Preferred Name | Esophageal_Atresia | |
Synonyms |
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ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Esophageal_Atresia |
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ID |
C87072 |
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NCI_Definition |
A congenital abnormality of the esophagus in which the upper esophagus ends as a blind pouch and does not connect with the lower esophagus; it is often accompanied by a tracheoesophageal fistula. Signs and symptoms in a newborn with this abnormality include excessive salivation, choking, coughing, and the development of cyanosis and respiratory distress when fed. |
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NCI_PT |
Esophageal Atresia |
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NICHD_Definition |
_ |
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prefixIRI |
Esophageal_Atresia |
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prefLabel |
Esophageal_Atresia |
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Subset_Association1 |
NICHD Pediatric Terminology |
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Subset_Association2 |
Neonatal Research Network Terminology |
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SYN |
Congenital Atresia of Esophagus |
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subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Abnormality_of_the_Digestive_System |
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