ORPHA:101936
Rare gastroesophageal 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 gastroesophageal disease | |
| fr | Maladie gastro-oesophagienne rare | |
| de | Gastro-oesophageale Krankheit, seltene | |
| es | Enfermedad gastroesofágica rara | |
| it | Malattia gastroesofagea rara | |
| nl | Zeldzame gastro-oesofageale ziekte | |
| pt | Doença gastro-esofágica, rara | |
| pl | Rzadkie choroby żołądkowo-przełykowe | |
| cs | Vzácná gastroezofageální onemocnění | |
| uk | Рідкісне гастроезофагеальне захворювання | |
| zh | 罕见胃食管疾病 | |
| tr | Nadir gastroözofageal hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15111 | E | validated | |
| UMLS | C5681788 | E | validated | |
| GARD | 19786 | 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:97935Rare gastroenterologic disease
rare gastroenterological diseases
Children (14):
- ORPHA:2575Cystic fibrosis-gastritis-megaloblastic anemia syndrome
- ORPHA:2070Eosinophilic gastroenteritis
- ORPHA:2069Gastrocutaneous syndrome
- ORPHA:231080High-grade dysplasia in patients with Barrett esophagus
- ORPHA:930Idiopathic achalasia
- ORPHA:558411Idiopathic gastroparesis
- ORPHA:401945Moyamoya disease with early-onset achalasia
- ORPHA:2494Ménétrier disease
- ORPHA:329883Non-hypoproteinemic hypertrophic gastropathy
- ORPHA:2198Palmoplantar keratoderma-esophageal carcinoma syndrome
- ORPHA:487809Pediatric collagenous gastritis
- ORPHA:54028Plummer-Vinson syndrome
- ORPHA:180821Rare gastroesophageal tumor
- ORPHA:71272Sandifer syndrome
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/101936
- This record as JSON: /data/d/101936.json