Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58	—	—	—
OMIM	OMIM:617271	NEPHRONOPHTHISIS 20; NPHP20	—	—	—
OMIM	OMIM:617272	GLAUCOMA 3, PRIMARY CONGENITAL, E; GLC3E	—	—	—
OMIM	OMIM:617275	TOOTH AGENESIS, SELECTIVE, 9; STHAG9	—	—	—
OMIM	OMIM:617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48; EIEE48	—	—	—
OMIM	OMIM:617280	ATRIAL FIBRILLATION, FAMILIAL, 18; ATFB18	—	—	—
OMIM	OMIM:617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49	—	—	—
OMIM	OMIM:617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG	—	—	—
OMIM	OMIM:617284	DYSTONIA 28, CHILDHOOD-ONSET; DYT28	—	—	—
OMIM	OMIM:617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D	—	—	—
OMIM	OMIM:617294	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS; EBSSH	—	—	—
OMIM	OMIM:617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY; SINO	—	—	—
OMIM	OMIM:617297	AMELOGENESIS IMPERFECTA, TYPE IJ; AI1J	—	—	—
OMIM	OMIM:617300	HYDROPS FETALIS, NONIMMUNE, AND/OR ATRIAL SEPTAL DEFECT, SUSCEPTIBILITY TO; HFASD	—	—	—
OMIM	OMIM:617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE	—	—	—
OMIM	OMIM:617302	OPTIC ATROPHY 11; OPA11	—	—	—
OMIM	OMIM:617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME; MPSPS	—	—	—
OMIM	OMIM:617304	RETINITIS PIGMENTOSA 77; RP77	—	—	—
OMIM	OMIM:617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD	—	—	—
OMIM	OMIM:617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6; CBAS6	—	—	—
OMIM	OMIM:617315	ANTERIOR SEGMENT DYSGENESIS 6; ASGD6	—	—	—
OMIM	OMIM:617319	ANTERIOR SEGMENT DYSGENESIS 8; ASGD8	—	—	—
OMIM	OMIM:617320	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12; ARCI12	—	—	—
OMIM	OMIM:617321	YAO SYNDROME; YAOS	—	—	—
OMIM	OMIM:617323	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59; MRT59	—	—	—