ORPHA:182067
Glial tumor
Synonyms: Glioma
- Type
- Clinical group
- 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 | Glial tumor | Glioma |
| fr | Tumeur gliale | Gliome |
| de | Gliom | |
| es | Tumor glial | = en |
| it | Tumore gliale | = en |
| nl | Gliale tumor | Glioom |
| pt | Glioma | |
| pl | Guz glejowy | Glejak |
| cs | Gliální nádory | Gliomy |
| uk | Гліальна пухлина | Гліома |
| zh | 胶质瘤 | 神经胶质瘤 |
| tr | Glial tümör | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 137800 | E | validated | |
| OMIM | 607248 | BTNT | validated | |
| OMIM | 613028 | BTNT | validated | |
| OMIM | 613029 | BTNT | validated | |
| OMIM | 613030 | BTNT | validated | |
| OMIM | 613031 | BTNT | validated | |
| OMIM | 613032 | BTNT | validated | |
| OMIM | 613033 | BTNT | validated | |
| MONDO | 0021042 | E | validated | |
| MeSH | D005910 | E | validated | |
| UMLS | C0017638 | E | validated | |
| GARD | 6513 | E | validated | |
| MedDRA | 10018338 | 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 (1):
- ORPHA:251558Rare tumor of neuroepithelial tissue
rare neurological diseases; rare neoplastic diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
5 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 5.26 / 100 000 | United States | Value and class | Validated | Central Brain Tumor OTHERistry of the United States 2004[OTHER]_24193082[PMID] |
| Point prevalence | 1-5 / 10 000 | 26 / 100 000 | Europe | Value and class | Validated | European Medicines Agency 2018[OTHER] |
| Annual incidence | 1-9 / 100 000 | 5.7 / 100 000 | Greece | Value and class | Validated | 19494549[PMID] |
| Annual incidence | 1-9 / 100 000 | 6.2 / 100 000 | Croatia | Value and class | Validated | 15103760[PMID] |
| Annual incidence | 1-9 / 100 000 | 5.35 / 100 000 | Europe | Value and class | Validated | RARECARE surveillance of rare cancers in Europe[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/182067
- This record as JSON: /data/d/182067.json