All terms in MONDO
| Label | Id | Description |
|---|---|---|
| disorder of peroxisomal beta oxidation | MONDO_0019233 | |
| hearing loss with skin disease | MONDO_0100113 | |
| dry age related macular degeneration | MONDO_0100114 | |
| acute flaccid myelitis | MONDO_0100115 | |
| Middle East respiratory syndrome | MONDO_0100116 | |
| Orthocoronavirinae infectious disease | MONDO_0020753 | |
| obsolete familial sudden death | MONDO_0100117 | |
| Knobloch syndrome 2 | MONDO_0100119 | |
| Knobloch syndrome | MONDO_0800166 | |
| SCN4A-related myopathy, autosomal recessive | MONDO_0100121 | |
| GNPTAB-mucolipidosis | MONDO_0100122 | |
| toxic bronchiolitis | MONDO_0100123 | |
| NAA10-related syndrome | MONDO_0100124 | |
| hallucinogen-persisting perception disorder | MONDO_0100125 | |
| P5CS deficiency | MONDO_0100126 | |
| inborn disorder of proline metabolism | MONDO_0017355 | |
| inborn disorder of ornithine metabolism | MONDO_0017356 | |
| toxic bronchiolitis obliterans | MONDO_0100127 | |
| coinfection | MONDO_0100128 | |
| intracranial arachoid cyst | MONDO_0100129 |