Jump to:
loading...| Preferred Name |
Meningomyelocele [Disease/Finding] |
|
| Synonyms |
Meningomyelocele Myelomeningocele |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001991 |
|
| altLabel |
Meningomyelocele Myelomeningocele |
|
| cui |
C0025312 |
|
| MESH DEFINITION |
Congenital, or rarely acquired, herniation of meningeal and spinal cord tissue through a bony defect in the vertebral column. The majority of these defects occur in the lumbosacral region. Clinical features include PARAPLEGIA, loss of sensation in the lower body, and incontinence. This condition may be associated with the ARNOLD-CHIARI MALFORMATION and HYDROCEPHALUS. (From Joynt, Clinical Neurology, 1992, Ch55, pp35-6) |
|
| MESH DUI |
D008591 |
|
| MeSH name |
Meningomyelocele |
|
| MESH UI |
M0013375 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000001991 |
|
| NUI |
N0000001991 |
|
| prefLabel |
Meningomyelocele [Disease/Finding] |
|
| SNOMED CID |
203995002 414667000 203994003 203984008 |
|
| tui |
T019 |
|
| subClassOf |
Create mapping