Term info
                                        
                                            IAO 0000233
                                        
                                        
                                https://github.com/monarch-initiative/mondo/issues/1270
                                        
                                            comment
                                        
                                        
                                This is a place-holder for Orphanet term ORDO_98849 which is not currently part of the rare genetic disorders imported from ORDO2 (as of January 2016).
                                        
                                            id
                                        
                                        
                                MONDO:0006440
                                        
                                            term replaced by
                                        
                                        
                                MONDO:0020332


 
            