hyoid bone hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment of the hyoid bone, usually due to a deficiency in the number of cells (Mammalian Phenotype Ontology, MP_0009899)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009899
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3 gene mutations causing the hyoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRD chordin
RUNX2 runt-related transcription factor 2
WNT9A wingless-type MMTV integration site family, member 9A