All terms in MONDO
| Label | Id | Description |
|---|---|---|
| plasma fibronectin deficiency | MONDO_0013575 | |
| methylmalonate semialdehyde dehydrogenase deficiency | MONDO_0013579 | |
| Keppen-Lubinsky syndrome | MONDO_0013572 | |
| cranioectodermal dysplasia 3 | MONDO_0013573 | |
| combined oxidative phosphorylation defect type 8 | MONDO_0013570 | |
| acatalasia | MONDO_0013571 | |
| benign lymphoepithelial lesion of salivary gland | MONDO_0001598 | |
| hypochondriasis | MONDO_0001596 | |
| obsolete Mikulicz disease | MONDO_0001599 | |
| quadriplegia | MONDO_0001590 | |
| Achilles bursitis | MONDO_0001594 | |
| skeletal ligament disorder | MONDO_0045004 | |
| senile entropion | MONDO_0001591 | |
| glycogen storage disease due to lactate dehydrogenase H-subunit deficiency | MONDO_0013587 | |
| Perrault syndrome 3 | MONDO_0013588 | |
| hydrolethalus syndrome 2 | MONDO_0013585 | |
| obsolete Chitotriosidase deficiency | MONDO_0013586 | |
| focal segmental glomerulosclerosis 6 | MONDO_0013589 | |
| pyruvate dehydrogenase E1-beta deficiency | MONDO_0013580 | |
| occipital pachygyria and polymicrogyria | MONDO_0013583 |