ORPHA:662405
Isolated pyloric duplication
Synonyms: Congenital isolated double pylorus · Isolated duplication cyst of the pyloric canal · Isolated duplication cyst of the pylorus
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated pyloric duplication | Congenital isolated double pylorus · Isolated duplication cyst of the pyloric canal · Isolated duplication cyst of the pylorus |
| fr | Duplication pylorique isolée | Duplication isolée du canal pylorique · Duplication isolée du pylor |
| de | Pylorus-Duplikation, isolierte | Isolierte Duplikationszyste des Pylorus · Isolierte kongenitale Verdoppelung des Pylorus · IsolierteDuplikationszyste des Pyloruskanals |
| es | Duplicación pilórica aislada | Píloro doble congénito aislado · Quiste de duplicación aislado del canal pilórico · Quiste de duplicación aislado del píloro |
| it | Duplicazione del piloro | Cisti da duplicazione del canale pilorico · Cisti da duplicazione del piloro · Doppio piloro congenito |
| nl | Geïsoleerde duplicatie van pylorus | Congenitale geïsoleerde dubbele pylorus · Geïsoleerde duplicatiecyste van pylorus · Geïsoleerde duplicatiecyste van pyloruskanaal · Geïsoleerde duplicatuur van pylorus |
| pt | Duplicação pilórica isolada | Piloro duplo congénito isolado · Quisto de duplicação do canal pilórico isolado · Quisto de duplicação do piloro isolado |
| pl | Isolated pyloric duplication | = en |
| cs | Duplikace pyloru | = en |
| uk | Пілоричне подвоєння | Вроджений подвійний пілорус · Кіста дублювання пілоричного каналу · Кіста дублювання пілоруса |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q40.2 | NTBT | attributed | validated |
| UMLS | C5925069 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:108963Non-syndromic gastroduodenal malformation
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 18 cases | Worldwide | Case(s) | Validated | 24426605[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 24426605[PMID]_ORPHANET |
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
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/662405
- This record as JSON: /data/d/662405.json