Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS	—	—	—
OMIM	OMIM:617622	JOUBERT SYNDROME 30; JBTS30	—	—	—
OMIM	OMIM:617626	FIBROMATOSIS, GINGIVAL, 5; GINGF5	—	—	—
OMIM	OMIM:617629	SCHIZOPHRENIA 19; SCZD19	—	—	—
OMIM	OMIM:617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26	—	—	—
OMIM	OMIM:617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47	—	—	—
OMIM	OMIM:617637	DEAFNESS, AUTOSOMAL RECESSIVE 106; DFNB106	—	—	—
OMIM	OMIM:617638	IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS; IMD11B	—	—	—
OMIM	OMIM:617639	DEAFNESS, AUTOSOMAL RECESSIVE 107; DFNB107	—	—	—
OMIM	OMIM:617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED	—	—	—
OMIM	OMIM:617642	POLYDACTYLY, POSTAXIAL, TYPE A7; PAPA7	—	—	—
OMIM	OMIM:617643	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS	—	—	—
OMIM	OMIM:617644	SPERMATOGENIC FAILURE 21; SPGF21	—	—	—
OMIM	OMIM:617654	DEAFNESS, AUTOSOMAL RECESSIVE 108; DFNB108	—	—	—
OMIM	OMIM:617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1	—	—	—
OMIM	OMIM:617661	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2; VCRL2	—	—	—
OMIM	OMIM:617662	JOINT LAXITY, SHORT STATURE, AND MYOPIA; JLSM	—	—	—
OMIM	OMIM:617663	DEAFNESS, AUTOSOMAL DOMINANT 73; DFNA73	—	—	—
OMIM	OMIM:617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32	—	—	—
OMIM	OMIM:617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56	—	—	—
OMIM	OMIM:617666	FRASER SYNDROME 2; FRASRS2	—	—	—
OMIM	OMIM:617667	FRASER SYNDROME 3; FRASRS3	—	—	—
OMIM	OMIM:617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA	—	—	—
OMIM	OMIM:617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS	—	—	—
OMIM	OMIM:617671	HELIX SYNDROME; HELIX	—	—	—