Statements (33)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
rare neurological disorder
|
| gptkbp:affects |
gptkb:basal_ganglia
gptkb:cerebral_cortex gptkb:cerebellum |
| gptkbp:alsoKnownAs |
gptkb:Primary_Familial_Brain_Calcification
|
| gptkbp:associatedWith |
gptkb:PDGFRB
gptkb:PDGFB gptkb:SLC20A2 gptkb:XPR1 MYORG |
| gptkbp:category |
genetic disorder
neurological disorder movement disorder |
| gptkbp:cause |
genetic mutations
|
| gptkbp:characterizedBy |
abnormal calcium deposits in the brain
|
| gptkbp:diagnosedBy |
gptkb:CT_scan
MRI |
| gptkbp:firstDescribed |
1930
Karl Theodor Fahr |
| gptkbp:hasNo |
cure
|
| https://www.w3.org/2000/01/rdf-schema#label |
Fahr's disease
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:prevalence |
very rare
|
| gptkbp:symptom |
gptkb:dementia
movement disorders seizures gait disturbance parkinsonism psychiatric symptoms speech impairment |
| gptkbp:treatment |
symptomatic management
|
| gptkbp:bfsParent |
gptkb:APFBC
|
| gptkbp:bfsLayer |
7
|