ORPHA:102011
Lissencephaly type 3
- 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 | Lissencephaly type 3 | |
| fr | Lissencéphalie de type 3 | |
| de | Lissenzephalie Typ 3 | |
| es | Lisencefalia tipo 3 | |
| it | Lissencefalia, tipo 3 | |
| nl | Lissencefalie type 3 | |
| pt | Lisencefalia tipo 3 | |
| pl | Lizencefalia typu 3 | |
| cs | Lisencefalie, typ 3 | |
| uk | Лісенцефалія, тип 3 | |
| zh | 无脑回畸形3型 | |
| tr | Lizensefali tip 3 |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD20.1 | NTBT | index | validated |
| MONDO | 0015148 | E | validated | |
| MONDO | 15148 | E | validated | |
| MeSH | C566908 | E | validated | |
| UMLS | C1969029 | 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:48471Lissencephaly
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
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/102011
- This record as JSON: /data/d/102011.json