ORPHA:268950
Cerebral cortical dysplasia
Synonyms: Brain cortical dysplasia
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cerebral cortical dysplasia | Brain cortical dysplasia |
| fr | Dysplasie corticale cérébrale | |
| de | Dysplasie, kortikale zerebrale | Kortikale Dysplasie des Gehirns |
| es | Displasia cortical cerebral | Displasia cortical del cerebro |
| it | Displasia corticale cerebrale | Displasia corticale del cervello |
| nl | Cerebrale corticale dysplasie | Corticale dysplasie van de hersenen |
| pt | Displasia cortical cerebral | Displasia cortical do cérebro |
| pl | Dysplazja korowa mózgu | = en |
| cs | Cerebrální kortikální dysplázie | = en |
| uk | Дисплазія кори головного мозку | Дисплазія кори головного мозку |
| zh | 大脑皮质发育不良 | 大脑皮质发育不良 |
| tr | Serebral kortikal displazi | Beyin kortikal displazisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LA05.51 | E | specific | validated |
| MONDO | 0017094 | E | validated | |
| MONDO | 17094 | E | validated | |
| UMLS | C0431380 | 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:163209Non-syndromic cerebral malformation due to abnormal neuronal migration
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
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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.
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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/268950
- This record as JSON: /data/d/268950.json