OMIM
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