ORPHA:93939
Laryngotracheoesophageal cleft type 2
Synonyms: LTEC II · LTEC2 · Laryngo-tracheo-esophageal cleft type 2
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Age of onset
- Infancy, Neonatal
- Status
- active
A congenital respiratory tract anomaly characterized by a cleft extending below the vocal folds into the cricoid cartilage, with swallowing disorders and lung infections.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Laryngotracheoesophageal cleft type 2 | LTEC II · LTEC2 · Laryngo-tracheo-esophageal cleft type 2 |
| fr | Fente laryngo-trachéo-oesophagienne type 2 | LTEC II · LTEC2 |
| de | Laryngo-tracheo-ösophageale Spalte Typ 2 | LTEC II · LTEC2 |
| es | Hendidura laringotraqueoesofágica tipo 2 | Hendidura laringo-traqueo-esofágica tipo 2 · LTEC II · LTEC2 |
| it | Schisi laringo-tracheo-esofagea, tipo 2 | LTEC II · LTEC2 |
| nl | Laryngo-tracheo-oesofageale fissuur type 2 | LTEC II · LTEC2 |
| pt | Fenda laringotraqueoesofágica tipo 2 | |
| pl | Rozszczep krtaniowo-tchawiczo-przełykowy typu 2 | LTEC2 · LTEC II |
| cs | Laryngotracheoezofageální rozštěp, typ 2 | LTEC II · LTEC2 |
| uk | Ларинготрахеостравохідна розщілина, тип 2 | Ларинго-трахео-стравохідна щілина 2 типу · LTEC II · LTEC2 |
| zh | 喉气管食管裂2型 | 喉-气管-食管裂2型 |
| tr | Laringotrakeoözofageal yarık tip 2 | LTEC2 · LTEC II · Laringo-trakeo-özofageal yarık tip 2 |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q32.1 | NTBT | attributed | validated |
| ICD-11 | LA72 | NTBT | index | validated |
| MONDO | 0019762 | E | validated | |
| UMLS | C0584824 | 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:2004Laryngotracheoesophageal cleft
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical diseases; rare respiratory diseases; rare surgical thoracic diseases; rare otorhinolaryngological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | 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/93939
- This record as JSON: /data/d/93939.json