ORPHA:573253
Split cord malformation type II
Synonyms: Diplomyelia · SCM type 2 · SCM type II · Split cord malformation type 2
- Type
- Morphological anomaly
- Group
- Disorder
- Age of onset
- Adolescent, Adult, Childhood, Infancy
- Status
- active
A rare subtype of split cord malformation characterized by both hemicords included in the same single dural sac. An intradural intervening mesenchymal septum may be present.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Split cord malformation type II | Diplomyelia · SCM type 2 · SCM type II · Split cord malformation type 2 |
| fr | Moelle épinière dédoublée type II | Diplomyélie · Moelle épinière dédoublée de type 2 · SCM type 2 · SCM type II |
| de | Split-Cord-Malformation Typ II | SCM Typ 2 · SCM Typ II · Split-Cord-Malformation Typ 2 |
| es | Malformación de médula espinal hendida tipo II | Malformación de médula espinal hendida tipo 2 |
| it | Malformazione da fissurazione longitudinale del midollo spinale tipo II | Malformazione da fissurazione longitudinale del midollo spinale tipo 2 · SCM tipo 2 · SCM tipo II |
| nl | Gespleten ruggenmerg-malformatie type II | Gespleten ruggenmerg-malformatie type 2 · SCM type 2 · SCM type II |
| pt | Malformação do cordão dividido tipo II | |
| pl | Malformacja rozszczepionego sznura typu II | = en |
| cs | Diastematomyelie, typ II | = en |
| uk | Розщеплення пуповини, тип II | Дипломієлія · SCM тип 2 · SCM тип II · Розщеплення пуповини, тип 2 |
| zh | 脊髓分裂畸形II型 | SCM type 2 · SCM type II · Split cord malformation type 2 |
| tr | Ayrık kordon malformasyonu tip II | SCM tip 2 · SCM tip II · Ayrık omurilik malformasyonu tip 2 |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q06.2 | NTBT | attributed | validated |
| ICD-11 | LA07.1 | NTBT | attributed | validated |
| MONDO | 0035541 | E | validated | |
| UMLS | C5680360 | 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:573278Split cord malformation
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
No children.
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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 | 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/573253
- This record as JSON: /data/d/573253.json