Closed spinal dysraphism
Synonyms: Closed spina bifida · Occult spina bifida · Spina bifida occulta
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
A rare group of spinal dysraphisms, also referred to as spina bifida occulta, with a high variability in terms of severity,characterized by the absence of exposed neural tissue. The skin overlying the abnormality remains intact although the skin itself may be abnormal with features such as hairy patch of skin, crater or haemangioma. These skin features are known as the cutaneous stigmata of spinal dysraphism.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Closed spinal dysraphism | Closed spina bifida · Occult spina bifida · Spina bifida occulta |
| fr | Dysraphisme spinal fermé | Spina bifida caché · Spina bifida fermé · Spina bifida occulta |
| de | Spinale Dysraphie, geschlossene | Geschlossene Spina bifida · Spina bifida occulta · Verdeckte Spina bifida |
| es | Disrafismo espinal cerrado | Espina bífida cerrada · Espina bífida oculta |
| it | Disrafismo spinale chiuso | Spina bifida chiusa · Spina bifida occulta |
| nl | Gesloten spinale dysrafie | Gesloten spina bifida · Occulte open rug · Spina bifida occulta |
| pt | Disrafismo espinhal fechado | Espinha bífida fechada · Espinha bífida oculta |
| pl | Zamknięta wada dysraficzna kręgosłupa | = en |
| cs | Uzavřená spinální dysrafie | = en |
| uk | Закритий спінальний дизрафізм | Закрита spina bifida · Окультна spina bifida · Spina bifida occulta |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q76.0 | E | specific | validated |
| ICD-11 | LB73.0 | E | specific | validated |
| MONDO | 859 | E | validated | |
| MeSH | D016136 | E | validated | |
| UMLS | C0080174 | E | validated | |
| MedDRA | 10041525 | 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:823Spina bifida and other spinal dysraphisms
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
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/645202
- This record as JSON: /data/d/645202.json