ORPHA:645276
Spinal cord lipoma
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
A rare group of malformation characterized by the presence of lipomatous mass in direct contact with the spinal cord. It includes dysraphic (extramedullary) spinal cord lipomas and non-dysraphic (intramedullary) spinal cord lipoma.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spinal cord lipoma | |
| fr | Lipome médullaire | Lipome de la moelle épinière |
| de | Spinales Lipom | Spinale Lipomatose |
| es | Lipoma espinal | |
| it | Lipoma spinale | |
| nl | Lipoom van ruggenmerg | |
| pt | Lipoma espinhal | |
| pl | Tłuszczak rdzenia kręgowego | |
| cs | Lipom míchy | |
| uk | Ліпома спинного мозку |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0001790 | E | validated | |
| MONDO | 1790 | E | validated | |
| UMLS | C0347446 | E | validated | |
| MedDRA | 10064898 | 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:268357Neural tube closure defect
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
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/645276
- This record as JSON: /data/d/645276.json