Larsen-like syndrome, b3gat3 type

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Subtype of: Larsen syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Larsen-like syndrome, B3GAT3 type
MONDO_0009511
B3GAT3 Causal
28771243 31196143 31438591
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Larsen-like syndrome, b3gat3 type.
5 View disease cluster →
Multiple joint dislocations, short stature, and craniofacial dysmorphism with or without congenital heart defects 1 shared geneB3GAT3 Related via 1 shared gene including B3GAT3. Larsen syndrome 1 shared geneB3GAT3 Related via 1 shared gene including B3GAT3. Bone fragility with contractures, arterial rupture, and deafness 1 shared geneB3GAT3 Related via 1 shared gene including B3GAT3. Osteoporosis-pseudoglioma syndrome 1 shared geneB3GAT3 Related via 1 shared gene including B3GAT3. Craniofacial abnormalities 1 shared geneB3GAT3 Related via 1 shared gene including B3GAT3.