ORPHA:268926
Midline cerebral malformation
Synonyms: Midline 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Midline cerebral malformation | Midline brain malformation |
| fr | Malformation cérébrale médiane | |
| de | Mittelliniendefekt des Gehirns | Zerebrale Fehlbildung im Bereich der Mittellinie |
| es | Malformación de la linea media cerebral | |
| it | Malformazione cerebrale della linea mediana | |
| nl | Middellijn cerebrale malformatie | Middellijn hersenmalformatie |
| pt | Malformação cerebral da linha média | Malformação do cérebro da linha média |
| pl | Malformacje linii pośrodkowej mózgu | = en |
| cs | Středočárové malformace mozku | Středočárová mozková malformace |
| uk | Серединна церебральна мальформація | Серединна вада розвитку головного мозку |
| zh | 脑中线畸形 | 脑中线畸形 |
| tr | Orta hat serebral malformasyon | Orta hat beyin malformasyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17090 | E | validated | |
| UMLS | C5679771 | 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 (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.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/268926
- This record as JSON: /data/d/268926.json