multiple prenatal fractures Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of bone fractures in the prenatal period that are diagnosed at birth or before. (Human Phenotype Ontology, HP_0005855)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005855
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Genes

6 genes associated with the multiple prenatal fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
CRTAP cartilage associated protein
LBR lamin B receptor
P3H1 prolyl 3-hydroxylase 1
PPIB peptidylprolyl isomerase B (cyclophilin B)