ORPHA:163209
Non-syndromic cerebral malformation due to abnormal neuronal migration
Synonyms: Brain malformation due to abnormal neuronal migration
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic cerebral malformation due to abnormal neuronal migration | Brain malformation due to abnormal neuronal migration |
| fr | Malformation cérébrale non syndromique due à une anomalie de la migration neuronale | |
| de | Zerebrale Fehlbildung durch neuronalen Migrationsdefekt, nichtsyndromal | Hirnfehlbildung durch Anomalie der neuronalen Migration |
| es | Malformación cerebral no sindrómica por migración neuronal anómala | Malformación del cerebro por migración neuronal anómala |
| it | Malformazione cerebrale non sindromica da difetto della migrazione neuronale | Malformazione cerebrale da difetto della migrazione neuronale |
| nl | Niet-syndromale cerebrale malformatie door abnormale neuronale migratie | Hersenmalformatie door abnormale neuronale migratie |
| pt | Doença neurológica por migração neuronal anómala | |
| pl | Niesyndromiczna malformacja mózgu z powodu nieprawidłowej migracji neuronów | Malformacja mózgu z powodu nieprawidłowej migracji neuronów |
| cs | Nesyndromické malformace mozku způsobené abnormální neuronální migrací | Malformace mozku způsobené abnormální neuronální migrací |
| uk | Несиндромальна церебральна мальформація внаслідок аномальної міграції нейронів | Вади розвитку мозку через аномальну міграцію нейронів |
| zh | 神经元异常迁移所致非综合征性脑畸形 | 神经元异常迁移所致脑畸形 |
| tr | Anormal nöronal migrasyon nedeniyle sendromik olmayan serebral malformasyon | Anormal nöronal göçe bağlı beyin malformasyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15572 | E | validated | |
| UMLS | C5679571 | 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 (3):
- ORPHA:166478Cerebral malformation with epilepsy
rare genetic diseases; rare neurological diseases - ORPHA:269553Genetic cerebral malformation
rare genetic diseases - ORPHA:199633Non-syndromic cerebral malformation
rare developmental anomalies during embryogenesis; rare neurological diseases
Children (8):
- ORPHA:329329Autosomal recessive frontotemporal pachygyria
- ORPHA:268950Cerebral cortical dysplasia
- ORPHA:300570Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
- ORPHA:2149Nodular neuronal heterotopia
- ORPHA:280640Occipital pachygyria and polymicrogyria
- ORPHA:2798Pachygyria-intellectual disability-epilepsy syndrome
- ORPHA:35981Polymicrogyria
- ORPHA:99796Subcortical band heterotopia
Codes that Orphanet moved or referred to this one:
- ORPHA:1139OBSOLETE: Arthrogryposis-epileptic seizures-migrational brain disorder syndrome referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/163209
- This record as JSON: /data/d/163209.json