UCP2 and Neurodevelopmental delay: This region contains five genes, with C2CD3, DNAJB13, and UCP2 involved in six phenotypes of the nervous system including abnormality of nervous system physiology (HP:0012638), abnormality of nervous system (HP:0000707), neurodevelopmental abnormality (HP:0012759), neurodevelopmental delay (HP:0012758), morphological abnormality of the central nervous system (HP:0002011), and abnormality of nervous system morphology (HP:0012639).