Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B	—	—	—
OMIM	OMIM:616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17	—	—	—
OMIM	OMIM:616509	CATARACT 44; CTRCT44	—	—	—
OMIM	OMIM:616511	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14; MODY14	—	—	—
OMIM	OMIM:616515	DEAFNESS, AUTOSOMAL RECESSIVE 104; DFNB104	—	—	—
OMIM	OMIM:616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3	—	—	—
OMIM	OMIM:616517	ACHROMATOPSIA 7; ACHM7	—	—	—
OMIM	OMIM:616521	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39; MRD39	—	—	—
OMIM	OMIM:616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA	—	—	—
OMIM	OMIM:616532	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 7; IIAE7	—	—	—
OMIM	OMIM:616534	THYROID CANCER, NONMEDULLARY, 4; NMTC4	—	—	—
OMIM	OMIM:616535	THYROID CANCER, NONMEDULLARY, 5; NMTC5	—	—	—
OMIM	OMIM:616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9	—	—	—
OMIM	OMIM:616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26	—	—	—
OMIM	OMIM:616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9	—	—	—
OMIM	OMIM:616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED	—	—	—
OMIM	OMIM:616544	RETINITIS PIGMENTOSA 73; RP73	—	—	—
OMIM	OMIM:616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY; SRTD14	—	—	—
OMIM	OMIM:616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4	—	—	—
OMIM	OMIM:616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6	—	—	—
OMIM	OMIM:616559	NOONAN SYNDROME 9; NS9	—	—	—
OMIM	OMIM:616562	RETINITIS PIGMENTOSA 74; RP74	—	—	—
OMIM	OMIM:616564	NOONAN SYNDROME 10; NS10	—	—	—
OMIM	OMIM:616566	SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE; SCDO6	—	—	—
OMIM	OMIM:616568	GLIOMA SUSCEPTIBILITY 9; GLM9	—	—	—