Fg syndrome 2

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Subtype of: Fg syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Fg syndrome type 2
MONDO_0010297
FLNA Unknown
10982965 11532987 11914408 12612583 14988809 15654694 15940695 16299064 16596676 17431908 17632775 18854860 20014127 20301567 23032111 23037936 23934111 28425981 28498505 30712878 8290091 8644737 9883725
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Fg syndrome 2.
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Otopalatodigital spectrum disorder 1 shared geneFLNA Related via 1 shared gene including FLNA. Terminal osseous dysplasia with pigmentary defects 1 shared geneFLNA Related via 1 shared gene including FLNA. X-linked ehlers-danlos syndrome 1 shared geneFLNA Related via 1 shared gene including FLNA. X-linked keloid scarring syndrome 1 shared geneFLNA Related via 1 shared gene including FLNA. Melnick-needles syndrome 1 shared geneFLNA Related via 1 shared gene including FLNA.