Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616949	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23	—	—	—
OMIM	OMIM:616950	SPERMATOGENIC FAILURE 15; SPGF15	—	—	—
OMIM	OMIM:616954	YOU-HOOVER-FONG SYNDROME; YHFS	—	—	—
OMIM	OMIM:616958	MOVED TO 608653	—	—	—
OMIM	OMIM:616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM	—	—	—
OMIM	OMIM:616963	HYPERCALCEMIA, INFANTILE, 2; HCINF2	—	—	—
OMIM	OMIM:616964	MOVED TO 615225	—	—	—
OMIM	OMIM:616968	DEAFNESS, AUTOSOMAL DOMINANT 70; DFNA70	—	—	—
OMIM	OMIM:616969	DEAFNESS, AUTOSOMAL DOMINANT 66; DFNA66	—	—	—
OMIM	OMIM:616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42; MRD42	—	—	—
OMIM	OMIM:616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30; COXPD30	—	—	—
OMIM	OMIM:616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART; NEDBEH	—	—	—
OMIM	OMIM:616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43	—	—	—
OMIM	OMIM:616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37	—	—	—
OMIM	OMIM:617004	POLYCYSTIC LIVER DISEASE 2 WITH OR WITHOUT KIDNEY CYSTS; PCLD2	—	—	—
OMIM	OMIM:617006	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2; ADMIO2	—	—	—
OMIM	OMIM:617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3; CPSQ3	—	—	—
OMIM	OMIM:617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR	—	—	—
OMIM	OMIM:617013	HYPERMANGANESEMIA WITH DYSTONIA 2; HMNDYT2	—	—	—
OMIM	OMIM:617014	NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE; SCN7	—	—	—
OMIM	OMIM:617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T	—	—	—
OMIM	OMIM:617018	SPINOCEREBELLAR ATAXIA 43; SCA43	—	—	—
OMIM	OMIM:617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38	—	—	—
OMIM	OMIM:617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA	—	—	—
OMIM	OMIM:617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10	—	—	—