ORPHA:280821
Communicating congenital bronchopulmonary-foregut malformation
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Communicating congenital bronchopulmonary-foregut malformation | |
| fr | Malformation congénitale broncho-pulmonaire communiquant avec l'intestin antérieur | |
| de | Kommunizierende kongenitale bronchopulmonale Missbildung des Vorderdarms | |
| es | Malformación congénita broncopulmonar comunicante con el intestino anterior | |
| it | Malformazione broncopolmonare congenita comunicante con l'intestino anteriore | |
| nl | Communicerende congenitale bronchopulmonale voordarmmalformatie | |
| pt | Malformação congénita de comunicação broncopulmonar-digestiva | |
| pl | Wrodzona komunikująca malformacja oskrzelowo-płucna i jelita przedniego | |
| cs | Plicní sekvestrace komunikující s gastrointestinálním traktem | Vrozená bronchopulmonální malformace komunikující s předním střevem |
| uk | Комунікативна вроджена бронхо-легенево-шлунково-кишкова вада розвитку | |
| zh | 交通性先天性支气管肺-前肠畸形 | |
| tr | Doğumsal bronkopulmoner-ön bağırsak malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q33.2 | NTBT | attributed | validated |
| ICD-11 | LA75.6 | NTBT | attributed | validated |
| MONDO | 0017247 | E | validated | |
| UMLS | C0265790 | 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:3161Congenital pulmonary sequestration
rare developmental anomalies during embryogenesis; rare respiratory diseases; rare surgical thoracic diseases
No children.
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/280821
- This record as JSON: /data/d/280821.json