Infantile-onset recurrent acute liver failure and skeletal abnormalities

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Subtype of: Infantile liver failure · Liver failure
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
infantile-onset recurrent acute liver failure and skeletal abnormalities
MONDO_0032844
RINT1 Unknown
31204009
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Infantile-onset recurrent acute liver failure and skeletal abnormalities.
5 View disease cluster →
Infantile liver failure 1 shared geneRINT1 Related via 1 shared gene including RINT1. Skeletal abnormalities 1 shared geneRINT1 Related via 1 shared gene including RINT1. Short stature 1 shared geneRINT1 Related via 1 shared gene including RINT1. Hereditary breast cancer 1 shared geneRINT1 Related via 1 shared gene including RINT1. Liver failure 1 shared geneRINT1 Related via 1 shared gene including RINT1.