Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:617571	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14; ARCI14	—	—	—
OMIM	OMIM:617572	EXUDATIVE VITREORETINOPATHY 7; EVR7	—	—	—
OMIM	OMIM:617574	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 13; ARCI13	—	—	—
OMIM	OMIM:617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14	—	—	—
OMIM	OMIM:617576	SPERMATOGENIC FAILURE 18; SPGF18	—	—	—
OMIM	OMIM:617577	CILIARY DYSKINESIA, PRIMARY, 37; CILD37	—	—	—
OMIM	OMIM:617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25	—	—	—
OMIM	OMIM:617585	IMMUNODEFICIENCY 53; IMD53	—	—	—
OMIM	OMIM:617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3	—	—	—
OMIM	OMIM:617592	SPERMATOGENIC FAILURE 19; SPGF19	—	—	—
OMIM	OMIM:617593	SPERMATOGENIC FAILURE 20; SPGF20	—	—	—
OMIM	OMIM:617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES	—	—	—
OMIM	OMIM:617596	MALEYLACETOACETATE ISOMERASE DEFICIENCY; MAAID	—	—	—
OMIM	OMIM:617598	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3; MVA3	—	—	—
OMIM	OMIM:617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55	—	—	—
OMIM	OMIM:617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45	—	—	—
OMIM	OMIM:617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46	—	—	—
OMIM	OMIM:617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM	—	—	—
OMIM	OMIM:617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA	—	—	—
OMIM	OMIM:617605	DEAFNESS, AUTOSOMAL DOMINANT 71; DFNA71	—	—	—
OMIM	OMIM:617606	DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72	—	—	—
OMIM	OMIM:617607	AMELOGENESIS IMPERFECTA, TYPE IIIB; AI3B	—	—	—
OMIM	OMIM:617609	NEPHROTIC SYNDROME, TYPE 15; NPHS15	—	—	—
OMIM	OMIM:617610	POLYCYSTIC KIDNEY DISEASE 5; PKD5	—	—	—
OMIM	OMIM:617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5	—	—	—