Summary

46 Cousin syndrome is a rare syndrome characterized mainly by short stature at birth, unusual facial appearance and skeletal abnormalities involving the shoulder blades and hips. intelligence may vary from normal to moderately delayed. mutations in the tbx15 gene inherited in an autosomal recessive pattern have been suggested as the cause of this condition

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Symptoms Associated With Trait