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#620782 - NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT, AUTISM, AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER; NEDLAAD
Gene summaries Genetic tests Medical literature
#620780 - CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE ID; ARCL1D
#620777 - PULMONARY HYPERTENSION, PRIMARY, 6; PPH6
#620774 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 114; DEE114
#620771 - JEFFRIES-LAKHANI NEURODEVELOPMENTAL SYNDROME; JELANS
#620755 - GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 12; GEFSP12
#620748 - MEGALENCEPHALY-POLYDACTYLY SYNDROME; MPAPA
#620746 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CHARACTERISTIC BRAIN ABNORMALITIES; NEDHBA
*620742 - INTRAFLAGELLAR TRANSPORT 70B; IFT70B
*620741 - INTRAFLAGELLAR TRANSPORT 70A; IFT70A
*620740 - STATHMIN 4; STMN4
#620731 - MICROPHTHALMIA/COLOBOMA 11; MCOPCB11
#620730 - HYPEREMESIS GRAVIDARUM, SUSCEPTIBILITY TO; HG
#620728 - ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1C; UCMD1C
#620727 - ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1B; UCMD1B
ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1A/1B, DIGENIC, INCLUDED; UCMD1A/1B, DIGENIC, INCLUDED
#620726 - BETHLEM MYOPATHY 1C; BTHLM1C
#620725 - BETHLEM MYOPATHY 1B; BTHLM1B
#620722 - DEAFNESS, AUTOSOMAL DOMINANT 90; DFNA90
#620719 - NEURODEVELOPMENTAL DISORDER WITH MOTOR ABNORMALITIES, SEIZURES, AND FACIAL DYSMORPHISM; NEDMSF
#620715 - BLEEDING DISORDER, VASCULAR-TYPE; BDVAS
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