All terms in MONDO
| Label | Id | Description |
|---|---|---|
| peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain | MONDO_0009851 | |
| nanophthalmos 1 | MONDO_0010836 | |
| periodontitis, chronic, adult | MONDO_0009850 | |
| autosomal dominant congenital benign spinal muscular atrophy | MONDO_0010839 | |
| gonadal agenesis | MONDO_0010838 | |
| congenital arteriovenous shunt | MONDO_0022819 | |
| Lowry-MacLean syndrome | MONDO_0010851 | |
| Tessier number 4 facial cleft | MONDO_0010850 | |
| oculomaxillofacial dysostosis | MONDO_0015824 | |
| oblique facial cleft | MONDO_0015415 | |
| Helicobacter pylori infection, susceptibility to | MONDO_0010853 | |
| chromosome 8Q12.1-q21.2 deletion syndrome | MONDO_0010852 | |
| complement receptor deficiency | MONDO_0022812 | |
| congenital absence of the sternocleidomastoid muscle | MONDO_0022815 | |
| congenital amputation | MONDO_0022817 | |
| congenital aneurysms of the great vessels | MONDO_0022818 | |
| Weismann-Netter syndrome | MONDO_0007209 | |
| Böök syndrome | MONDO_0007207 | |
| Boomerang dysplasia | MONDO_0007208 | |
| glycogen storage disease IXb | MONDO_0009868 |