Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:102000	ACROLEUKOPATHY, SYMMETRIC	—	—	—
OMIM	OMIM:102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA	—	—	—
OMIM	OMIM:102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME	—	—	—
OMIM	OMIM:102200	PITUITARY ADENOMA 1, MULTIPLE TYPES; PITA1	—	—	—
OMIM	OMIM:102300	RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1	—	—	—
OMIM	OMIM:102350	ACROMIAL DIMPLES	—	—	—
OMIM	OMIM:102370	ACROMICRIC DYSPLASIA; ACMICD	—	—	—
OMIM	OMIM:102400	ACROOSTEOLYSIS	—	—	—
OMIM	OMIM:102490	MOVED TO 607323	—	—	—
OMIM	OMIM:102500	HAJDU-CHENEY SYNDROME; HJCYS	—	—	—
OMIM	OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA; ACRPV	—	—	—
OMIM	OMIM:102520	ACRORENAL SYNDROME	—	—	—
OMIM	OMIM:102530	SPERMATOGENIC FAILURE 6; SPGF6	—	—	—
OMIM	OMIM:102550	MOVED TO 102630	—	—	—
OMIM	OMIM:102570	REMOVED FROM DATABASE	—	—	—
OMIM	OMIM:102590	ACYLASE, COBALT-ACTIVATED	—	—	—
OMIM	OMIM:102640	MOVED TO 102630	—	—	—
OMIM	OMIM:102650	ADACTYLIA, UNILATERAL	—	—	—
OMIM	OMIM:102660	ADAMANTINOMA OF LONG BONES	—	—	—
OMIM	OMIM:102699	ADENO-ASSOCIATED VIRUS INTEGRATION SITE 1; AAVS1	—	—	—
OMIM	OMIM:102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY	—	—	—
OMIM	OMIM:102710	MOVED TO 102720	—	—	—
OMIM	OMIM:102730	ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO	—	—	—
OMIM	OMIM:102800	ADENOSINE TRIPHOSPHATASE DEFICIENCY, ANEMIA DUE TO	—	—	—
OMIM	OMIM:102900	ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES	—	—	—