idiopathic basal ganglia calcification
GPTKB entity
Statements (37)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
neurological disorder |
| gptkbp:affects |
gptkb:basal_ganglia
gptkb:cerebral_cortex gptkb:cerebellum |
| gptkbp:associatedWith |
gptkb:PDGFRB
gptkb:PDGFB gptkb:JAM2 gptkb:SLC20A2 gptkb:XPR1 MYORG |
| gptkbp:causedBy |
unknown
|
| gptkbp:diagnosedBy |
gptkb:CT_scan
MRI |
| gptkbp:frequency |
rare
|
| gptkbp:hasICD10 |
G23.8
|
| gptkbp:hasOrphanetID |
ORPHA:998
|
| https://www.w3.org/2000/01/rdf-schema#label |
idiopathic basal ganglia calcification
|
| gptkbp:inheritance |
autosomal dominant
sporadic |
| gptkbp:OMIM |
213600
|
| gptkbp:onset |
childhood
adulthood |
| gptkbp:symptom |
gptkb:dementia
seizures movement disorder parkinsonism psychiatric symptoms |
| gptkbp:synonym |
gptkb:Fahr's_disease
Fahr disease |
| gptkbp:treatment |
symptomatic treatment
|
| gptkbp:bfsParent |
gptkb:PDGFB
gptkb:PDGFR-beta gptkb:Pdgfrb gptkb:platelet-derived_growth_factor_receptor_beta gptkb:PDGF_receptor_beta |
| gptkbp:bfsLayer |
7
|