Hemi-myelomeningocele
Synonyms: Open split-cord malformation
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Unknown
- Status
- active
A very rare form of composite dysraphism characterized by the presence of a split cord malformation and a myelomeningocele on one of the two hemicords. Hemicords can be in a single dural sac or in two separated dural sacs. Other spinal cord malformations can be associated. Due to the comparable prognosis it is considered as a subtype of myelomeningocele.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hemi-myelomeningocele | Open split-cord malformation |
| fr | Hémi-myélomeningocèle | Moelle épinière dédoublée ouverte |
| de | Hemimyelomeningozele | Split-Cord-Malformation, offene |
| es | Hemimielomeningocele | Malformación abierta del cordón espinal hendido |
| it | Emi-mielomeningocele | Malformazione aperta da fissurazione della corda spinale |
| nl | Hemi-myelomeningocele | Hemimyelomeningocele · Open 'split cord'-malformatie |
| pt | Hemi-mielomeningocelo | Malformação de espinha bífida aberta |
| pl | Przepuklina oponowo-rdzeniowa z podziałem rdzenia | = en |
| cs | Hemi-myelomeningokéla | = en |
| uk | Гемі-мієломенінгоцеле | Відкрита вада розвитку розщеплення пуповини |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0957454 | E | validated | |
| UMLS | C5816710 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:93969Open spinal dysraphism with a myelomeningocele
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/645388
- This record as JSON: /data/d/645388.json