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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]
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