All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Weill-Marchesani 4 syndrome, recessive | MONDO_0013176 | |
| congenital muscular dystrophy due to integrin alpha-7 deficiency | MONDO_0013177 | |
| primary ciliary dyskinesia 13 | MONDO_0013174 | |
| retinitis pigmentosa 50 | MONDO_0013175 | |
| MONDO_0025169 | MONDO_0025169 | |
| dislocation of ear ossicle | MONDO_0001199 | |
| obsolete rickettsialpox | MONDO_0001194 | |
| obsolete chorioretinal scar | MONDO_0001193 | |
| esophageal melanoma | MONDO_0001192 | |
| white heifer disease | MONDO_0025163 | |
| qualitative platelet defect | MONDO_0001197 | |
| reticuloendotheliosis, avian | MONDO_0025167 | |
| psychologic dyspareunia | MONDO_0001196 | |
| trichotillomania | MONDO_0013189 | |
| congenital stationary night blindness 1C | MONDO_0013183 | |
| congenital diarrhea 5 with tufting enteropathy | MONDO_0013184 | |
| amelogenesis imperfecta hypomaturation type 2A3 | MONDO_0013181 | |
| chromosome 17p13.3 duplication syndrome | MONDO_0013182 | |
| factor XIII, A subunit, deficiency of | MONDO_0013187 | |
| cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3 | MONDO_0013188 |