craniofacial asymmetry Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Asymmetry of the bones of the skull and the face. (Human Phenotype Ontology, HP_0004484)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008863
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Genes

1 gene mutations causing the craniofacial asymmetry phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFR1 fibroblast growth factor receptor 1