autosomal dominant disease RASopathy Noonan syndrome with multiple lentigines GARD:1100 DOID:14291 Generalized lentiginosis OMIM:PS151100 NCI:C84820 ORDO:500 OMIM mapping confirmed by DO. [SN]. Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome SNOMEDCT_US_2020_03_01:111306001 MESH:D044542 UMLS_CUI:C0175704 disease_ontology LEOPARD syndrome A RASopathy that is characterized by autosomal dominant inheritance of brown skin spots called lentigines that are similar to freckles, heart defects, widely spaced eyes a sunken chest or protruding chest and short stature. Gorlin syndrome II Lentiginosis profusa syndrome Moynahan syndrome Multiple lentigines syndrome Progressive cardiomyopathic lentiginosis