Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616784	JOUBERT SYNDROME 26; JBTS26	—	—	—
OMIM	OMIM:616788	OROFACIAL CLEFT 15; OFC15	—	—	—
OMIM	OMIM:616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD	—	—	—
OMIM	OMIM:616792	NEUROBLASTOMA, SUSCEPTIBILITY TO, 7; NBLST7	—	—	—
OMIM	OMIM:616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28; COXPD28	—	—	—
OMIM	OMIM:616795	SPINOCEREBELLAR ATAXIA 42; SCA42	—	—	—
OMIM	OMIM:616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2	—	—	—
OMIM	OMIM:616803	LAMB-SHAFFER SYNDROME; LAMSHF	—	—	—
OMIM	OMIM:616806	WILMS TUMOR 6; WT6	—	—	—
OMIM	OMIM:616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6; HPMRS6	—	—	—
OMIM	OMIM:616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29; COXPD29	—	—	—
OMIM	OMIM:616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X	—	—	—
OMIM	OMIM:616814	PREIMPLANTATION EMBRYONIC LETHALITY 1; PREMBL1	—	—	—
OMIM	OMIM:616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR	—	—	—
OMIM	OMIM:616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2; MSSGM2	—	—	—
OMIM	OMIM:616818	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 3; IGAN3	—	—	—
OMIM	OMIM:616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA	—	—	—
OMIM	OMIM:616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W	—	—	—
OMIM	OMIM:616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIo; CDG2O	—	—	—
OMIM	OMIM:616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp; CDG2P	—	—	—
OMIM	OMIM:616831	LUSCAN-LUMISH SYNDROME; LLS	—	—	—
OMIM	OMIM:616833	PAGET DISEASE OF BONE 6; PDB6	—	—	—
OMIM	OMIM:616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS; MCCPD	—	—	—
OMIM	OMIM:616835	MEIER-GORLIN SYNDROME 6; MGORS6	—	—	—
OMIM	OMIM:616839	EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE; RREI	—	—	—