ORPHA:314697
Acquired porencephaly
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Porencephaly
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired porencephaly | |
| fr | Porencéphalie acquise | |
| de | Porenzephalie, erworbene | |
| es | Porencefalia adquirida | |
| it | Porencefalia acquisita | |
| nl | Verworven porencefalie | |
| pt | Porencefalia adquirida | |
| pl | Porencefalia nabyta | |
| cs | Získaná porencefalie | |
| uk | Набута поренцефалія | |
| zh | 后天性脑穿通畸形 | |
| tr | Edinsel porensefali |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G93.0 | NTBT | inclusion | validated |
| ICD-11 | 8D68 | E | specific | validated |
| MONDO | 0017815 | E | validated | |
| UMLS | C0151860 | 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:2940Porencephaly
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/314697
- This record as JSON: /data/d/314697.json