Skeletal abnormalities

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
skeletal abnormalities
HP:0000924
FICD Unknown
36704923
Open Targets —
RINT1 Unknown
31204009
Open Targets
RNU4ATAC Unknown
41864208
Open Targets —
RNU6ATAC Unknown
41864208
Open Targets —
All4 Causal0 Unknown4
Related Diseases Diseases that share the most curated genes with Skeletal abnormalities.
5 View disease cluster →
Growth failure 2 shared genesRNU4ATAC, RNU6ATAC Related via 2 shared genes including RNU4ATAC, RNU6ATAC. Hepatic disease 2 shared genesRNU4ATAC, RNU6ATAC Related via 2 shared genes including RNU4ATAC, RNU6ATAC. Infantile-onset recurrent acute liver failure and skeletal abnormalities 1 shared geneRINT1 Related via 1 shared gene including RINT1. Severe neurodevelopmental delay 1 shared geneFICD Related via 1 shared gene including FICD. Spastic paraplegia 92, autosomal recessive 1 shared geneFICD Related via 1 shared gene including FICD.