ORPHA:268817
Cephalocele
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cephalocele | |
| fr | Céphalocèle | |
| de | Zephalozele | |
| es | Cefalocele | |
| it | Cefalocele | |
| nl | Cefalocele | |
| pt | Cefalocelo | |
| pl | Przepuklina mózgowa | |
| cs | Cefalokéla | |
| uk | Цефалоцеле | |
| zh | 脑膨出 | |
| tr | Sefalosel |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q01 | E | specific | validated |
| ICD-11 | LA01 | E | specific | validated |
| MONDO | 0017078 | E | validated | |
| MONDO | 17078 | E | validated | |
| UMLS | C0014065 | 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:268843Malformation of the neurenteric canal, spinal cord and column
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/268817
- This record as JSON: /data/d/268817.json