Summary

Riddle Syndrome, also known as rnf168 deficiency,is related to canavan disease and exhibitionism,and has symptoms including microcephaly, pulmonary fibrosis and dry skin. An important gene associated with Riddle Syndrome is RNF168 (Ring Finger Protein 168), and among its related pathways are ATM Pathway and SUMOylation. Affiliated tissues include skin and colon, and related mousephenotype neoplasm

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Symptoms Associated With Trait