Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3	—	—	—
OMIM	OMIM:616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12	—	—	—
OMIM	OMIM:616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS	—	—	—
OMIM	OMIM:616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40	—	—	—
OMIM	OMIM:616580	AU-KLINE SYNDROME; AUKS	—	—	—
OMIM	OMIM:616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE; SEDSTN	—	—	—
OMIM	OMIM:616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B	—	—	—
OMIM	OMIM:616589	ADAMS-OLIVER SYNDROME 6; AOS6	—	—	—
OMIM	OMIM:616592	KOSAKI OVERGROWTH SYNDROME; KOGS	—	—	—
OMIM	OMIM:616602	CRANIOSYNOSTOSIS 6; CRS6	—	—	—
OMIM	OMIM:616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3	—	—	—
OMIM	OMIM:616604	CHROMOSOME 14q32 DUPLICATION SYNDROME, 700-KB	—	—	—
OMIM	OMIM:616606	RING CHROMOSOME 14 SYNDROME	—	—	—
OMIM	OMIM:616617	HEIMLER SYNDROME 2; HMLR2	—	—	—
OMIM	OMIM:616622	IMMUNODEFICIENCY 42; IMD42	—	—	—
OMIM	OMIM:616625	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W; CMT2W	—	—	—
OMIM	OMIM:616629	SENIOR-LOKEN SYNDROME 9; SLSN9	—	—	—
OMIM	OMIM:616631	POROKERATOSIS 9, MULTIPLE TYPES; POROK9	—	—	—
OMIM	OMIM:616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME; SCBMS	—	—	—
OMIM	OMIM:616636	IMMUNODEFICIENCY 44; IMD44	—	—	—
OMIM	OMIM:616638	SMITH-KINGSMORE SYNDROME; SKS	—	—	—
OMIM	OMIM:616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10; EPM10	—	—	—
OMIM	OMIM:616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34	—	—	—
OMIM	OMIM:616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35; EIEE35	—	—	—
OMIM	OMIM:616648	OPTIC ATROPHY 8; OPA8	—	—	—