All terms in MONDO
| Label | Id | Description |
|---|---|---|
| endometriosis of intestine | MONDO_0001284 | |
| endosalpingiosis | MONDO_0001283 | |
| long QT syndrome 13 | MONDO_0013279 | |
| developmental and epileptic encephalopathy, 5 | MONDO_0013277 | |
| lymphatic malformation 3 | MONDO_0013278 | |
| frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome | MONDO_0013271 | |
| chromosome 14q11-q22 deletion syndrome | MONDO_0013272 | |
| Rett syndrome, congenital variant | MONDO_0013270 | |
| hemolytic anemia due to glucophosphate isomerase deficiency | MONDO_0013275 | |
| Reynolds syndrome | MONDO_0013276 | |
| chromosome 16p13.3 duplication syndrome | MONDO_0013273 | |
| retinitis pigmentosa 51 | MONDO_0013274 | |
| diabetic autonomic neuropathy | MONDO_0001299 | |
| congenital mitral valve insufficiency | MONDO_0001298 | |
| brain compression | MONDO_0001291 | |
| allergic cutaneous vasculitis | MONDO_0001290 | |
| cardiac tamponade | MONDO_0001297 | |
| acquired night blindness | MONDO_0001296 | |
| strongyle infections, equine | MONDO_0025263 | |
| idiopathic peripheral autonomic neuropathy | MONDO_0001295 |