Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:120500	COMMISSURAL LIP PITS	—	—	—
OMIM	OMIM:120502	BRANCHIOOTIC SYNDROME 2	—	—	—
OMIM	OMIM:120790	COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF	—	—	—
OMIM	OMIM:120832	MOVED TO 120830	—	—	—
OMIM	OMIM:120970	CONE-ROD DYSTROPHY 2; CORD2	—	—	—
OMIM	OMIM:121000	REMOVED FROM DATABASE	—	—	—
OMIM	OMIM:121020	MOVED TO 160120	—	—	—
OMIM	OMIM:121050	ARTHROGRYPOSIS, DISTAL, TYPE 9; DA9	—	—	—
OMIM	OMIM:121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E	—	—	—
OMIM	OMIM:121200	SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1	—	—	—
OMIM	OMIM:121201	SEIZURES, BENIGN FAMILIAL NEONATAL, 2; BFNS2	—	—	—
OMIM	OMIM:121210	FEBRILE SEIZURES, FAMILIAL, 1; FEB1	—	—	—
OMIM	OMIM:121250	MOVED TO 300088	—	—	—
OMIM	OMIM:121270	COPPER DEFICIENCY, FAMILIAL BENIGN	—	—	—
OMIM	OMIM:121300	COPROPORPHYRIA, HEREDITARY; HCP	—	—	—
OMIM	OMIM:121350	CORACOCLAVICULAR JOINT, ANOMALOUS	—	—	—
OMIM	OMIM:121390	CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS	—	—	—
OMIM	OMIM:121400	CORNEA PLANA 1, AUTOSOMAL DOMINANT; CNA1	—	—	—
OMIM	OMIM:121450	CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS	—	—	—
OMIM	OMIM:121700	MOVED TO 122000	—	—	—
OMIM	OMIM:121800	SCHNYDER CORNEAL DYSTROPHY; SCCD	—	—	—
OMIM	OMIM:121820	CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE; EBMD	—	—	—
OMIM	OMIM:121850	CORNEAL DYSTROPHY, FLECK	—	—	—
OMIM	OMIM:121900	CORNEAL DYSTROPHY, GROENOUW TYPE I; CDGG1	—	—	—
OMIM	OMIM:122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1; PPCD1	—	—	—