| Db | Link | Name | Definition | Comment | Is a |
|---|---|---|---|---|---|
| OMIM | OMIM:102920 | REMOVED FROM DATABASE | — | — | — |
| OMIM | OMIM:102930 | REMOVED FROM DATABASE | — | — | — |
| OMIM | OMIM:102940 | REMOVED FROM DATABASE | — | — | — |
| OMIM | OMIM:102970 | REMOVED FROM DATABASE | — | — | — |
| OMIM | OMIM:102990 | MOVED TO 145600 | — | — | — |
| OMIM | OMIM:103050 | ADENYLOSUCCINASE DEFICIENCY; ADSLD | — | — | — |
| OMIM | OMIM:103100 | ADIE PUPIL | — | — | — |
| OMIM | OMIM:103200 | ADIPOSIS DOLOROSA | — | — | — |
| OMIM | OMIM:103230 | ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL | — | — | — |
| OMIM | OMIM:103285 | ADULT SYNDROME | — | — | — |
| OMIM | OMIM:103300 | HYPOGLOSSIA-HYPODACTYLIA | — | — | — |
| OMIM | OMIM:103321 | MOVED TO 128239 | — | — | — |
| OMIM | OMIM:103400 | AINHUM | — | — | — |
| OMIM | OMIM:103420 | ALACRIMA, CONGENITAL, AUTOSOMAL DOMINANT | — | — | — |
| OMIM | OMIM:103470 | ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS | — | — | — |
| OMIM | OMIM:103500 | TIETZ ALBINISM-DEAFNESS SYNDROME; TADS | — | — | — |
| OMIM | OMIM:103580 | PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A | — | — | — |
| OMIM | OMIM:103581 | MOVED TO 103580 | — | — | — |
| OMIM | OMIM:103780 | ALCOHOL DEPENDENCE | — | — | — |
| OMIM | OMIM:103800 | MOVED TO 253200 AND 258870 | — | — | — |
| OMIM | OMIM:103900 | HYPERALDOSTERONISM, FAMILIAL, TYPE I; HALD1 | — | — | — |
| OMIM | OMIM:103920 | ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS, FAMILIAL | — | — | — |
| OMIM | OMIM:104000 | ALOPECIA AREATA 1; AA1 | — | — | — |
| OMIM | OMIM:104100 | PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1 | — | — | — |
| OMIM | OMIM:104110 | ALOPECIA, FAMILIAL FOCAL; ALPF | — | — | — |