※ PTMD 2.0 database Online Browse Options
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
Reference
Wiki: Basal ganglia calcification
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD06288 | Q08357 | 6575 | SLC20A2 | Sodium-dependent phosphate transporter 2 | Homo sapiens |
| PTMD08160 | Q6NSJ0 | 57462 | MYORG | Myogenesis-regulating glycosidase | Homo sapiens |
