot Description A disorder characterized by lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormalities of genitalia, retardation of growth, and sensorineural deafness.