ORPHA:165652
Rare genetic gastroenterological disease
- 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 | Rare genetic gastroenterological disease | |
| fr | Maladie gastroentérologique génétique rare | |
| de | Gastroenterologische Krankheit, genetisch bedingte | |
| es | Enfermedades gastroenterológicas genéticas raras | |
| it | Malattia gastroenterologica di origine genetica | |
| nl | Zeldzame genetische gastro-enterologische ziekte | |
| pt | Doença genética gastroenterológica | |
| pl | Rzadka genetyczna choroba gastroenterologiczna | |
| cs | Vzácná geneticky podmíněná gastroenterologická onemocnění | |
| uk | Рідкісне генетично обумовлене гастроентерологічне захворювання | |
| zh | 罕见遗传性胃肠疾病 | |
| tr | Nadir görülen genetik gastroenterolojik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15615 | E | validated | |
| UMLS | C5680439 | 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:98053Rare genetic disease
rare genetic diseases
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/165652
- This record as JSON: /data/d/165652.json