ORPHA:566852
Atelencephaly
Synonyms: Atelencephalic microcephaly
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
This disease is described under Aprosencephaly/atelencephaly spectrum
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Atelencephaly | Atelencephalic microcephaly |
| fr | Atélencéphalie | Microcéphalie atélencéphalique |
| de | Atelenzephalie | Mikrocephalyie, atelencephale |
| es | Atelencefalia | Microcefalia atelencefálica |
| it | Atelencefalia | Microcefalia atelencefalica |
| nl | Atelencefalie | Atelencefalische microcefalie |
| pt | Atelencefalia | |
| pl | Atelencefalia | = en |
| cs | Atelencefalie | = en |
| uk | Ателенцефалія | Ателенцефальна мікроцефалія |
| zh | 脑发育不全 | 脑发育不全性小头畸形 |
| tr | Atelensefali | Atelensefalik mikrosefali |
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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 | 0035449 | E | validated | |
| UMLS | C0431348 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:566847Aprosencephaly/atelencephaly spectrum
rare developmental anomalies during embryogenesis; rare neurological diseases
No children.
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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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/566852
- This record as JSON: /data/d/566852.json