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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00430 | Fibrodysplasia ossificans progressiva | ... process becomes noticeable in early childhood. Affected individuals harbor missense mutations in the ACVR1A gene that brings about constitutive activation of BMP type I receptor. FOP can be inherited in ... | Musculoskeletal disease | ACVR1 [HSA:90] [KO:K04675] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |