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 |
— |
— |
— |