Laryngo-tracheo-esophageal cleft type 3
General Information (adopted from Orphanet):
| Synonyms, Signs: |
LTEC III LTEC3 |
| Number of Symptoms | 7 |
| OrphanetNr: | 93940 |
| OMIM Id: |
215800
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| ICD-10: |
Q32.1 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
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| Age of onset: |
Neonatal Infancy [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Laryngo-tracheo-esophageal cleft
-Rare developmental defect during embryogenesis -Rare genetic disease -Rare otorhinolaryngologic disease -Rare respiratory disease -Rare surgical thoracic disease |
Symptom Information:
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(HPO:0000961) | Cyanosis | 60 / 7739 | ||||
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(HPO:0006511) | Laryngeal stridor | 6 / 7739 | ||||
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(HPO:0002835) | Aspiration | 11 / 7739 | ||||
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(MedDRA:10008589) | Choking | 6 / 7739 | ||||
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(OMIM) | Cleft larynx | 2 / 7739 | ||||
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(OMIM) | Persistent esophagotrachea | 2 / 7739 | ||||
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(OMIM) | Abnormal | 2 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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