ORPHA:648992
Non-syndromic bridging bronchus
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- Antenatal, Infancy, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic bridging bronchus | |
| fr | Bridging bronchus non syndromique | |
| de | Bridging-Bronchus, nicht syndromaler | |
| es | Bronquio puente no sindrómico | |
| it | Bronco a cavaliere non sindromico | |
| nl | Niet-syndromale 'bridging bronchus' | |
| pt | Brônquio ponte não-sindrómico | |
| pl | Niesyndromiczna anomalia rozgałęzienia oskrzela | |
| cs | Nesyndromický přemosťující bronchus | |
| uk | Несиндромальний перемикаючий бронх |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q32.4 | NTBT | attributed | validated |
| ICD-11 | LA74.Y | NTBT | attributed | validated |
| MONDO | 0958267 | E | validated | |
| MONDO | 958267 | E | validated | |
| UMLS | C5816737 | 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:649014Bronchial malformation
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
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 17 cases | Worldwide | Case(s) | Validated | 32534300[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 32534300[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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/648992
- This record as JSON: /data/d/648992.json