absent epiglottis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing the most superior of the laryngeal cartilages, which is normally found at the root of the tongue and folds back over the entrance to the larynx during swallowing, preventing inhalation of food or drink (Mammalian Phenotype Ontology, MP_0013261)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013261
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Genes

1 gene mutations causing the absent epiglottis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXC1 forkhead box C1