absent esophagus Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the part of the digestive canal through which food passes from the pharynx to the stomach (Mammalian Phenotype Ontology, MP_0004544)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004544
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1 gene mutations causing the absent esophagus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRD chordin