| Label | Id | |
|---|---|---|
| ocular, type i albinism | C537863 | |
| acyltransferase deficiency, lecithin:cholesterol | D007863 | |
| nettleship-falls type ocular albinism | C537863 | |
| congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and skeletal-spinal abnormalities | C567863 | |
| Kleine Levin syndrome | 7863 | |
| Kleine-LEVIN hibernation syndrome | 7863 | |
| familial Kleine-Levin syndrome | 7863 | |
| familial hibernation syndrome | 7863 | |
| albinism, ocular, type i | C537863 |