Autosomal Dominant Myopia-Midfacial Retrusion-Sensorineural Hearing Loss-Rhizomelic Dysplasia Syndrome

Autosomal Dominant Myopia-Midfacial Retrusion-Sensorineural Hearing Loss-Rhizomelic Dysplasia Syndrome, is also known as autosomal dominant myopia-midfacial retrusion-sensorineural deafness-rhizomelic dysplasia syndrome. An important gene associated with Autosomal Dominant Myopia-Midfacial Retrusion-Sensorineural Hearing Loss-Rhizomelic Dysplasia Syndrome is COL11A1 (Collagen Type XI Alpha 1 Chain). Affiliated tissues include bone, and related phenotypes are cleft palate and micrognathia