Esophageal Atresia (CEA)

Alias:
Oesophageal Atresia
Esophageal Atresia with or Without Trachea-Esophageal Fistula
Congenital Imperforate Esophagus
Congenital Atresia of Esophagus
Congenital Esophageal Atresia
Imperforate Esophagus
Ea/tef
Cea
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Esophageal Atresia, also known as oesophageal atresia, is related to vater/vacterl association and microphthalmia, syndromic 3. An important gene associated with Esophageal Atresia is TENT5A (Terminal Nucleotidyltransferase 5A), and among its related pathways/superpathways are Gastrulation and Signaling by Hedgehog. The drugs Omeprazole and Gastrointestinal Agents have been mentioned in the context of this disorder. Affiliated tissues include trachea and lung, and related phenotypes are tracheoesophageal fistula and dysphagia
Related ID:
MESH:D004933

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Newborn
1-9/100000
27
340
--

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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