absent styloid process Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the slender needle-like pointed projection that runs downward and slightly forward from the base of the inferior surface of the petrous portion of the temporal bone to join the tympanic portion (Mammalian Phenotype Ontology, MP_0008386)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008386
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Genes

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

Symbol Name
HOXA2 homeobox A2