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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01117 | Chronic recurrent multifocal osteomyelitis | ... consisting of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and neutrophilic dermatosis. It has been reported that mutations in LPIN2 are responsible for this syndrome. | Immune system disease |
(CRMO1) LPIN2 [HSA:9663] [KO:K15728] (CRMO2) IL1RN [HSA:3557] [KO:K05481] (CRMO3) IL1R1 [HSA:3554] [KO:K04386] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |