Term info
                                    database cross reference
                                    
                                - Orphanet:471383 (MONDO:equivalentTo)
 
                                    
                                        Subsets
                                    
                                    
                                disease_grouping, ordo_group_of_disorders
                                        
                                            definition
                                        
                                        
                                An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.
                                        
                                            exactMatch
                                        
                                        
                                http://purl.obolibrary.org/obo/Orphanet_471383
                                        
                                            has exact synonym
                                        
                                        
                                hereditary lethal multiple congenital anomalies/dysmorphic syndrome
                                        
                                            id
                                        
                                        
                                MONDO:0043009


            