ORPHA:645340
Non-terminal myelocystocele
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Unknown
- Status
- active
A rare closed spinal dysraphism characterized by myelocystocele located above the conus region. Also considered as a form of saccular limited dorsal myeloschisis.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-terminal myelocystocele | |
| fr | Myélocystocèle non-terminale | |
| de | Myelozystozele, nicht-terminale | |
| es | Mielocistocele no terminal | |
| it | Mielocistocele non terminale | |
| nl | Niet-terminale myelocystocele | |
| pt | Mielocistocelo não-terminal | |
| pl | Rozszczep nieterminalnego odcinka kręgosłupa z przepukliną rdzenia | |
| cs | Neterminální myelocystokéla | |
| uk | Нетермінальне мієлоцистоцеле |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q05.9 | NTBT | attributed | validated |
| MONDO | 0957451 | E | validated | |
| UMLS | C5816719 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:268813Myelocystocele
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/645340
- This record as JSON: /data/d/645340.json