Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:108340	ARYL HYDROCARBON HYDROXYLASE INDUCIBILITY	—	—	—
OMIM	OMIM:108390	ASPARAGUS, SPECIFIC SMELL HYPERSENSITIVITY	—	—	—
OMIM	OMIM:108400	REMOVED FROM DATABASE	—	—	—
OMIM	OMIM:108420	SPERMATOGENIC FAILURE 2; SPGF2	—	—	—
OMIM	OMIM:108450	ASYMMETRIC SHORT STATURE SYNDROME	—	—	—
OMIM	OMIM:108500	EPISODIC ATAXIA, TYPE 2; EA2	—	—	—
OMIM	OMIM:108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1	—	—	—
OMIM	OMIM:108650	SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7	—	—	—
OMIM	OMIM:108700	ATAXIA WITH FASCICULATIONS	—	—	—
OMIM	OMIM:108720	ATELOSTEOGENESIS, TYPE I; AO1	—	—	—
OMIM	OMIM:108721	ATELOSTEOGENESIS, TYPE III; AO3	—	—	—
OMIM	OMIM:108725	ATHEROSCLEROSIS SUSCEPTIBILITY; ATHS	—	—	—
OMIM	OMIM:108760	ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTIVE DEAFNESS	—	—	—
OMIM	OMIM:108770	ATRIAL STANDSTILL 1; ATRST1	—	—	—
OMIM	OMIM:108800	ATRIAL SEPTAL DEFECT 1; ASD1	—	—	—
OMIM	OMIM:108900	ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS; ASD7	—	—	—
OMIM	OMIM:108950	ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL	—	—	—
OMIM	OMIM:108970	MOVED TO 120520	—	—	—
OMIM	OMIM:108980	PR INTERVAL, VARIATION IN	—	—	—
OMIM	OMIM:108985	SVEINSSON CHORIORETINAL ATROPHY; SCRA	—	—	—
OMIM	OMIM:109000	AURICULOOSTEODYSPLASIA	—	—	—
OMIM	OMIM:109050	AUROCEPHALOSYNDACTYLY	—	—	—
OMIM	OMIM:109100	AUTOIMMUNE DISEASE	—	—	—
OMIM	OMIM:109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES	—	—	—
OMIM	OMIM:109130	AXIAL OSTEOMALACIA	—	—	—