ORPHA:48736
Embryonal carcinoma of the central nervous system
Synonyms: Embryonal carcinoma of the CNS
- 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 | Embryonal carcinoma of the central nervous system | Embryonal carcinoma of the CNS |
| fr | Carcinome embryonnaire du système nerveux central | Carcinome embryonnaire du SNC |
| de | Embryonalkarzinom des Zentralnervensystems | |
| es | Carcinoma embrionario del sistema nervioso central | Carcinoma embrionario del SNC |
| it | Carcinoma embrionale del sistema nervoso centrale | Carcinoma embrionale del SNC |
| nl | Embryonaal carcinoom van centraal zenuwstelsel | Embryonaal carcinoom van CZS |
| pt | Carcinoma embrionário intracraniano | |
| pl | Guz embrionalny centralnego układu nerwowego | Guz embrionalny CUN |
| cs | Embryonální karcinom centrálního nervového systému | Embryonální karcinom CNS |
| uk | Ембріональна карцинома центральної нервової системи | Ембріональна карцинома ЦНС |
| zh | 中枢神经系统胚胎性癌 | 中枢神经系统胚胎癌 |
| tr | Santral sinir sisteminin embriyonal karsinomu | MSS'nin embriyonal karsinomu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C71.9 | NTBT | attributed | validated |
| MONDO | 0018843 | E | validated | |
| UMLS | C1333377 | 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:180226Embryonal carcinoma
rare neoplastic diseases; rare transplant-related disorders - ORPHA:251995Primary germ cell tumor of central nervous system
rare neurological diseases; rare neoplastic diseases; rare transplant-related disorders
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/48736
- This record as JSON: /data/d/48736.json