ORPHA:252190
Inherited nervous system cancer-predisposing syndrome
- 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 | Inherited nervous system cancer-predisposing syndrome | |
| fr | Syndrome familial avec prédisposition aux cancers du système nerveux | |
| de | Krebsprädispositionssyndrom des Hirns, vererbtes | |
| es | Síndrome de predisposición hereditaria al cancer del sistema nervioso | |
| it | Sindrome ereditaria da predisposizione ai tumori del sistema nervoso | |
| nl | Overgeërfde zenuwstelselkanker-predisposerend syndroom | |
| pt | Síndrome de predisposição a cancro hereditário do sistema nervoso | |
| pl | Wrodzony zespół predysponujący do nowotworów układu nerwowego | |
| cs | Syndrom dědičné predispozice k rakovině nervového systému | |
| uk | Спадковий синдром схильності до раку нервової системи | |
| zh | 遗传性神经系统癌症易感综合征 | |
| tr | Kalıtsal sinir sistemi kanserine yatkınlık sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16756 | E | validated | |
| UMLS | C5680719 | 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:98006Rare neurologic disease
rare neurological diseases
Children (12):
- ORPHA:100Ataxia-telangiectasia
- ORPHA:251347Ataxia-telangiectasia-like disorder
- ORPHA:252202Constitutional mismatch repair deficiency syndrome
- ORPHA:377Gorlin syndrome
- ORPHA:443101Hypothalamic adipsic hypernatraemia syndrome
- ORPHA:524Li-Fraumeni syndrome
- ORPHA:252206Melanoma and neural system tumor syndrome
- ORPHA:2481Neurocutaneous melanocytosis
- ORPHA:634518Neurofibromatosis/schwannomatosis
- ORPHA:783Rubinstein-Taybi syndrome
- ORPHA:805Tuberous sclerosis complex
- ORPHA:892Von Hippel-Lindau disease
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/252190
- This record as JSON: /data/d/252190.json