OMIM
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