ORPHA:645288
Terminal extramedullary conus spinal cord lipoma
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Unknown
- Status
- active
A rare form of extramedullary conus region spinal cord lipoma characterized by its location, extending from the poorly delineated tip of the conus.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Terminal extramedullary conus spinal cord lipoma | |
| fr | Lipome spinal extramédullaire terminal du cône | |
| de | Terminales extramedulläres Lipom des Conus spinalis | |
| es | Lipoma extramedular del cono medular terminal | |
| it | Lipoma spinale extramidollare terminale del cono | |
| nl | Terminaal extramedullair lipoom van conus medullaris | |
| pt | Lipoma extramedular terminal do cone medular | |
| pl | Tłuszczak zewnątrzrdzeniowy końcowego odcinka stożka rdzenia kręgowego | |
| cs | Terminální extramedulární lipom konusu míšního | |
| uk | Термінальна екстрамедулярна конусоподібна ліпома спинного мозку |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0970957 | E | validated | |
| UMLS | C5816727 | 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:645297Extramedullary conus spinal cord lipoma
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
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/645288
- This record as JSON: /data/d/645288.json