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Browse result for Basal ganglia calcification

※ introduction

    Primary familial brain calcification (PFBC), also known as familial idiopathic basal ganglia calcification (FIBGC) and Fahr's disease, is a rare, genetically dominant or recessive, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement. Through the use of CT scans, calcifications are seen primarily in the basal ganglia and in other areas such as the cerebral cortex.

Reference
Wiki: Basal ganglia calcification



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD06288Q083576575
SLC20A2
Sodium-dependent phosphate transporter 2
Homo sapiens
PTMD08160Q6NSJ057462
MYORG
Myogenesis-regulating glycosidase
Homo sapiens