| Db | Link | Name | Definition | Comment | Is a |
|---|---|---|---|---|---|
| OMIM | OMIM:118600 | CHONDROCALCINOSIS 2; CCAL2 | — | — | — |
| OMIM | OMIM:118610 | CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION | — | — | — |
| OMIM | OMIM:118650 | CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANT | — | — | — |
| OMIM | OMIM:118651 | CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE | — | — | — |
| OMIM | OMIM:118670 | CHONDRONECTIN | — | — | — |
| OMIM | OMIM:118700 | CHOREA, BENIGN HEREDITARY; BHC | — | — | — |
| OMIM | OMIM:118750 | CHOREOATHETOSIS, FAMILIAL INVERTED | — | — | — |
| OMIM | OMIM:118800 | PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1 | — | — | — |
| OMIM | OMIM:118830 | CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEIN LIPASE | — | — | — |
| OMIM | OMIM:118840 | CHROMATE RESISTANCE; CHR | — | — | — |
| OMIM | OMIM:118865 | CHOROIDAL OSTEOMA, BILATERAL | — | — | — |
| OMIM | OMIM:118900 | CIRRHOSIS, FAMILIAL | — | — | — |
| OMIM | OMIM:118940 | MOVED TO 118938 | — | — | — |
| OMIM | OMIM:118943 | CHYMOSIN PSEUDOGENE; CYMP | — | — | — |
| OMIM | OMIM:118953 | MOVED TO 192020 | — | — | — |
| OMIM | OMIM:118980 | CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL | — | — | — |
| OMIM | OMIM:119000 | CLEFT CHIN | — | — | — |
| OMIM | OMIM:119100 | SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1; SHFLD1 | — | — | — |
| OMIM | OMIM:119300 | VAN DER WOUDE SYNDROME 1; VWS1 | — | — | — |
| OMIM | OMIM:119500 | POPLITEAL PTERYGIUM SYNDROME; PPS | — | — | — |
| OMIM | OMIM:119530 | OROFACIAL CLEFT 1; OFC1 | — | — | — |
| OMIM | OMIM:119540 | CLEFT PALATE, ISOLATED; CPI | — | — | — |
| OMIM | OMIM:119550 | SYNGNATHIA | — | — | — |
| OMIM | OMIM:119570 | CLEFT SOFT PALATE | — | — | — |
| OMIM | OMIM:119580 | BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1 | — | — | — |