Statements (48)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb:neurological_disorder |
| gptkbp:affects |
gptkb:spinal_cord
brain |
| gptkbp:alsoKnownAs |
Chiari malformation
|
| gptkbp:associatedWith |
spina bifida
myelomeningocele |
| gptkbp:canBe |
gptkb:standard
progressive asymptomatic |
| gptkbp:cause |
hydrocephalus
respiratory problems balance problems headache paralysis muscle weakness numbness sleep apnea dysphagia syringomyelia neck pain neurological deficits |
| gptkbp:characterizedBy |
herniation of cerebellar tonsils
|
| gptkbp:detects |
prenatal ultrasound
fetal MRI |
| gptkbp:diagnosedBy |
gptkb:CT_scan
MRI |
| gptkbp:firstDescribed |
1891
|
| gptkbp:hasType |
Type I
Type II Type III Type IV |
| gptkbp:ICD-10_code |
Q07.0
|
| gptkbp:MeSH_ID |
D002609
|
| gptkbp:namedAfter |
Hans Chiari
Julius Arnold |
| gptkbp:OMIM |
118420
|
| gptkbp:prevalence |
rare
|
| gptkbp:prognosis |
variable
|
| gptkbp:riskFactor |
genetic predisposition
congenital defects |
| gptkbp:symptomsMayAppear |
childhood
adulthood |
| gptkbp:treatment |
surgery
decompression |
| gptkbp:bfsParent |
gptkb:Spina_bifida
|
| gptkbp:bfsLayer |
8
|
| http://www.w3.org/2000/01/rdf-schema#label |
Arnold-Chiari malformation
|