palatine bone horizontal plate hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment, usually due to a deficiency in the number of cells, of the bony plate of the palatine bone that normally fuses with maxillary shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0009896)
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1 gene mutations causing the palatine bone horizontal plate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MN1 meningioma (disrupted in balanced translocation) 1