ORPHA:268994
Isolated focal cortical dysplasia type II
Synonyms: Cortical dysplasia, Taylor type · FCD type II · Isolated focal cortical dysplasia type 2
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated focal cortical dysplasia type II | Cortical dysplasia, Taylor type · FCD type II · Isolated focal cortical dysplasia type 2 |
| fr | Dysplasie corticale focale isolée type II | Dysplasie corticale de Taylor · Dysplasie corticale focale isolée type 2 · FCD type II |
| de | Kortikale Dysplasie, fokale isolierte, Typ II | FCD Typ II · Kortikale Dysplasie Typ Taylor |
| es | Displasia cortical focal aislada tipo II | Displasia cortical focal aislada tipo 2 · Displasia cortical tipo Taylor · FCD tipo II |
| it | Displasia corticale focale isolata, tipo II | Displasia corticale focale isolata, tipo 2 · Displasia corticale, tipo Taylor · FCD, tipo II |
| nl | Geïsoleerde focale corticale dysplasie type II | Corticale dysplasie, Taylor-type · FCD type II · Geïsoleerde focale corticale dysplasie type 2 |
| pt | Displasia cortical focal isolada tipo II | FCD tipo II |
| pl | Izolowana dysplazja korowa mózgu typu II | FCD typu II |
| cs | Izolovaná fokální kortikální dysplázie, typ II | Kortikální dysplázie, typ II · FCD type II · Izolovaná fokální kortikální dysplázie, typ 2 |
| uk | Ізольована фокальна кортикальна дисплазія, тип II | Кортикальна дисплазія, тип Тейлора · FCD тип II · Ізольована вогнищева кортикальна дисплазія типу 2 |
| zh | 孤立性局灶性脑皮质发育不良II型 | 孤立性局灶性皮质发育不良2型 |
| tr | İzole fokal kortikal displazi tip II | FCD tip II · Kortikal displazi, Taylor tip · İzole fokal kortikal displazi tip 2 |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 607341 | E | validated | |
| ICD-10 | Q04.8 | NTBT | attributed | validated |
| ICD-11 | LA05.51 | NTBT | index | validated |
| MONDO | 0011818 | E | validated | |
| UMLS | C5679769 | E | validated | |
| GARD | 10190 | 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:65683Isolated focal cortical dysplasia
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/268994
- This record as JSON: /data/d/268994.json