Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:122100	CORNEAL DYSTROPHY, MEESMANN; MECD	—	—	—
OMIM	OMIM:122200	CORNEAL DYSTROPHY, LATTICE TYPE I; LCD1	—	—	—
OMIM	OMIM:122400	EPITHELIAL RECURRENT EROSION DYSTROPHY; ERED	—	—	—
OMIM	OMIM:122430	CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS, UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION	—	—	—
OMIM	OMIM:122440	CORNEODERMATOOSSEOUS SYNDROME	—	—	—
OMIM	OMIM:122450	CORNEAL HYPESTHESIA, FAMILIAL	—	—	—
OMIM	OMIM:122455	CORONARY ARTERY DISSECTION, SPONTANEOUS	—	—	—
OMIM	OMIM:122460	HUMAN CORONAVIRUS SENSITIVITY; HCVS	—	—	—
OMIM	OMIM:122470	CORNELIA DE LANGE SYNDROME 1; CDLS1	—	—	—
OMIM	OMIM:122480	MOVED TO 166740	—	—	—
OMIM	OMIM:122550	CORTICOSTERONE SIDE-CHAIN ISOMERASE; CSCI	—	—	—
OMIM	OMIM:122580	COSTOCORACOID LIGAMENT, CONGENITALLY SHORT	—	—	—
OMIM	OMIM:122600	SPONDYLOCOSTAL DYSOSTOSIS 5; SCDO5	—	—	—
OMIM	OMIM:122700	COUMARIN RESISTANCE	—	—	—
OMIM	OMIM:122720	CYTOCHROME P450, SUBFAMILY IIA, POLYPEPTIDE 6; CYP2A6	—	—	—
OMIM	OMIM:122750	COXA VARA	—	—	—
OMIM	OMIM:122780	COXOAURICULAR SYNDROME	—	—	—
OMIM	OMIM:122850	CRANIOACROFACIAL SYNDROME	—	—	—
OMIM	OMIM:122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD	—	—	—
OMIM	OMIM:122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS	—	—	—
OMIM	OMIM:122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA	—	—	—
OMIM	OMIM:122920	MOVED TO 304110	—	—	—
OMIM	OMIM:123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CMDD	—	—	—
OMIM	OMIM:123050	CRANIORHINY	—	—	—
OMIM	OMIM:123100	CRANIOSYNOSTOSIS 1; CRS1	—	—	—