Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2	—	—	—
OMIM	OMIM:616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50	—	—	—
OMIM	OMIM:616459	AL-RAQAD SYNDROME; ARS	—	—	—
OMIM	OMIM:616460	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50; MRT50	—	—	—
OMIM	OMIM:616461	EPILEPSY, FAMILIAL TEMPORAL LOBE, 8; ETL8	—	—	—
OMIM	OMIM:616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN	—	—	—
OMIM	OMIM:616468	EXUDATIVE VITREORETINOPATHY 6; EVR6	—	—	—
OMIM	OMIM:616469	RETINITIS PIGMENTOSA 72; RP72	—	—	—
OMIM	OMIM:616470	ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2	—	—	—
OMIM	OMIM:616471	BETHLEM MYOPATHY 2; BTHLM2	—	—	—
OMIM	OMIM:616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2	—	—	—
OMIM	OMIM:616481	CILIARY DYSKINESIA, PRIMARY, 32; CILD32	—	—	—
OMIM	OMIM:616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN	—	—	—
OMIM	OMIM:616483	INFANTILE LIVER FAILURE SYNDROME 2; ILFS2	—	—	—
OMIM	OMIM:616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE; MCPH15	—	—	—
OMIM	OMIM:616487	EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY; EBSND	—	—	—
OMIM	OMIM:616488	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8	—	—	—
OMIM	OMIM:616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF	—	—	—
OMIM	OMIM:616490	JOUBERT SYNDROME 23; JBTS23	—	—	—
OMIM	OMIM:616491	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V	—	—	—
OMIM	OMIM:616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11	—	—	—
OMIM	OMIM:616500	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3; CEMCOX3	—	—	—
OMIM	OMIM:616501	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4; CEMCOX4	—	—	—
OMIM	OMIM:616502	CONE-ROD DYSTROPHY 21; CORD21	—	—	—
OMIM	OMIM:616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9	—	—	—