All terms in MONDO
| Label | Id | Description |
|---|---|---|
| PEHO-like syndrome | MONDO_0020495 | |
| oculootodental syndrome | MONDO_0020494 | |
| Haddad syndrome | MONDO_0020493 | |
| pituitary gigantism | MONDO_0020479 | |
| myotonia fluctuans | MONDO_0020481 | |
| Pontiac fever | MONDO_0020487 | |
| legionellosis | MONDO_0005823 | |
| MONDO_0020486 | MONDO_0020486 | |
| King-Denborough syndrome | MONDO_0020485 | |
| obsolete rare familial disorder with hypertrophic cardiomyopathy | MONDO_0020484 | |
| acetazolamide-responsive myotonia | MONDO_0020483 | |
| myotonia permanens | MONDO_0020482 | |
| central core myopathy | MONDO_0007294 | |
| childhood epilepsy with centrotemporal spikes | MONDO_0007295 | |
| obsolete celiac artery stenosis from compression by median arcuate ligament of diaphragm | MONDO_0007292 | |
| leukocyte adhesion deficiency 1 | MONDO_0007293 | |
| leukocyte adhesion deficiency | MONDO_0017570 | |
| cataract 5 multiple types | MONDO_0007290 | |
| obsolete familial cerebral cavernous malformation | MONDO_0007291 | |
| obsolete median-ulnar nerve communications | MONDO_0044239 |