Split cord malformation
Synonyms: SCM
- Type
- Clinical group
- Group
- Group of disorders
- Age of onset
- Adolescent, Adult, Childhood, Infancy
- Status
- active
A rare malformation characterized by localized longitudinal division of the spinal cord into two "hemicords". Vertebro-costal anomalies are commonly associated. Classic overlying skin stigmata is a focal hypertrichosis/hairy patch. Split cord malformations may be associated with other dysraphic anomalies (eg: filum lipoma).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Split cord malformation | SCM |
| fr | Moelle épinière dédoublée | = en |
| de | Split-Cord-Malformation | = en |
| es | Malformación de médula espinal hendida | |
| it | Malformazione da fissurazione longitudinale del midollo spinale | = en |
| nl | Gespleten ruggenmerg-malformatie | = en |
| pt | Malformação do cordão dividido | |
| pl | Malformacja rozszczepionego sznura | = en |
| cs | Diastematomyelie | = en |
| uk | Розщеплення пуповини | = en |
| zh | 脊髓分裂畸形 | = en |
| tr | Bölünmüş kord malformasyonu | = en |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q06.2 | NTBT | attributed | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:645202Closed spinal dysraphism
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases - ORPHA:268843Malformation of the neurenteric canal, spinal cord and column
rare developmental anomalies during embryogenesis; rare neurological diseases
Genes
0 directOrphanet records no gene directly on this code.
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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/573278
- This record as JSON: /data/d/573278.json