Fuhrmann syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Fuhrmann syndrome
MONDO_0009232
WNT7A Causal
16826533 21271649 9128926 21344627 20949531
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Fuhrmann syndrome.
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Skeletal malformations 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.