ORPHA:93940
Laryngotracheoesophageal cleft type 3
Synonyms: LTEC III · LTEC3 · Laryngo-tracheo-esophageal cleft type 3
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Age of onset
- Infancy, Neonatal
- Status
- active
A congenital respiratory tract anomaly characterized by a cleft extending through the cricoid cartilage, sometimes into the cervical trachea, with severe swallowing disorders, lung infections and pulmonary damage.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Laryngotracheoesophageal cleft type 3 | LTEC III · LTEC3 · Laryngo-tracheo-esophageal cleft type 3 |
| fr | Fente laryngo-trachéo-oesophagienne type 3 | LTEC III · LTEC3 |
| de | Laryngo-tracheo-ösophageale Spalte Typ 3 | LTEC III · LTEC3 |
| es | Hendidura laringotraqueoesofágica tipo 3 | Hendidura laringo-traqueo-esofágica tipo 3 · LTEC III · LTEC3 |
| it | Schisi laringo-tracheo-esofagea, tipo 3 | LTEC III · LTEC3 |
| nl | Laryngo-tracheo-oesofageale fissuur type 3 | LTEC III · LTEC3 |
| pt | Fenda laringotraqueoesofágica tipo 3 | |
| pl | Rozszczep krtaniowo-tchawiczo-przełykowy typu 3 | LTEC3 · LTEC III |
| cs | Laryngotracheoezofageální rozštěp, typ 3 | LTEC III · LTEC3 |
| uk | Ларинготрахеостравохідна розщілина, тип 3 | Ларинго-трахео-стравохідна щілина 3 типу · LTEC III · LTEC3 |
| zh | 喉气管食管裂3型 | 喉-气管-食管裂3型 |
| tr | Laringotrakeoözofageal yarık tip 3 | LTEC3 · LTEC III · Laringo-trakeo-özofageal yarık tip 3 |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 215800 | BTNT | validated | |
| ICD-10 | Q32.1 | NTBT | attributed | validated |
| ICD-11 | LA72 | NTBT | index | validated |
| MONDO | 0019763 | E | validated | |
| UMLS | C0584825 | 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: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.
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 | 30 cases | Worldwide | Case(s) | Validated | [EXPERT] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | 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.
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/93940
- This record as JSON: /data/d/93940.json