All terms in MONDO
| Label | Id | Description |
|---|---|---|
| specific language impairment 4 | MONDO_0012917 | |
| primary ciliary dyskinesia 10 | MONDO_0012918 | |
| chromosome 1q21.1 duplication syndrome | MONDO_0012915 | |
| chromosome 2p16.1-p15 deletion syndrome | MONDO_0012916 | |
| focal segmental glomerulosclerosis 4, susceptibility to | MONDO_0012931 | |
| myopia 16, autosomal dominant | MONDO_0012932 | |
| autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | MONDO_0012930 | |
| psychologic vaginismus | MONDO_0000946 | |
| psychosexual disorder | MONDO_0000947 | |
| venous insufficiency | MONDO_0000945 | |
| cerebral artery occlusion | MONDO_0000944 | |
| arterial occlusion | MONDO_0020673 | |
| acute hydrops keratoconus | MONDO_0000943 | |
| conjunctival degeneration | MONDO_0000949 | |
| xerophthalmia | MONDO_0000948 | |
| sexual and gender identity disorders | MONDO_0000595 | |
| cancer of short bone of lower limb | MONDO_0000953 | |
| thymus lymphoma | MONDO_0000951 | |
| asthenopia | MONDO_0000950 | |
| Diamond-Blackfan anemia 4 | MONDO_0012924 |