absent endolymphatic sac Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the dilated blind extremity of the endolymphatic duct, which lies external to the dura on the posterior aspect of the petrous part of the temporal bone (Mammalian Phenotype Ontology, MP_0006013)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006013
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2 gene mutations causing the absent endolymphatic sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGF3 fibroblast growth factor 3
HOXA1 homeobox A1