Interestingly, PHOX2B common variants resulted in a cumulative frequency higher in a set of children affected by obstructive sleep apnea (OSA) with class III malocclusion than in controls (33), an observation that further supports the role of the PHOX2B gene in respiratory disorders beyond CCHS, as suggested by OSA occurrence in infants of families with multiple histories of SIDS and ALTE (34). The gene discussed is PHOX2B; the disease is respiratory system disorder.