All terms in MONDO
| Label | Id | Description |
|---|---|---|
| optic pathway glioma | MONDO_0016167 | |
| visual pathway disorder | MONDO_0001834 | |
| bilateral frontal polymicrogyria | MONDO_0016162 | |
| bilateral polymicrogyria | MONDO_0017091 | |
| autosomal dominant cerebellar ataxia type II | MONDO_0016163 | |
| herpetiform pemphigus | MONDO_0016164 | |
| X-linked intellectual disability-epilepsy syndrome | MONDO_0016160 | |
| cerebral gigantism-jaw cysts syndrome | MONDO_0016161 | |
| obsolete rare bone disease related to a common gene or pathway defect | MONDO_0031799 | |
| iris spindle cell melanoma | MONDO_0004188 | |
| spindle cell intraocular melanoma | MONDO_0003744 | |
| iris melanoma | MONDO_0004064 | |
| nodular fasciitis | MONDO_0004187 | |
| fasciitis | MONDO_0004830 | |
| esophageal tuberculosis | MONDO_0004189 | |
| spinal cord injury | MONDO_0043797 | |
| spinal injury | MONDO_0037747 | |
| axonal neuropathy | MONDO_0004183 | |
| cranial nodular fasciitis | MONDO_0004186 | |
| ovarian serous cystadenofibroma | MONDO_0004185 |