Chronic recurrent multifocal osteomyelitis with congenital dyserythropoietic anemia

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Subtype of: Recurrent multifocal osteomyelitis
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Chronic recurrent multifocal osteomyelitis with congenital dyserythropoietic anemia
MONDO_0012316
LPIN2 Unknown
29912021
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Chronic recurrent multifocal osteomyelitis with congenital dyserythropoietic anemia.
5 View disease cluster →
Majeed syndrome 1 shared geneLPIN2 Related via 1 shared gene including LPIN2. Multifocal osteomyelitis 1 shared geneLPIN2 Related via 1 shared gene including LPIN2. Microcytic anemia 1 shared geneLPIN2 Related via 1 shared gene including LPIN2. Congenital dyserythropoietic anemia 1 shared geneLPIN2 Related via 1 shared gene including LPIN2. Bullous pemphigoid 1 shared geneLPIN2 Related via 1 shared gene including LPIN2.