| Db | Link | Name | Definition | Comment | Is a |
|---|---|---|---|---|---|
| OMIM | OMIM:132000 | EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS | — | — | — |
| OMIM | OMIM:132090 | EPILEPSY, BENIGN OCCIPITAL; BOE | — | — | — |
| OMIM | OMIM:132100 | PHOTOPAROXYSMAL RESPONSE 1; PPR1 | — | — | — |
| OMIM | OMIM:132300 | EPILEPSY, READING | — | — | — |
| OMIM | OMIM:132400 | EPIPHYSEAL DYSPLASIA, MULTIPLE, 1; EDM1 | — | — | — |
| OMIM | OMIM:132450 | EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS; EDMMD | — | — | — |
| OMIM | OMIM:132500 | EPISTAXIS, HEREDITARY | — | — | — |
| OMIM | OMIM:132600 | PILOMATRIXOMA | — | — | — |
| OMIM | OMIM:132700 | CYLINDROMATOSIS, FAMILIAL | — | — | — |
| OMIM | OMIM:132800 | MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO; MSSE | — | — | — |
| OMIM | OMIM:132850 | EPSTEIN-BARR VIRUS INSERTION SITE 1; EBVS1 | — | — | — |
| OMIM | OMIM:132860 | REMOVED FROM DATABASE | — | — | — |
| OMIM | OMIM:132900 | AORTIC ANEURYSM, FAMILIAL THORACIC 4; AAT4 | — | — | — |
| OMIM | OMIM:132990 | ERYTHEMA NODOSUM, FAMILIAL | — | — | — |
| OMIM | OMIM:133000 | ERYTHEMA PALMARE HEREDITARIUM | — | — | — |
| OMIM | OMIM:133020 | ERYTHERMALGIA, PRIMARY | — | — | — |
| OMIM | OMIM:133100 | ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1 | — | — | — |
| OMIM | OMIM:133180 | ERYTHROLEUKEMIA, FAMILIAL | — | — | — |
| OMIM | OMIM:133190 | SPINOCEREBELLAR ATAXIA 34; SCA34 | — | — | — |
| OMIM | OMIM:133200 | ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1; EKVP1 | — | — | — |
| OMIM | OMIM:133239 | ESOPHAGEAL CANCER | — | — | — |
| OMIM | OMIM:133240 | ESOPHAGEAL RING, LOWER | — | — | — |
| OMIM | OMIM:133250 | MOVED TO 172460 | — | — | — |
| OMIM | OMIM:133260 | ESTERASE B; ESB | — | — | — |
| OMIM | OMIM:133270 | ESTERASE C; ESC | — | — | — |