All terms in MONDO
| Label | Id | Description |
|---|---|---|
| familial temporal lobe epilepsy 7 | MONDO_0014639 | |
| temporal lobe epilepsy | MONDO_0005115 | |
| blepharochalasis | MONDO_0002660 | |
| Fanconi anemia complementation group T | MONDO_0014638 | |
| uveal disorder | MONDO_0002661 | |
| obsolete Bethlem myopathy 2 | MONDO_0014655 | |
| Ullrich congenital muscular dystrophy 2 | MONDO_0014654 | |
| retinitis pigmentosa 72 | MONDO_0014653 | |
| exudative vitreoretinopathy 6 | MONDO_0014652 | |
| exudative vitreoretinopathy | MONDO_0019516 | |
| infantile liver failure syndrome 2 | MONDO_0014659 | |
| infantile liver failure | MONDO_0000023 | |
| severe achondroplasia-developmental delay-acanthosis nigricans syndrome | MONDO_0014658 | |
| FGFR3-related chondrodysplasia | MONDO_0019685 | |
| primary ciliary dyskinesia 32 | MONDO_0014657 | |
| progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2 | MONDO_0014656 | |
| obsolete bare lymphocyte syndrome | MONDO_0000008 | |
| acrofacial dysostosis Cincinnati type | MONDO_0014651 | |
| familial temporal lobe epilepsy 8 | MONDO_0014650 | |
| colorblindness, partial | MONDO_0000014 |