pterygoid bone 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 cells, in the bone region which corresponds to the inner plate of the pterygoid process of the mammalian skull (Mammalian Phenotype Ontology, MP_0004455)
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2 gene mutations causing the pterygoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MN1 meningioma (disrupted in balanced translocation) 1
PRRX1 paired related homeobox 1