Ring chromosome 9

Ring chromosome 9 syndrome is an autosomal anomaly characterized by variable clinical features, most commonly including developmental delay, some degree of intellectual disability, facial dysmorphism, microcephaly, congenital heart anomalies, and variable genital, limb and skeletal anomalies.

Also known as: Chromosome 9 Ring, Ring 9, Ring chromosome type 9, Ring chromosome 9 syndrome, chromosome 9 ring, r9

0 clinical trials for this condition and its sub-types, 0 tagged with Ring chromosome 9 itself.