All terms in MONDO
| Label | Id | Description |
|---|---|---|
| gallbladder disease 3 | MONDO_0012366 | |
| hereditary gallbladder disorder | MONDO_0700225 | |
| retinitis pigmentosa 31 | MONDO_0012367 | |
| dilated cardiomyopathy 1Q | MONDO_0012364 | |
| gallbladder disease 2 | MONDO_0012365 | |
| aminoacylase 1 deficiency | MONDO_0012368 | |
| inborn aminoacylase deficiency | MONDO_0017686 | |
| systemic lupus erythematosus, susceptibility to, 6 | MONDO_0012369 | |
| dilated cardiomyopathy 1P | MONDO_0012362 | |
| retinitis pigmentosa 32 | MONDO_0012363 | |
| congenital nongoitrous hypothryoidism 3 | MONDO_0012360 | |
| hypothyroidism, congenital, nongoitrous | MONDO_0000045 | |
| peripheral resistance to thyroid hormones | MONDO_0019995 | |
| systemic lupus erythematosus, susceptibility to, 5 | MONDO_0012361 | |
| obsolete anonychia congenita | MONDO_0000388 | |
| hypochromic microcytic anemia | MONDO_0000387 | |
| hypochromic anemia | MONDO_0001357 | |
| drug induced central sleep apnea | MONDO_0024357 | |
| primary central sleep apnea syndrome | MONDO_0024356 | |
| central sleep apnea due to periodic breathing | MONDO_0024359 |