| Label | Id | |
|---|---|---|
| corneal type 1 macular dystrophy | C537834 | |
| congenital motor, 1 nystagmus | C537853 | |
| paroxysmal familial, 1 ventricular fibrillation | C567851 | |
| partial trisomy 10q | C537804 | |
| Tessier number 1-1 and 2-12 facial cleft | 15478 | |
| orofacial cleft 10 | 13378 | |
| orofacial cleft 10; OFC10 | http://purl.obolibrary.org/obo/MONDO_0013378 | |
| NOONAN SYNDROME 11 | 32786 | |
| Noonan syndrome 11 | 32786 | |
| Oral-facial-digital syndrome 11 | C557821 | |
| increased urinary 11-deoxytetrahydrocorticosterone level | C535978 | |
| distal deletion 11q | 7838 | |
| distal monosomy 11q | 7838 | |
| telomeric deletion 11q | 7838 | |
| parkinson disease 14, autosomal recessive | C567844 |