Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50	—	—	—
OMIM	OMIM:617788	MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51	—	—	—
OMIM	OMIM:617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52	—	—	—
OMIM	OMIM:617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53	—	—	—
OMIM	OMIM:617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54	—	—	—
OMIM	OMIM:617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19	—	—	—
OMIM	OMIM:617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA	—	—	—
OMIM	OMIM:617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL	—	—	—
OMIM	OMIM:617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3	—	—	—
OMIM	OMIM:617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW	—	—	—
OMIM	OMIM:617808	COFFIN-SIRIS SYNDROME 6; CSS6	—	—	—
OMIM	OMIM:617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3	—	—	—
OMIM	OMIM:617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15	—	—	—
OMIM	OMIM:617816	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16; GPIBD16	—	—	—
OMIM	OMIM:617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR	—	—	—
OMIM	OMIM:617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2	—	—	—
OMIM	OMIM:617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS	—	—	—
OMIM	OMIM:617825	GLUCOCORTICOID DEFICIENCY 5; GCCD5	—	—	—
OMIM	OMIM:617827	IMMUNODEFICIENCY 55; IMD55	—	—	—
OMIM	OMIM:617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2	—	—	—
OMIM	OMIM:617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58	—	—	—
OMIM	OMIM:617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55	—	—	—
OMIM	OMIM:617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM	—	—	—
OMIM	OMIM:617839	AMYOTROPHIC LATERAL SCLEROSIS 23; ALS23	—	—	—
OMIM	OMIM:617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56	—	—	—