All terms in MONDO
| Label | Id | Description |
|---|---|---|
| immunotactoid or fibrillary glomerulopathy | MONDO_0019605 | |
| acquired monoclonal Ig light chain-associated Fanconi syndrome | MONDO_0019604 | |
| obsolete autosomal recessive axonal hereditary motor and sensory neuropathy | MONDO_0019601 | |
| fragile site 10Q23 | MONDO_0007629 | |
| focal facial dermal dysplasia type I | MONDO_0007627 | |
| foveal hypoplasia 1 | MONDO_0007628 | |
| focal epithelial hyperplasia of the oral mucosa | MONDO_0007625 | |
| familial congenital palsy of trochlear nerve | MONDO_0007626 | |
| fourth cranial nerve palsy | MONDO_0001146 | |
| congenital trochlear nerve palsy | MONDO_0020256 | |
| flushing of ears and somnolence | MONDO_0007623 | |
| Flynn-Aird syndrome | MONDO_0007624 | |
| Floating-Harbor syndrome | MONDO_0007621 | |
| obsolete flood factor deficiency | MONDO_0007622 | |
| fish eye disease | MONDO_0007620 | |
| Sheehan syndrome | MONDO_0019618 | |
| Liddle syndrome 1 | MONDO_0020607 | |
| pituitary deficiency due to empty sella turcica syndrome | MONDO_0019617 | |
| sex-linked disease | MONDO_0020606 | |
| duplication of the esophagus | MONDO_0019619 |