Skeletal malformations syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
WNT7A- related skeletal malformations syndrome
MONDO_0009232
WNT7A Unknown
16826533 20949531 21271649 21344627 7885472 9128926
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Skeletal malformations syndrome.
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Fuhrmann syndrome 1 shared geneWNT7A Related via 1 shared gene including WNT7A. Limb/pelvis-hypoplasia/aplasia syndrome 1 shared geneWNT7A Related via 1 shared gene including WNT7A. Urogenital neoplasms 1 shared geneWNT7A Related via 1 shared gene including WNT7A. Synovitis, acne, pustulosis, hyperostosis, and osteitis 1 shared geneWNT7A Related via 1 shared gene including WNT7A. Bladder exstrophy and epispadias complex 1 shared geneWNT7A Related via 1 shared gene including WNT7A.