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*620788 - HIG1 HYPOXIA-INDUCIBLE DOMAIN FAMILY, MEMBER 2A; HIGD2A
Gene summaries Genetic tests Medical literature
*620787 - T-CELL ACTIVATION INHIBITOR, MITOCHONDRIAL; TCAIM
#620784 - NEURODEVELOPMENTAL DISORDER PLUS OPTIC ATROPHY; NEDOA
#620783 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 115; DEE115
#620782 - NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT, AUTISM, AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER; NEDLAAD
*620781 - TRANSMEMBRANE PROTEIN 208; TMEM208
#620780 - CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE ID; ARCL1D
#620779 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 82; MRT82
*620778 - KILLER CELL IMMUNOGLOBULIN-LIKE RECEPTOR, THREE DOMAINS, SHORT CYTOPLASMIC TAIL, 1; KIR3DS1
#620777 - PULMONARY HYPERTENSION, PRIMARY, 6; PPH6
#620776 - THROMBOCYTOPENIA 13, SYNDROMIC; THC13
#620775 - NEUROMUSCULAR DISORDER, CONGENITAL, WITH DYSMORPHIC FACIES; NMDF
#620774 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 114; DEE114
#620772 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 113; DEE113
*620770 - MITOREGULIN; MTLN
*620769 - HYDROXYACYL-THIOESTER DEHYDRATASE, TYPE 2; HTD2
*620768 - RIBOSOME-BINDING FACTOR A; RBFA
#620767 - SECKEL SYNDROME 11; SCKL11
*620766 - FORMATION OF MITOCHONDRIAL COMPLEX V ASSEMBLY FACTOR 1 HOMOLOG; FMC1
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