vestibular ganglion 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 cell bodies, in the group of bipolar sensory nerve cell bodies concerned with equilibration that form a swelling on the vestibular part of the eighth cranial nerve in the fundus of the internal acoustic meatus (Mammalian Phenotype Ontology, MP_0006409)
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3 gene mutations causing the vestibular ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
MYO7A myosin VIIA
TBX10 T-box 10