basal ganglia calcification
(Q1947307)
a rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement
a rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement
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Current Data About
basal ganglia calcification
| (P31) |
(Q42303753)
(Q929833) (Q112193867) |
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| (P138) |
(Q90083)
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| (P279) |
(Q4866181)
(Q108404609) |
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| (P373) |
Fahr's syndrome
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| (P1325) |
http://www.nanbyou.or.jp/entry/3838
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| (P1748) |
C129973
C179297 |
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| (P1995) |
(Q83042)
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| (P2293) |
(Q18031578)
(Q18030421)
(Q18030425)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0060230
http://identifiers.org/doid/DOID:0060230
http://www.orpha.net/ORDO/Orphanet_1980 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
Fahr disease childhood-onset idiopathic basal ganglia calcification idiopathic basal ganglia calcification Basal Ganglia Calcification, Idiopathic, 3 IBGC1 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1 Striopallidodentate Calcinosis, Bilateral Striopallidodentate Calcinosis, Autosomal Dominant, Adult-Onset Cerebral Calcification, Nonarteriosclerotic, Idiopathic, Adult-Onset Fahr Disease, Familial Ferrocalcinosis, Cerebrovascular Fahr Disease, Familial, Formerly Basal Ganglia Calcification, Idiopathic, 3, Formerly Fahr's disease Chavany-Brunhes syndrome Fritsche's syndrome Familial idiopathic basal ganglia calcification Idiopathic basal ganglia calcification disease |
| description | a rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement |
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