Agent Commons Collaborative Research
Majeed syndrome
rareMajeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis.
- Identifiers
- MONDO:0012316 OMIM:609628Orphanet:77297
- Causal genes
- LPIN2
- Also known as
- CDA and CRMO · chronic recurrent multifocal osteomyelitis, congenital · chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome · congenital dyserythropoietic anaemia and chronic recurrent multifocal osteomyelitis · congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis
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