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#620784 - NEURODEVELOPMENTAL DISORDER PLUS OPTIC ATROPHY; NEDOA
Gene summaries Genetic tests Medical literature
#620783 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 115; DEE115
#620782 - NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT, AUTISM, AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER; NEDLAAD
#620780 - CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE ID; ARCL1D
*620749 - ZINC FINGER PROTEIN 438; ZNF438
#620748 - MEGALENCEPHALY-POLYDACTYLY SYNDROME; MPAPA
#620731 - MICROPHTHALMIA/COLOBOMA 11; MCOPCB11
#620730 - HYPEREMESIS GRAVIDARUM, SUSCEPTIBILITY TO; HG
#620728 - ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1C; UCMD1C
#620726 - BETHLEM MYOPATHY 1C; BTHLM1C
*620720 - ZINC FINGER PROTEIN 549; ZNF549
#620719 - NEURODEVELOPMENTAL DISORDER WITH MOTOR ABNORMALITIES, SEIZURES, AND FACIAL DYSMORPHISM; NEDMSF
#620712 - POLYDACTYLY-MACROCEPHALY SYNDROME; PDMCS
*620706 - DEVELOPING BRAIN HOMEOBOX 2; DBX2
#620700 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 81; MRT81
*620696 - RBPJ-INTERACTING AND TUBULIN-ASSOCIATED PROTEIN 1; RITA1
*620695 - NOTOCHORD HOMEOBOX; NOTO
*620692 - NANOG NEIGHBOR HOMEOBOX; NANOGNB
#620690 - DEVELOPMENTAL DYSPLASIA OF THE HIP 3; DDH3
*620689 - LSM FAMILY, MEMBER 14B; LSM14B
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