Pineal parenchymal tumor of intermediate differentiation
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare type of pineal parenchymal tumor (PPT) of intermediate-grade malignancy manifesting with visual disturbances, headaches, loss of coordination and balance, nausea and vomiting due to obstructive hydrocephalus, and that is classified as either grade II PPTID (pineal parenchymal tumor of intermediate differentiation) or grade III PPTID according to the degree of neuronal differentiation and mitotic activity.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pineal parenchymal tumor of intermediate differentiation | |
| fr | Tumeur du parenchyme pinéal à différenciation intermédiaire | |
| de | Parenchymatöser Pinealistumor intermediärer Differenzierung | |
| es | Tumor del parénquima pineal de diferenciación intermedia | |
| it | Tumore del parenchima pineale a differenziazione intermedia | |
| nl | Pineale parenchymale tumor van intermediaire differentiatie | |
| pt | Tumor do parênquima pineal de diferenciação intermédia | |
| pl | Guz miąższu szyszynki o pośrednim zróżnicowaniu | |
| cs | Pineální parenchymatózní nádor středního stupně diferenciace | |
| uk | Паренхіматозна пухлина шишкоподібної залози проміжного диференціювання | |
| zh | 松果体中分化实质瘤 | |
| tr | Ara farklılaşmanın epifiz parankimal tümörü |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D44.5 | NTBT | attributed | validated |
| ICD-11 | 2A00.20 | NTBT | index | validated |
| ICD-11 | XH1S48 | NTBT | index | validated |
| MONDO | 0006369 | E | validated | |
| UMLS | C1367859 | E | validated | |
| GARD | 10644 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:251905Pineal tumor of neuroepithelial tissue
rare neurological diseases; rare neoplastic diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/251919
- This record as JSON: /data/d/251919.json