| Label | Id | |
|---|---|---|
| combined oxidative phosphorylation deficiency caused by mutation in MIPEP | 14976 | |
| combined oxidative phosphorylation deficiency type 31 | 14976 | |
| lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome | 14976 | |
| amyotrophic lateral sclerosis | 4976 |