ORPHA:649010
Non-syndromic congenital bronchial atresia
Synonyms: Non-syndromic CBA
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- Adult
- 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 congenital bronchial atresia | Non-syndromic CBA |
| fr | Atrésie bronchique congénitale non syndromique | |
| de | Nicht-syndromale kongenitale Bronchialatresie | Nicht-syndromale CBA |
| es | Atresia bronquial congénita no sindrómica | ABC no sindrómica |
| it | Atresia bronchiale congenita non sindromica | CBA non sindromica |
| nl | Niet-syndromale congenitale atresie van bronchus | Niet-syndromale CBA · Niet-syndromale congenitale bronchusatresie |
| pt | Atrésia brônquica congénita não-sindrómica | CBA não-sindrómico |
| pl | Niesyndromiczka wrodzona atrezja oskrzela | = en |
| cs | Nesyndromická vrozená bronchiální atrézie | = en |
| uk | Несиндромальна вроджена атрезія бронхів | Несиндромальний CBA |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q32.4 | NTBT | inclusion | validated |
| ICD-11 | LA74.0 | NTBT | index | validated |
| MONDO | 0958268 | E | validated | |
| MONDO | 958268 | E | validated | |
| UMLS | C5816738 | 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
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | — | Worldwide | Class only | Validated | 15366333[PMID] |
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/649010
- This record as JSON: /data/d/649010.json