Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:119600	CLEIDOCRANIAL DYSPLASIA; CCD	—	—	—
OMIM	OMIM:119650	CLEIDORHIZOMELIC SYNDROME	—	—	—
OMIM	OMIM:119800	CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY; CCF	—	—	—
OMIM	OMIM:119900	DIGITAL CLUBBING, ISOLATED CONGENITAL	—	—	—
OMIM	OMIM:119915	CLUSTER HEADACHE, FAMILIAL	—	—	—
OMIM	OMIM:120000	COARCTATION OF AORTA	—	—	—
OMIM	OMIM:120040	COCHLEOSACCULAR DEGENERATION WITH PROGRESSIVE CATARACTS	—	—	—
OMIM	OMIM:120050	COXSACKIEVIRUS B3 SUSCEPTIBILITY; CXB3S	—	—	—
OMIM	OMIM:120080	COLCHICINE RESISTANCE	—	—	—
OMIM	OMIM:120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1; FCAS1	—	—	—
OMIM	OMIM:120140	COLLAGEN, TYPE II, ALPHA-1; COL2A1	—	—	—
OMIM	OMIM:120150	COLLAGEN, TYPE I, ALPHA-1; COL1A1	—	—	—
OMIM	OMIM:120200	COLOBOMA, OCULAR, AUTOSOMAL DOMINANT	—	—	—
OMIM	OMIM:120300	COLOBOMA OF MACULA	—	—	—
OMIM	OMIM:120310	MOVED TO 120140	—	—	—
OMIM	OMIM:120321	MOVED TO 120320	—	—	—
OMIM	OMIM:120327	MOVED TO 113811	—	—	—
OMIM	OMIM:120330	PAPILLORENAL SYNDROME; PAPRS	—	—	—
OMIM	OMIM:120400	COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY	—	—	—
OMIM	OMIM:120430	COLOBOMA OF OPTIC NERVE	—	—	—
OMIM	OMIM:120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1	—	—	—
OMIM	OMIM:120435	LYNCH SYNDROME I	—	—	—
OMIM	OMIM:120440	COLONIC VARICES WITHOUT PORTAL HYPERTENSION	—	—	—
OMIM	OMIM:120450	COMEDONES, FAMILIAL DYSKERATOTIC	—	—	—
OMIM	OMIM:120460	MOVED TO 191170	—	—	—