ORPHA:100001
Sclerosing perineurioma
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sclerosing perineurioma | |
| fr | Périneuriome sclérosant | |
| de | Perineuriom, sklerosierendes | |
| es | Perineurioma esclerótico | |
| it | Perineurinoma sclerosante | |
| nl | Scleroserend perineurioom | |
| pt | Perineurioma esclerosante | |
| pl | Guz okołonerwowy/Onerwiak szkliwiejący | |
| cs | Sklerozující perineuriom | |
| uk | Склерозуюча периневріома | |
| zh | 硬化性神经鞘瘤 | |
| tr | Sklerozan perinörom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D36.1 | BTNT | attributed | validated |
| ICD-11 | 2F3Y | NTBT | index | validated |
| MONDO | 0015030 | E | validated | |
| UMLS | C5681811 | 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:100002Extraneural perineurioma
rare neurological diseases; rare neoplastic diseases
No children.
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/100001
- This record as JSON: /data/d/100001.json