Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:133300	ESTERASE ES-2, REGULATOR FOR	—	—	—
OMIM	OMIM:133420	MOVED TO 113710	—	—	—
OMIM	OMIM:133430	ESTROGEN RECEPTOR 1; ESR1	—	—	—
OMIM	OMIM:133500	EXCHONDROSIS OF PINNA, POSTERIOR	—	—	—
OMIM	OMIM:133540	COCKAYNE SYNDROME B; CSB	—	—	—
OMIM	OMIM:133600	EXOSTOSES OF HEEL	—	—	—
OMIM	OMIM:133690	EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E	—	—	—
OMIM	OMIM:133700	EXOSTOSES, MULTIPLE, TYPE I	—	—	—
OMIM	OMIM:133701	EXOSTOSES, MULTIPLE, TYPE II	—	—	—
OMIM	OMIM:133705	EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS	—	—	—
OMIM	OMIM:133710	REMOVED FROM DATABASE	—	—	—
OMIM	OMIM:133730	REMOVED FROM DATABASE	—	—	—
OMIM	OMIM:133740	REMOVED FROM DATABASE	—	—	—
OMIM	OMIM:133750	EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATION AND MICROCEPHALY	—	—	—
OMIM	OMIM:133780	EXUDATIVE VITREORETINOPATHY 1; EVR1	—	—	—
OMIM	OMIM:133800	EYEBROW, WHORL IN	—	—	—
OMIM	OMIM:133900	HEMIFACIAL HYPERPLASIA	—	—	—
OMIM	OMIM:134000	FACIAL HYPERTRICHOSIS	—	—	—
OMIM	OMIM:134100	MOVED TO 601471	—	—	—
OMIM	OMIM:134200	FACIAL PALSY, FAMILIAL RECURRENT PERIPHERAL	—	—	—
OMIM	OMIM:134300	FACIAL SPASM	—	—	—
OMIM	OMIM:134400	FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS	—	—	—
OMIM	OMIM:134430	FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF	—	—	—
OMIM	OMIM:134450	MOVED TO 613878	—	—	—
OMIM	OMIM:134500	FACTOR VIII DEFICIENCY	—	—	—