| Label | Id | |
|---|---|---|
| familial febrile, 2 convulsions | C566541 | |
| familial febrile, 2 seizures | C566541 | |
| cataract type 33 | 12665 | |
| cortical cataract 33 | http://purl.obolibrary.org/obo/MONDO_0012665 | |
| hemochromatosis, type 2b | C566557 | |
| familial combined, 1 hyperlipidemia | C566535 | |
| complementation group 1 peroxisome biogenesis disorder | C566568 | |
| autosomal recessive 18 deafness | C566580 | |
| limb-girdle, type 2g muscular dystrophy | C566599 | |
| familial hemiplegic, 3 migraine | C566500 | |
| parkinson disease 3, autosomal dominant lewy body | C566552 | |
| limb-girdle, type 1e muscular dystrophy | C566589 | |
| Mental Retardation, Autosomal Recessive 68 | 32665 | |
| ring chromosome 5 | 16654 | |
| rose cluster 5 | 16654 |