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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01574 |
Familial idiopathic basal ganglia calcification Bilateral striopallidodentate calcinosis (BSPDC) Fahr disease |
Familial idiopathic basal ganglia calcification (IBGC), also known as Fahr disease, is an inherited neurological disorder characterized by symmetrical calcification of cerebral structures lacking known ... | Nervous system disease |
(IBGC1) SLC20A2 [HSA:6575] [KO:K14640] (IBGC4) PDGFRB [HSA:5159] [KO:K05089] (IBGC5) PDGFB [HSA:5155] [KO:K17386] (IBGC6) XPR1 [HSA:9213] [KO:K24195] (IBGC7) MYORG [HSA:57462] [KO:K24727] (IBGC8) JAM2 [HSA:58494] [KO:K06735] (IBGC9) NAA60 [HSA:79903] [KO:K21121] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |