Complex lethal osteochondrodysplasia

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Subtype of: Osteochondrodysplasias
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
complex lethal osteochondrodysplasia
MONDO_0014821
TAPT1 Causal
26365339
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Complex lethal osteochondrodysplasia.
5 View disease cluster →
Osteochondrodysplasia, complex lethal, symoens-barnes-gistelinck type 1 shared geneTAPT1 Related via 1 shared gene including TAPT1. Osteochondrodysplasias 1 shared geneTAPT1 Related via 1 shared gene including TAPT1. Osteogenesis imperfecta 1 shared geneTAPT1 Related via 1 shared gene including TAPT1. Bone fragility with contractures, arterial rupture, and deafness 1 shared geneTAPT1 Related via 1 shared gene including TAPT1. Osteoporosis-pseudoglioma syndrome 1 shared geneTAPT1 Related via 1 shared gene including TAPT1.