Summary

Oculoauricular Syndrome, also known as schorderet-munier-franceschetti syndrome,is related to microtia-anotia and cataract,and has symptoms including microcornea, rod-cone dystrophy and cataract. An important gene associated with Oculoauricular Syndrome is HMX1 (H6 Family Homeobox 1). Affiliated tissues include eye, and related mousephenotypes are hearing/vestibular/ear and behavior/neurological

All SNPs

Disease Hierarchy

Processes Associated With Trait

Symptoms Associated With Trait