ORPHA:566857
Aprosencephaly
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
This disease is described under Aprosencephaly/atelencephaly spectrum
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Aprosencephaly | |
| fr | Aprosencéphalie | |
| de | Aprosenzephalie | |
| es | Aprosencefalia | |
| it | Aprosencefalia | |
| nl | Aprosencefalie | |
| pt | Aprosencefalia | |
| pl | Aprosencefalia | |
| cs | Aprosencefalie | |
| uk | Апросенцефалія | |
| zh | 脑前部缺无 | |
| tr | Aprosensefali |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q04.3 | NTBT | attributed | validated |
| ICD-11 | LA05.Y | NTBT | attributed | validated |
| MONDO | 0035450 | E | validated | |
| UMLS | C0431349 | 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:566847Aprosencephaly/atelencephaly spectrum
rare developmental anomalies during embryogenesis; 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/566857
- This record as JSON: /data/d/566857.json