Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:114620	CRANIOFACIOFRONTODIGITAL SYNDROME	—	—	—
OMIM	OMIM:114650	CAR FACTOR DEFICIENCY	—	—	—
OMIM	OMIM:114700	CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH	—	—	—
OMIM	OMIM:114836	MOVED TO 114835	—	—	—
OMIM	OMIM:114841	MOVED TO 114840	—	—	—
OMIM	OMIM:114900	CARCINOID TUMORS, INTESTINAL	—	—	—
OMIM	OMIM:115000	CARDIAC ARRHYTHMIA	—	—	—
OMIM	OMIM:115080	CARDIAC CONDUCTION DEFECT	—	—	—
OMIM	OMIM:115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1	—	—	—
OMIM	OMIM:115195	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2	—	—	—
OMIM	OMIM:115196	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3	—	—	—
OMIM	OMIM:115197	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4	—	—	—
OMIM	OMIM:115198	MOVED TO 192600 AND 115197	—	—	—
OMIM	OMIM:115200	CARDIOMYOPATHY, DILATED, 1A; CMD1A	—	—	—
OMIM	OMIM:115210	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1; RCM1	—	—	—
OMIM	OMIM:115250	COLLAGENOMA, FAMILIAL CUTANEOUS	—	—	—
OMIM	OMIM:115300	HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL DOMINANT; HCVAD	—	—	—
OMIM	OMIM:115310	PARAGANGLIOMAS 4; PGL4	—	—	—
OMIM	OMIM:115400	CARPAL DISPLACEMENT	—	—	—
OMIM	OMIM:115430	CARPAL TUNNEL SYNDROME; CTS1	—	—	—
OMIM	OMIM:115470	CAT EYE SYNDROME; CES	—	—	—
OMIM	OMIM:115645	CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION	—	—	—
OMIM	OMIM:115650	CATARACT 32, MULTIPLE TYPES; CTRCT32	—	—	—
OMIM	OMIM:115660	CATARACT 7; CTRCT7	—	—	—
OMIM	OMIM:115665	CATARACT 8, MULTIPLE TYPES; CTRCT8	—	—	—