Genetics

Autosomal dominant hypocalcemia

GTF2H5 gene

Vibratory urticaria

Dopamine transporter deficiency syndrome

Microphthalmia

ELOVL4 gene

Gilbert syndrome

PRICKLE1-related progressive myoclonus epilepsy with ataxia

Pelizaeus-Merzbacher disease

VCAN gene

Opioid addiction

SCN9A gene