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Mammalian Phenotype Browser
Term Detail
MP term:esophageal atresia
Synonym: esophageal narrowing
MP id: MP:0003276
Alternate id: Fyler:4412
Definition: congenital blockage or absence of the lumen of the esophagus
Number of paths to term: 1

is-adenotes an 'is-a' relationship
part-ofdenotes a 'part-of' relationship


mammalian phenotype
        is-adigestive/alimentary phenotype
                is-aabnormal digestive system morphology
                        is-aabnormal esophagus morphology
                                is-aabnormal esophageal development
                                is-aabnormal esophageal epithelium morphology +
                                is-aabnormal esophageal smooth muscle morphology
                                is-aabsent esophagus
                                is-adilated esophagus
                                is-aenlarged esophagus +
                                is-aesophageal atresia [MP:0003276] (6 genotypes, 6 annotations)
                                is-aesophageal ulcer
                                is-aesophagogastric junction metaplasia
                                is-aesophagus stenosis
                                is-asmall esophagus +
                                is-atracheoesophageal fistula

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Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/18/2014
MGI 5.20
The Jackson Laboratory