All terms in MONDO
| Label | Id | Description |
|---|---|---|
| obsolete Simpson-Golabi-Behmel syndrome | MONDO_0000725 | |
| obsolete congenital ptosis | MONDO_0000729 | |
| obsolete peeling skin syndrome | MONDO_0000731 | |
| obsolete pontocerebellar hypoplasia | MONDO_0000730 | |
| dilated cardiomyopathy 1X | MONDO_0012704 | |
| familial temporal lobe epilepsy 3 | MONDO_0012705 | |
| celiac disease, susceptibility to, 6 | MONDO_0012702 | |
| lissencephaly due to TUBA1A mutation | MONDO_0012703 | |
| primary lateral sclerosis, adult, 1 | MONDO_0012708 | |
| microphthalmia, isolated, with coloboma 5 | MONDO_0012709 | |
| familial temporal lobe epilepsy 4 | MONDO_0012706 | |
| familial febrile seizures 9 | MONDO_0012707 | |
| Dauwerse-Peters syndrome | MONDO_0012722 | |
| Leber congenital amaurosis 10 | MONDO_0012723 | |
| Krabbe disease due to saposin A deficiency | MONDO_0012720 | |
| progressive myoclonic epilepsy type 3 | MONDO_0012721 | |
| obsolete megalocornea | MONDO_0000737 | |
| obsolete oculodentodigital dysplasia | MONDO_0000735 | |
| blepharophimosis - intellectual disability syndrome | MONDO_0017393 | |
| uvulitis | MONDO_0000739 |