ORPHA:649029
Isolated left bronchial isomerism
Synonyms: Left bronchial isomerism without heterotaxy
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- Adult, Elderly
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated left bronchial isomerism | Left bronchial isomerism without heterotaxy |
| fr | Isomérisme bronchique gauche isolé | Isomérisme isolé gauche sans hétérotaxie |
| de | Isolierte Linksisomerie des Bronchialbaums | Linksbronchiale Isomerie ohne Heterotaxie |
| es | Isomería bronquial izquierda aislada | Isomería bronquial izquierda sin heterotaxia |
| it | Isomerismo bronchiale sinistro isolato | Isomerismo bronchiale sinistro senza eterotassia |
| nl | Geïsoleerde isomerie van linker bronchus | Isomerie van linker bronchus zonder heterotaxie |
| pt | Isomerismo brônquico isolado à esquerda | Isomerismo brônquico esquerdo sem heterotaxia |
| pl | Izolowana izomeria lewego oskrzela | = en |
| cs | Izolovaná izomerie levého bronchu | = en |
| uk | Ізольована ізомерія лівого бронха | Ізомерія лівого бронха без гетеротаксису |
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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 | 0958269 | E | validated | |
| MONDO | 958269 | E | validated | |
| UMLS | C5816741 | 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:649014Bronchial malformation
rare developmental anomalies during embryogenesis; rare respiratory diseases; rare surgical thoracic diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 4 cases | Worldwide | Case(s) | Validated | 33061133[PMID]_16633755[PMID]_36832240[PMID]_32481391[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 33061133[PMID]_16633755[PMID]_36832240[PMID]_32481391[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.
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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/649029
- This record as JSON: /data/d/649029.json