Feingold syndrome type 2 (FS2) is a rare inherited malformation syndrome characterized by skeletal abnormalities and mild intellectual disabilities similar to those seen in Feingold syndrome type 1 (FS1) but that lacks the manifestations of gastrointestinal atresia and short palpebral fissures. The disease is MONDO_0013691 (Feingold syndrome type 2). Also known as: Brunner-Winter syndrome type 2, FGLDS2, FS2, MMT type 2, brachydactyly-short stature-microcephaly syndrome, microcephaly-digital anomalies-normal intelligence syndrome type 2, microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2.