alisphenoid bone hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size in either of the broad curved wing like expanses on each side of the sphenoid bone in adults, usually due to reduced cell number; this bone may exist independently in the young (Mammalian Phenotype Ontology, MP_0004460)
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4 gene mutations causing the alisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ECE1 endothelin converting enzyme 1
MN1 meningioma (disrupted in balanced translocation) 1
PRRX1 paired related homeobox 1
PTCH1 patched 1