bifid sacrum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Presence of a bifid sacral bone. (Human Phenotype Ontology, HP_0009791)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009791
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Genes

1 genes associated with the bifid sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MNX1 motor neuron and pancreas homeobox 1