All terms in MONDO
| Label | Id | Description |
|---|---|---|
| spinocerebellar ataxia type 41 | MONDO_0014626 | |
| developmental and epileptic encephalopathy, 33 | MONDO_0014625 | |
| Brown syndrome | MONDO_0014624 | |
| microcephaly 14, primary, autosomal recessive | MONDO_0014623 | |
| glossopharyngeal nerve neoplasm | MONDO_0002638 | |
| idiopathic granulomatous myositis | MONDO_0002644 | |
| cerebritis | MONDO_0002645 | |
| viral laryngitis | MONDO_0002646 | |
| optic nerve neoplasm | MONDO_0002640 | |
| subclavian artery aneurysm | MONDO_0002641 | |
| trochlear nerve neoplasm | MONDO_0002642 | |
| trochlear nerve disorder | MONDO_0007002 | |
| vestibular disorder | MONDO_0002643 | |
| trichothiodystrophy 3, photosensitive | MONDO_0014619 | |
| retinitis pigmentosa 71 | MONDO_0014618 | |
| intellectual disability, autosomal dominant 38 | MONDO_0014617 | |
| obsolete Skint1-like pseudogene | MONDO_0014616 | |
| myoclonic-atonic epilepsy | MONDO_0014633 | |
| hypomyelinating leukodystrophy 10 | MONDO_0014632 | |
| hypomagnesemia, seizures, and intellectual disability | MONDO_0014631 |