DO_rare_slim NCIthesaurus has material basis in autosomal dominant disease RASopathy Noonan syndrome with multiple lentigines GARD:1100 DOID:14291 NCI:C84820 MIM:PS151100 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. ORDO:500 Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome Generalized lentiginosis Lentiginosis profusa syndrome SNOMEDCT_US_2025_09_01:111306001 MESH:D044542 Moynahan syndrome Multiple lentigines syndrome OMIM mapping confirmed by DO. [SN]. Progressive cardiomyopathic lentiginosis UMLS_CUI:C0175704 disease_ontology Gorlin syndrome II LEOPARD syndrome autosomal dominant inheritance