Monarch Disease Ontology id MONDO_0010026 (SHORT syndrome) is a rare disorder characterized by multiple congenital anomalies, including short stature, hyperextensibility of joints, ocular depression, Rieger anomaly and teething delay in which the cause of the disease is a mutation in PIK3R1 gene. Other common manifestations of SHORT syndrome are mild intrauterine growth restriction, partial lipodystrophy, delayed bone age, hernias and a recognizable facial gestalt. Also known as: Aarskog-Ose-Pande syndrome, Rieger anomaly-partial lipodystrophy syndrome, lipodystrophy-Rieger anomaly-diabetes syndrome, short syndrome.