| Label | Id | |
|---|---|---|
| spastic paraplegia 6, autosomal dominant | 10878 | |
| spastic paraplegia 6, autosomal dominant; SPG6 | http://purl.obolibrary.org/obo/MONDO_0010878 | |
| retinitis pigmentosa 63 | 13780 | |
| retinitis pigmentosa 63; RP63 | http://purl.obolibrary.org/obo/MONDO_0013780 | |
| retinitis pigmentosa 64 | 13786 | |
| optic atrophy 6; OPA6 | http://purl.obolibrary.org/obo/MONDO_0009786 | |
| partial trisomy 6q chromosome 6 | C537810 | |
| partial trisomy 6q syndrome | C537810 | |
| monosomy chromosome 7 | C537814 | |
| optic atrophy 7 | C567833 | |
| ring chromosome 7 syndrome | C537813 | |
| partial monosomy 7p chromosome 7 | C537818 | |
| Oral-facial-digital syndrome 8 | C557820 | |
| partial monosomy 8p2 chromosome 8 | C537826 | |
| orofacial cleft 9 | 12478 |