Disease: Leopard Syndrome 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551484
Disease: Leopard Syndrome 1
Leopard Syndrome 1 		0.300 Biomarker disease GENOMICS_ENGLAND A novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines. 25423878 2015