OMIM
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 — — —