Larsen syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
LARSEN SYNDROME
C0175778150250503MONDO:0007875
CHST3 Causal — Disgenet
FGFR3 Causal — Disgenet
FLNB Causal — ClinVar, Disgenet, GenCC, HPO, Orphanet
LARSEN-LIKE SYNDROME, B3GAT3 TYPE
284139MONDO:0009511
B3GAT3 Causal
20164147 21763480 245816 24668659 25893793 26086840 27871226 29318063 31196143 495764
ClinVar, GWAS catalog, Orphanet
All17 Causal4 Unknown16
Related Diseases Diseases that share the most curated genes with Larsen syndrome.
5 View disease cluster →
Bone fragility with contractures, arterial rupture, and deafness 9 shared genesGORAB, XYLT1, P4HA1, CHST3, XYLT2, B3GALT6, B3GAT3, B4GALT7, PLOD3 Related via 9 shared genes including GORAB, XYLT1, P4HA1. Osteoporosis-pseudoglioma syndrome 9 shared genesGORAB, XYLT1, P4HA1, CHST3, XYLT2, B3GALT6, B3GAT3, B4GALT7, PLOD3 Related via 9 shared genes including GORAB, XYLT1, P4HA1. Desbuquois dysplasia 2 shared genesXYLT1, CANT1 Related via 2 shared genes including XYLT1, CANT1. Pseudoxanthoma elasticum 2 shared genesXYLT1, XYLT2 Related via 2 shared genes including XYLT1, XYLT2. Marshall syndrome 3 shared genesXYLT2, PLOD3, GZF1 Related via 3 shared genes including XYLT2, PLOD3, GZF1.