All terms in MONDO
| Label | Id | Description |
|---|---|---|
| intellectual disability, autosomal recessive 27 | MONDO_0013702 | |
| corneal argyrosis | MONDO_0001716 | |
| basilar artery occlusion | MONDO_0001715 | |
| vertebral artery occlusion | MONDO_0001258 | |
| bejel | MONDO_0001714 | |
| gonococcal bursitis | MONDO_0001719 | |
| posterior corneal pigmentation | MONDO_0001717 | |
| progressive peripheral pterygium | MONDO_0001723 | |
| conjunctival pterygium | MONDO_0001055 | |
| central pterygium | MONDO_0001722 | |
| urethral intrinsic sphincter deficiency | MONDO_0001721 | |
| gonococcal synovitis | MONDO_0001720 | |
| surfactant metabolism dysfunction, pulmonary, 5 | MONDO_0013712 | |
| dengue virus, susceptibility to | MONDO_0013713 | |
| Lynch syndrome 5 | MONDO_0013710 | |
| peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome | MONDO_0013711 | |
| active cochleovestibular Meniere disease | MONDO_0001727 | |
| obsolete childhood disintegrative disease | MONDO_0001726 | |
| balanitis xerotica obliterans | MONDO_0001725 | |
| active cochlear Meniere disease | MONDO_0001729 |