All terms in MONDO
| Label | Id | Description |
|---|---|---|
| cranial nerve palsy | MONDO_0002782 | |
| riboflavin transporter deficiency | MONDO_0008891 | |
| Koolen-de Vries syndrome due to a point mutation | MONDO_0018217 | |
| Koolen-de Vries syndrome | MONDO_0012496 | |
| Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome | MONDO_0018216 | |
| partial deletion of the long arm of chromosome 17 | MONDO_0016915 | |
| MONDO_0018219 | MONDO_0018219 | |
| autosomal recessive cerebral atrophy | MONDO_0018218 | |
| hereditary sensory and autonomic neuropathy type 1 | MONDO_0018213 | |
| familial cervical artery dissection | MONDO_0018212 | |
| cervical artery dissection | MONDO_0006061 | |
| Aloi Tomasini Isaia syndrome | MONDO_0021845 | |
| generalized epilepsy with febrile seizures plus | MONDO_0018214 | |
| obsolete alopecia macular degeneration growth retardation syndrome | MONDO_0021849 | |
| Balint syndrome | MONDO_0018211 | |
| simultanagnosia | MONDO_0000678 | |
| Alexander disease type II | MONDO_0018210 | |
| head and neck paraganglioma | MONDO_0006239 | |
| paraganglioma | MONDO_0000448 | |
| alopecia universalis onychodystrophy vitiligo | MONDO_0021851 |