has material basis in germline mutation in LPIN2 chronic recurrent multifocal osteomyelitis Majeed syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/6746 https://github.com/monarch-initiative/mondo/issues/6747 https://github.com/monarch-initiative/mondo/issues/6751 https://rarediseases.info.nih.gov/diseases/10088/majeed-syndrome https://www.malacards.org/card/majeed_syndrome Orphanet:77297 Majeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis. Majeed syndrome CDA and CRMO UMLS:C1864997 MEDGEN:351273 SCTID:703540008 MESH:C537839 MONDO:0012316 congenital dyserythropoietic anaemia and chronic recurrent multifocal osteomyelitis chronic recurrent multifocal osteomyelitis, congenital chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis NANDO:2200453 icd11.foundation:1316564349 OMIM:609628 MJDS GARD:0010088 NCIT:C119058 dyserythropoietic anemia, and neutrophilic dermatosis MedDRA:10072223 ICD9:759.89 DOID:0061224