All terms in MONDO
| Label | Id | Description |
|---|---|---|
| obsolete rare genetic systemic or rheumatologic disease | MONDO_0028795 | |
| obsolete fallopian tube carcinosarcoma | MONDO_0002161 | |
| fallopian tube adenosarcoma | MONDO_0002162 | |
| adenosarcoma | MONDO_0005636 | |
| autosomal recessive spinocerebellar ataxia 14 | MONDO_0014159 | |
| nephronophthisis 16 | MONDO_0014158 | |
| nephronophthisis | MONDO_0019005 | |
| mandibular hypoplasia-deafness-progeroid syndrome | MONDO_0014157 | |
| intraoperative floppy iris syndrome | MONDO_0041775 | |
| iris disorder | MONDO_0002289 | |
| left ventricular noncompaction 8 | MONDO_0014152 | |
| familial isolated dilated cardiomyopathy | MONDO_0015470 | |
| pulmonary hypertension, neonatal, susceptibility to | MONDO_0014151 | |
| pulmonary hypertension, neonatal | MONDO_0100159 | |
| developmental and epileptic encephalopathy 94 | MONDO_0014150 | |
| myoclonic-astastic epilepsy | MONDO_0016025 | |
| Lennox-Gastaut syndrome | MONDO_0016532 | |
| atrial fibrillation, familial, 14 | MONDO_0014156 | |
| atrial fibrillation, familial, 13 | MONDO_0014155 | |
| Charcot-Marie-Tooth disease recessive intermediate C | MONDO_0014154 |