Summary

Raine Syndrome, also known as lethal osteosclerotic bone dysplasia,is related to microphthalmia microtia fetal akinesia and renal nutcracker syndrome,and has symptoms including microcephaly, micrognathia and low-set, posteriorly rotated ears. An important gene associated with Raine Syndrome is FAM20C (FAM20C, Golgi Associated Secretory Pathway Kinase). Affiliated tissues include bone, eye and tongue, and related mousephenotypes are skeleton and renal/urinary system

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Symptoms Associated With Trait