ORPHA:199633
Non-syndromic cerebral malformation
Synonyms: Non-syndromic brain malformation
- Type
- Category
- 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 | Non-syndromic cerebral malformation | Non-syndromic brain malformation |
| fr | Malformation cérébrale non syndromique | |
| de | Zerebrale Fehlbildung, nicht syndromale | Hirnfehlbildung, nicht syndromale |
| es | Malformación cerebral no sindrómica | Malformación del cerebro no sindrómica |
| it | Malformazione cerebrale | Malformazione del cervello |
| nl | Niet-syndromale cerebrale malformatie | Niet-syndromale malformatie van hersenen |
| pt | Malformação cerebral não-sindromática | Malformação do cérebro não-sindromática |
| pl | Malformacja mózgu | Wada mózgu |
| cs | Cerebrální malformace | Malformace mozku |
| uk | Несиндромальна церебральна мальформація | Несиндромальна вада розвитку головного мозку |
| zh | 非综合征性脑畸形 | 非综合征性脑畸形 |
| tr | Non-sendromik serebral malformasyon | Sendromik olmayan beyin malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16054 | E | validated | |
| UMLS | C0266449 | 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:729560Forebrain malformation
rare developmental anomalies during embryogenesis; rare neurological diseases
Children (10):
- ORPHA:319192Diencephalic-mesencephalic junction dysplasia
- ORPHA:269190Encephaloclastic disorder
- ORPHA:99802Hemimegalencephaly
- ORPHA:268936Isolated arhinencephaly
- ORPHA:199642Isolated congenital microcephaly
- ORPHA:200Isolated corpus callosum agenesis
- ORPHA:2477Isolated megalencephaly
- ORPHA:268926Midline cerebral malformation
- ORPHA:163209Non-syndromic cerebral malformation due to abnormal neuronal migration
- ORPHA:1665Sporadic fetal brain disruption sequence
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/199633
- This record as JSON: /data/d/199633.json