ORPHA:231080
High-grade dysplasia in patients with Barrett esophagus
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | High-grade dysplasia in patients with Barrett esophagus | |
| fr | Dysplasie de haut grade chez les patients présentant un oesophage de Barrett | |
| de | Hochgradige Dysplasie in Patienten mit Barrett-Ösophagus | Hochgradigen Neoplasie der Barrett-Schleimhaut |
| es | Displasia de grado alto en pacientes con esófago de Barrett | |
| it | Displasia di alto grado nei pazienti affetti da esofago di Barrett | |
| nl | Hooggradige dysplasie bij patiënten met Barrett-oesofagus | |
| pt | Displasia de alto grau em doentes com esófago de Barrett | |
| pl | Dysplazja wysokiego stopnia u pacjentów z przełykiem Barreta | |
| cs | Těžká dysplázie u pacientů s Barretovým jícnem | |
| uk | Дисплазія високого ступеня у пацієнтів зі стравоходом Барретта | |
| zh | 患者高度发育异常伴巴雷特食管 | |
| tr | Barrett özofagusu ile seyreden hastalarda yüksek dereceli displazi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | K22.7 | NTBT | attributed | validated |
| ICD-11 | DA23.1 | NTBT | index | validated |
| UMLS | C1334003 | 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:101936Rare gastroesophageal disease
rare gastroenterological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-5 / 10 000 | 36 / 100 000 | Europe | Value and class | Validated | European Medicines Agency 2002[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
4 annotations · validated 2023-08-21| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0100580 | Barrett esophagus | |
| Frequent (79-30%) | ||
| HP:0002015 | Dysphagia | |
| HP:0002020 | Gastroesophageal reflux | |
| Occasional (29-5%) | ||
| HP:0005240 | Esophageal obstruction | |
Run the differential on the 1 obligate / very frequent terms
Annotation source: 28613697[PMID]
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/231080
- This record as JSON: /data/d/231080.json