All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1 | MONDO_0025622 | |
| acute cystitis | MONDO_0001650 | |
| megaesophagus | MONDO_0001656 | |
| dissociated nystagmus | MONDO_0001655 | |
| spermatic cord cancer | MONDO_0001654 | |
| hyperphosphatasia with intellectual disability syndrome 3 | MONDO_0013628 | |
| intellectual disability, autosomal recessive 16 | MONDO_0013629 | |
| psoriasis 14, pustular | MONDO_0013626 | |
| 3M syndrome 3 | MONDO_0013627 | |
| holoprosencephaly 11 | MONDO_0013642 | |
| hyperuricemic nephropathy, familial juvenile type 3 | MONDO_0013643 | |
| familial retinal arterial macroaneurysm | MONDO_0013640 | |
| Warburg micro syndrome 2 | MONDO_0013641 | |
| chromosome 8q21.11 deletion syndrome | MONDO_0013646 | |
| obsolete primary microcephaly-epilepsy-permanent neonatal diabetes syndrome | MONDO_0013647 | |
| Charcot-Marie-Tooth disease axonal type 2O | MONDO_0013644 | |
| autosomal recessive spinocerebellar ataxia 11 | MONDO_0013645 | |
| obsolete MONDO:0001659 | MONDO_0001659 | |
| nontoxic goiter | MONDO_0001658 | |
| submucous uterine fibroid | MONDO_0001664 |