ORPHA:98062
Rare nervous system tumor
Synonyms: Rare nervous system neoplasm
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare nervous system tumor | Rare nervous system neoplasm |
| fr | Tumeur rare du système nerveux | Néoplasie rare du système nerveux |
| de | Seltener Tumor des Nervensystems | |
| es | Tumor raro del sistema nervioso | |
| it | Tumore raro del sistema nervoso | |
| nl | Zeldzame tumor van zenuwstelsel | Zeldzaam neoplasma van zenuwstelsel |
| pt | Tumor do sistema nervoso, raro | |
| pl | Rzadki guz układu nerwowego | Rzadki nowotwór układu nerwowego |
| cs | Vzácné nádory nervového systému | Vzácné neoplázie nervového systému |
| uk | Рідкісна пухлина нервової системи | Рідкісне новоутворення нервової системи |
| zh | 罕见神经系统肿瘤 | 罕见神经系统肿瘤 |
| tr | Nadir sinir sistemi tümörü | Nadir sinir sistemi neoplazmı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680219 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:98006Rare neurologic disease
rare neurological diseases - ORPHA:98057Rare tumor
rare neoplastic diseases
Children (8):
- ORPHA:54595Craniopharyngioma
- ORPHA:252054Hemangioblastoma
- ORPHA:46135Primary central nervous system lymphoma
- ORPHA:251995Primary germ cell tumor of central nervous system
- ORPHA:279897Primary oculocerebral lymphoma
- ORPHA:251558Rare tumor of neuroepithelial tissue
- ORPHA:252057Tumor of cranial and spinal nerves
- ORPHA:252025Tumor of meninges
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/98062
- This record as JSON: /data/d/98062.json