loading...| Preferred Name |
Spina Bifida Occulta [Disease/Finding] |
|
| Synonyms |
Spina Bifida Occulta Occult Spina Bifida Spinal Bifida, Closed |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003374 |
|
| altLabel |
Spina Bifida Occulta Occult Spina Bifida Spinal Bifida, Closed |
|
| cui |
C0080174 |
|
| MESH DEFINITION |
A common congenital midline defect of fusion of the vertebral arch without protrusion of the spinal cord or meninges. The lesion is also covered by skin. L5 and S1 are the most common vertebrae involved. The condition may be associated with an overlying area of hyperpigmented skin, a dermal sinus, or an abnormal patch of hair. The majority of individuals with this malformation are asymptomatic although there is an increased incidence of tethered cord syndrome and lumbar SPONDYLOSIS. (From Joynt, Clinical Neurology, 1992, Ch55, p34) |
|
| MESH DUI |
D016136 |
|
| MeSH name |
Spina Bifida Occulta |
|
| MESH UI |
M0024645 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000003374 |
|
| NUI |
N0000003374 |
|
| prefLabel |
Spina Bifida Occulta [Disease/Finding] |
|
| SNOMED CID |
76916001 |
|
| tui |
T019 |
|
| subClassOf |