raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:280205

Laryngotracheoesophageal cleft type 0

Synonyms: LTEC0 · Laryngo-tracheo-esophageal cleft type 0

Type
Clinical subtype
Group
Subtype of disorder
Status
active

Laryngo-tracheo-esophageal cleft (LC) type 0 is a congenital respiratory tract anomaly characterized by a submucosal laryngo-tracheo-esophageal cleft with minor symptoms or an asymptomatic course.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enLaryngotracheoesophageal cleft type 0LTEC0 · Laryngo-tracheo-esophageal cleft type 0
frFente laryngo-trachéo-oesophagienne type 0LTEC0
deLaryngo-tracheo-ösophageale Spalte Typ 0LTEC0
esHendidura laringotraqueoesofágica tipo 0Hendidura laringo-traqueo-esofágica tipo 0 · LTEC0
itSchisi laringo-tracheo-esofagea, tipo 0LTEC0
nlLaryngo-tracheo-oesofageale fissuur type 0LTEC0
ptFenda laringo-traqueo-esofágica tipo 0LTECO
plSzczelina krtaniowo-tchawiczo-przełykowa typu 0LTEC0
csLaryngotracheoezofageální rozštěp, typ 0LTEC0
ukЛаринготрахеостравохідна розщілина, тип 0Ларинго-трахео-стравохідна щілина 0 типу · LTEC0
zh喉气管食道裂0型0型喉-气管-食道裂
trLaringotrakeoözofageal yarık tip 0LTEC0 · Laringo-trakeo-özofageal yarık tip 0

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q32.1NTBTattributedvalidated
ICD-11LA72NTBTindexvalidated
MONDO0017220Evalidated
UMLSC5438977Evalidated

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 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

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