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#619927 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 67; MRD67
Gene summaries Genetic tests Medical literature
#618906 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS
#618522 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59; MRD59
Cytogenetic locations: Apoptosis-inducing
#618298 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70; DEE70
Cytogenetic locations: probable
#617991 - CHUNG-JANSEN SYNDROME; CHUJANS
#617796 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 52; MRD52
Cytogenetic locations: ###J##
#616521 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 39; MRD39
CHROMOSOME 2p25.3 DELETION SYNDROME, INCLUDED
Cytogenetic locations: ###F##
#616409 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 33; DEE33
#615282 - CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2
Cytogenetic locations: -
#615075 - NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV
#615074 - GAND SYNDROME; GAND
*615047 - TETRATRICOPEPTIDE REPEAT-, ANKYRIN REPEAT-, AND COILED-COIL-CONTAINING PROTEIN 2; TANC2
*614998 - GATA ZINC FINGER DOMAIN-CONTAINING PROTEIN 2B; GATAD2B
#613765 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9; CMH9
*613084 - MYELIN TRANSCRIPTION FACTOR 1-LIKE; MYT1L
*612870 - PLECKSTRIN HOMOLOGY DOMAIN-INTERACTING PROTEIN; PHIP
*612193 - CARDIOMYOPATHY-ASSOCIATED PROTEIN 5; CMYA5
#612158 - CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 23, WITH OR WITHOUT VENTRICULAR NONCOMPACTION, INCLUDED; CMH23, INCLUDED
#611705 - CONGENITAL MYOPATHY 5 WITH CARDIOMYOPATHY; CMYP5
Cytogenetic locations: ##$###
*610736 - ANKYRIN REPEAT DOMAIN-CONTAINING PROTEIN 23; ANKRD23
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