2q37 microdeletion syndrome (MONDO_0010886) is a chromosomal anomaly involving deletion of chromosome band 2q37 and manifests as three major clinical findings: developmental delay, skeletal malformations and facial dysmorphism. Also known as: 2q37 monosomy, Albright hereditary osteodystrophy type 3, Albright hereditary osteodystrophy-like syndrome, BDMR, Del(2)(q37), brachydactyly intellectual disability syndrome, brachydactyly mental retardation syndrome, brachydactyly-intellectual disability syndrome.