MONDO_0007219 (Osebold-Remondini syndrome) is a brachymesophalangy with mesomelic short limbs, and carpal and tarsal bone abnormalities. In general, the affected individuals are of slightly short stature and normal intelligence. The syndrome has been described in a kindred with seven affected members from three generations. Transmission appears to be autosomal dominant. Also known as: BDA6, brachydactyly type A6, brachydactyly, type A6, brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities.