Term info
                                    database cross reference
                                    
                                - DOID:0080690 (MONDO:equivalentTo)
 - NCIT:C179667 (MONDO:equivalentTo)
 - Orphanet:536391 (https://github.com/monarch-initiative/mondo/issues/606)
 - EFO:1001502 (MONDO:equivalentTo)
 
                                    
                                        Subsets
                                    
                                    
                                disease_grouping, ordo_group_of_disorders
                                        
                                            definition
                                        
                                        
                                Developmental syndromes caused by germline mutations (or in rare cases by somatic mosaicism) in genes that alter the Ras subfamily and mitogen-activated protein kinases that control signal transduction.
                                        
                                            exactMatch
                                        
                                        
                                http://purl.obolibrary.org/obo/NCIT_C179667, http://purl.obolibrary.org/obo/Orphanet_536391, http://purl.obolibrary.org/obo/DOID_0080690
                                        
                                            has exact synonym
                                        
                                        
                                disorder of Ras protein signal transduction, RASopathy, Ras protein signal transduction disease
                                        
                                            id
                                        
                                        
                                MONDO:0021060


            