Marshall syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MARSHALL SYNDROME
154780560C0265235MESH:C536025MONDO:0007949
COL11A1 Causal
25073711 17236192 10486316 9529347 22499343
CTD, ClinVar, Disgenet, GWAS catalog, HPO, Orphanet
All19 Causal1 Unknown18
Related Diseases Diseases that share the most curated genes with Marshall syndrome.
5 View disease cluster →
Stickler syndrome 10 shared genesCOL2A1, COL11A1, BMP4, LRP2, VCAN, COL11A2, COL9A1, COL9A2, COL9A3, LOXL3 Related via 10 shared genes including COL2A1, COL11A1, BMP4. Epiphyseal dysplasia 5 shared genesSLC26A2, COL2A1, COL9A1, COL9A2, COL9A3 Related via 5 shared genes including SLC26A2, COL2A1, COL9A1. Congenital cartilage disorder 7 shared genesSLC26A2, COL2A1, COL11A1, COL11A2, COL9A1, COL9A2, COL9A3 Related via 7 shared genes including SLC26A2, COL2A1, COL11A1. Osteochondrodysplasias 7 shared genesSLC26A2, COL2A1, COL11A1, COL11A2, COL9A1, COL9A2, COL9A3 Related via 7 shared genes including SLC26A2, COL2A1, COL11A1. Intervertebral disc disease 3 shared genesCOL11A1, COL9A2, COL9A3 Related via 3 shared genes including COL11A1, COL9A2, COL9A3.