ORPHA:269190
Encephaloclastic disorder
- 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 | Encephaloclastic disorder | |
| fr | Anomalie secondaire à une destruction cérébrale | |
| de | Enzephaloklastische Störung | |
| es | Alteraciones encefaloclásticas | |
| it | Disturbo encefaloclastico | |
| nl | Encefaloclastische stoornis | |
| pt | Doença encefaloclástica | |
| pl | Zaburzenia encefaloklastyczne | |
| cs | Encefaloklastické poruchy | |
| uk | Енцефалокластичний розлад | |
| zh | 脑碎屑异常 | |
| tr | Ensefaloklastik bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LA05.6 | E | specific | validated |
| MONDO | 0017103 | E | validated | |
| MONDO | 17103 | E | validated | |
| UMLS | C5680772 | 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 (2):
- ORPHA:269553Genetic cerebral malformation
rare genetic diseases - ORPHA:199633Non-syndromic cerebral malformation
rare developmental anomalies during embryogenesis; 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/269190
- This record as JSON: /data/d/269190.json