pharynx hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, of the passage between the mouth and the posterior nares and the larynx and esophagus (Mammalian Phenotype Ontology, MP_0004555)
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2 gene mutations causing the pharynx hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
NKX2-5 NK2 homeobox 5
TBX1 T-box 1