cortical irregularity Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal irregularity of cortical bone. (Human Phenotype Ontology, HP_0005731)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005731
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Genes

2 genes associated with the cortical irregularity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
SH3PXD2B SH3 and PX domains 2B