Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616233	MOVED TO 614881	—	—	—
OMIM	OMIM:616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24	—	—	—
OMIM	OMIM:616247	LONG QT SYNDROME 14; LQT14	—	—	—
OMIM	OMIM:616248	LETHAL CONGENITAL CONTRACTURE SYNDROME 6; LCCS6	—	—	—
OMIM	OMIM:616249	LONG QT SYNDROME 15; LQT15	—	—	—
OMIM	OMIM:616255	SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES; SNSK	—	—	—
OMIM	OMIM:616258	MECKEL SYNDROME 12; MKS12	—	—	—
OMIM	OMIM:616260	TENORIO SYNDROME; TNORS	—	—	—
OMIM	OMIM:616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET; IMNEPD	—	—	—
OMIM	OMIM:616265	PEELING SKIN SYNDROME 3; PSS3	—	—	—
OMIM	OMIM:616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY; CLIFAHDD	—	—	—
OMIM	OMIM:616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4	—	—	—
OMIM	OMIM:616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32	—	—	—
OMIM	OMIM:616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48	—	—	—
OMIM	OMIM:616270	AMELOGENESIS IMPERFECTA, TYPE IF; AI1F	—	—	—
OMIM	OMIM:616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN	—	—	—
OMIM	OMIM:616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7	—	—	—
OMIM	OMIM:616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D	—	—	—
OMIM	OMIM:616278	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5	—	—	—
OMIM	OMIM:616279	CATARACT 43; CTRCT43	—	—	—
OMIM	OMIM:616280	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U; CMT2U	—	—	—
OMIM	OMIM:616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49	—	—	—
OMIM	OMIM:616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73	—	—	—
OMIM	OMIM:616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7	—	—	—
OMIM	OMIM:616287	LETHAL CONGENITAL CONTRACTURE SYNDROME 8; LCCS8	—	—	—