Osteogenesis imperfecta type 3

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Subtype of: Osteogenesis imperfecta
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
OI3
MONDO_0009804
SERPINH1 Unknown
20188343 25510505
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Osteogenesis imperfecta type 3.
5 View disease cluster →
Preterm premature rupture of the membranes, susceptibility to 1 shared geneSERPINH1 Related via 1 shared gene including SERPINH1. Osteogenesis imperfecta 1 shared geneSERPINH1 Related via 1 shared gene including SERPINH1. Skeletal dysplasia 1 shared geneSERPINH1 Related via 1 shared gene including SERPINH1. Bone fragility with contractures, arterial rupture, and deafness 1 shared geneSERPINH1 Related via 1 shared gene including SERPINH1. Osteoporosis-pseudoglioma syndrome 1 shared geneSERPINH1 Related via 1 shared gene including SERPINH1.