Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:affectedArea |
gptkb:basal_ganglia
gptkb:cerebral_cortex gptkb:cerebellum |
| gptkbp:alsoKnownAs |
gptkb:Fahr's_disease
gptkb:Primary_Familial_Brain_Calcification |
| gptkbp:associatedWith |
gptkb:PDGFRB
gptkb:PDGFB gptkb:JAM2 gptkb:SLC20A2 gptkb:XPR1 MYORG |
| gptkbp:cause |
genetic disorder
|
| gptkbp:diagnosedBy |
gptkb:CT_scan
MRI |
| gptkbp:fullName |
gptkb:Adult-onset_Primary_Familial_Brain_Calcification
|
| https://www.w3.org/2000/01/rdf-schema#label |
APFBC
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:onset |
adulthood
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
movement disorders
cognitive impairment psychiatric symptoms |
| gptkbp:treatment |
symptomatic management
|
| gptkbp:bfsParent |
gptkb:Asian_Pacific_Federation_of_Biochemical_Societies
|
| gptkbp:bfsLayer |
6
|