Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26	—	—	—
OMIM	OMIM:616059	MIRROR MOVEMENTS 3; MRMV3	—	—	—
OMIM	OMIM:616060	BLOOD GROUP, DOMBROCK SYSTEM; DO	—	—	—
OMIM	OMIM:616063	POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE; POROK8	—	—	—
OMIM	OMIM:616067	46,XY SEX REVERSAL 9; SRXY9	—	—	—
OMIM	OMIM:616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2	—	—	—
OMIM	OMIM:616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29	—	—	—
OMIM	OMIM:616079	RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES; RDGCA	—	—	—
OMIM	OMIM:616080	MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE; MCPH12	—	—	—
OMIM	OMIM:616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C	—	—	—
OMIM	OMIM:616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30	—	—	—
OMIM	OMIM:616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD	—	—	—
OMIM	OMIM:616087	DIABETES MELLITUS, NONINSULIN-DEPENDENT, 5; NIDDM5	—	—	—
OMIM	OMIM:616089	BLOOD GROUP, GERBICH SYSTEM; GE	—	—	—
OMIM	OMIM:616093	BLOOD GROUP, ABO SYSTEM	—	—	—
OMIM	OMIM:616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12	—	—	—
OMIM	OMIM:616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D	—	—	—
OMIM	OMIM:616098	IMMUNODEFICIENCY 37; IMD37	—	—	—
OMIM	OMIM:616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH	—	—	—
OMIM	OMIM:616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5	—	—	—
OMIM	OMIM:616106	PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO; PSORS15	—	—	—
OMIM	OMIM:616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS	—	—	—
OMIM	OMIM:616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9; MC3DN9	—	—	—
OMIM	OMIM:616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS	—	—	—
OMIM	OMIM:616115	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4; FCAS4	—	—	—