ORPHA:645273
Dysraphic spinal cord lipoma
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
A rare group of spinal cord lipoma characterized by the presence of extramedullary lipomatous mass located at any point along the spinal cord with or without a dural defect.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Dysraphic spinal cord lipoma | |
| fr | Lipome médullaire dysraphique | |
| de | Dysraphisches spinales Lipom | |
| es | Lipoma espinal disráfico | |
| it | Lipoma spinale disrafico | |
| nl | Lipoom van ruggenmerg met dysrafie | |
| pt | Lipoma espinhal disráfico | |
| pl | Dysraficzny tłuszczak rdzenia kręgowego | |
| cs | Dysrafický lipom míchy | |
| uk | Дизрафічна ліпома спинного мозку |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5816731 | 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:645202Closed spinal dysraphism
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases - ORPHA:645276Spinal cord lipoma
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:268832OBSOLETE: Lipoma associated with neurospinal dysraphism referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/645273
- This record as JSON: /data/d/645273.json