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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
#620748 - MEGALENCEPHALY-POLYDACTYLY SYNDROME; MPAPA
#620731 - MICROPHTHALMIA/COLOBOMA 11; MCOPCB11
#620730 - HYPEREMESIS GRAVIDARUM, SUSCEPTIBILITY TO; HG
#620729 - HYPERFERRITINEMIA; HRFT
#620715 - BLEEDING DISORDER, VASCULAR-TYPE; BDVAS
*620695 - NOTOCHORD HOMEOBOX; NOTO
#620690 - DEVELOPMENTAL DYSPLASIA OF THE HIP 3; DDH3
#620683 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 9; FPLD9
*620672 - LEUCINE-RICH REPEAT-CONTAINING PROTEIN 24; LRRC24
#620668 - IMMUNODEFICIENCY 117; IMD117
#620639 - OSTEOGENESIS IMPERFECTA, TYPE XXIII; OI23
#620636 - NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATAXIA AND COGNITIVE DECLINE; CONDCAC
*620604 - PROSTAGLANDIN REDUCTASE 3; PTGR3
#620602 - LYMPHATIC MALFORMATION 14; LMPHM14
*620579 - COILED-COIL DOMAIN-CONTAINING PROTEIN 3; CCDC3
#620558 - CRANIOMETADIAPHYSEAL OSTEOSCLEROSIS WITH HIP DYSPLASIA; CMDOH
Cytogenetic locations: Kif7
#620550 - OPTIC ATROPHY 14; OPA14
Cytogenetic locations: ######
#620542 - NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL RECESSIVE 10; HMNR10
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