Strand list admin 2021-07-15T22:04:20+00:00Search our Test Catalogue Contact Us For assistance with ordering one of our tests call 1-800-1200-695. # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Disorder NamesFabry disease (AGL, ALDOB, ATP7B, COX10, COX6B1, CTNS, EYA1, FAH, FASTKD2, G6PC, GALT, GLA, HPR....)Fabry disease (AGA, AP3B1, ARSA, ARSB, ASAH1, ATP13A2, BLOC1S6, CLN3, CLN5, CLN6, CLN8, CTNS, C....)Familial atrial fibrillation (ABCC9, ACTC1, AKAP9, ANK2, ANK3, CACNA1C, CACNA1D, CACNA2D1, CACNB2, CALM1, CASQ....)Familial juvenile hyperuricemic nephropathy (APRT, CC2D2A, CEP290,CLCN5, COL4A3, COL4A4, COQ2, DCDC2, GLIS2, IFT140, IFT43, I....)Familial partial lipodystrophy (AGPAT2, ALMS1, BANF1, BSCL2, CAV1, CIDEC, CREBBP, EP300, FADD, FAS, FASLG, GNAS,....)Familial transient neonatal hyperbilirubinemia (ABCB11, ABCB4, ABCD3, AKR1D1, AMACR, ATP8B1, BAAT, CYP27A1, CYP7B1, DHCR24, DHCR....)Fanconi renotubular syndrome (HNF4A, SLC2A2, SLC34A1, SLC5A1, SLC5A2....)Fanconi syndrome (ACAD9, ACADL, ACADM, ACADS, ACADSB, ACADVL, ARSA, CLCN5, ETFA, ETFB, ETFDH, OCRL....)Fanconi-Bickel Syndrome (HNF4A, SLC2A2, SLC34A1, SLC5A1, SLC5A2....)Farber lipogranulomatosis (AGA, AP3B1, ARSA, ARSB, ASAH1, ATP13A2, BLOC1S6, CLN3, CLN5, CLN6, CLN8, CTNS, C....)Fatty acid and peroxisomal disorders (ABCD1, ACACA, ACAD9, ACADL, ACADM, ACADS, ACADSB, ACADVL, ACOX1, AGPS, AMACR, CA....)Fazio-Londe disease (ABCD4, ALDH7A1, AMN, BTD, CD320, CUBN, DHFR, FOLR1, GCH1, GGCX, GIF, GPHN, HLCS,....)FG syndrome (ACSL4, ADNP, AFF2, AGTR2, AHI1, ANK3, ANKRD11, AP1S1, AP1S2, AP3B2, ARFGEF2, ARH....)Fish-eye disease (ABCA1, ABCG5, ABCG8, ACAT2, AGPAT2, ANGPTL3, APOA1, APOA2, APOA5, APOB, APOC2, A....)Focal segmental glomerulosclerosis (ACTN4, APOL1, CD2AP, COQ6, INF2*, MYO1E, PAX2, PLCE1, TRPC6....)Folate malabsorption (ABAT, ALDH5A1, ALDH7A1, ATP7A, DBH, DDC, DHFR, FOLR1, GCH1, GLRA1, GLUL, MAOA, M....)Fragile X mental retardation syndrome (ACSL4, ADNP, AFF2, AGTR2, AHI1, ANK3, ANKRD11, AP1S1, AP1S2, AP3B2, ARFGEF2, ARH....)Fragile X-associated tremor/ataxia syndrome (ABCB7, ABHD12, ADCK3, AFG3L2, ANO10, APTX, ATCAY, ATM, ATP13A2, ATP1A3, ATP8A2, ....)Fructose-1,6-bisphosphatase deficiency (AGL, AGXT, ALDOA, ALDOB, ARSB, BTD, DCXR, ENO3, EPM2A, FBP1, FUCA1, G6PC, G6PD, ....)Fructosuria (AGL, AGXT, ALDOA, ALDOB, ARSB, BTD, DCXR, ENO3, EPM2A, FBP1, FUCA1, G6PC, G6PD, ....)Fucosidosis (AGA, AP3B1, ARSA, ARSB, ASAH1, ATP13A2, BLOC1S6, CLN3, CLN5, CLN6, CLN8, CTNS, C....)Fukuyama congenital muscular dystrophy (ANO5, ASAH1, ASCC1, ATP7A, B3GNT1, BAG3, BIN1, BSCL2, CAPN3, CAV3, CHKB, CLCN1, ....)Fumarase deficiency (AARS2, ACAD8, ACAD9, ACADL, ACADM, ACADS, ACADSB, ACADVL, ACAT1, AGK, AIFM1, AMA....)Fallopian tube Cancer (BRCA1, BRCA2, CHEK2, EPCAM, MLH1, MSH2, MSH6, PMS2, PTEN, STK11, TP53....)Familial adenomatous polyposis (FAP) (APC, BMPR1A, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, PMS2, PTEN, SMAD4, STK....)Familial spontaneous pneumothorax (FLCN....)Fanconi anemia (BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FA....)Fetal akinesia deformation sequence/Pena-Shokeir syndrome (ADCY6, B4GALT7, CHRNA1, CHRNB1, CHRND, CHRNG, CHST14, COLEC11, DNM2, DOK7, EFNB1....)Fibrochondrogenesis (ACP5, ACVR1, ADAMTS10, ADAMTS17, ADAMTSL2, AGPS, AIRE, ALG9, ALX4, ANKH, ANKRD11....)Fibrodysplasia ossificans progressiva (ACP5, ACVR1, ADAMTS10, ADAMTS17, ADAMTSL2, AGPS, AIRE, ALG9, ALX4, ANKH, ANKRD11....)Fibular hypoplasia and complex brachydactyly (ACP5, ACVR1, ADAMTS10, ADAMTS17, ADAMTSL2, AGPS, AIRE, ALG9, ALX4, ANKH, ANKRD11....)Focal dermal hypoplasia (CDH3, DLX5, FBXW4, FGFR1, PORCN, TP63, WNT10B, WNT7A....)Frank-ter Haar syndrome (ACP5, ACVR1, ADAMTS10, ADAMTS17, ADAMTSL2, AGPS, AIRE, ALG9, ALX4, ANKH, ANKRD11....)Freeman-Sheldon syndrome (ADCY6, B4GALT7, CHRNA1, CHRNB1, CHRND, CHRNG, CHST14, COLEC11, DNM2, DOK7, EFNB1....)Frontonasal dysplasia (ACTB, ACTG1, ADAMTSL2, AGA, ALX1, ALX4, ARSB, BMPER, CDC6, CDT1, CHST3, COG1, CO....)Fuhrmann syndrome (ARHGAP31, B4GALT7, BMPR1B, COL11A2, COL2A1, COMP, DHODH, DLX5, DOCK6, DYM, ESCO2....)Fumarase deficiency/Hereditary leiomyomatosis (FH....)Familial cylindromatosis (CYLD....)F10 (F10....)F11 (F11....)F12 (F12....)F13A1 (F13A1....)F13B (F13B....)F2 (F2....)F2R (F2R....)F2RL1 (F2RL1....)F3 (F3....)F5 (F5....)F7 (F7....)F8 (F8....)F9 (F9....)FA2H (FA2H....)FAAH (FAAH....)FAAH2 (FAAH2....)FABP1 (FABP1....)FABP2 (FABP2....)FABP3 (FABP3....)FABP4 (FABP4....)FABP6 (FABP6....)FABP7 (FABP7....)FADD (FADD....)FADS2 (FADS2....)FAH (FAH....)FAM120A (FAM120A....)FAM126A (FAM126A....)FAM134B (FAM134B....)FAM161A (FAM161A....)FAM205A (FAM205A....)FAM20A (FAM20A....)FAM20C (FAM20C....)FAM58A (FAM58A....)FAM83H (FAM83H....)FAM8A1 (FAM8A1....)FAM91A1 (FAM91A1....)FANCA (FANCA....)FANCB (FANCB....)FANCC (FANCC....)FANCD2 (FANCD2....)FANCE (FANCE....)FANCF (FANCF....)FANCG (FANCG....)FANCI (FANCI....)FANCL (FANCL....)FANCM (FANCM....)FARS2 (FARS2....)FAS (FAS....)FASLG (FASLG....)FASN (FASN....)FASTKD2 (FASTKD2....)FBLIM1 (FBLIM1....)FBLN1 (FBLN1....)FBLN5 (FBLN5....)FBN1 (FBN1....)FBN2 (FBN2....)FBN3 (FBN3....)FBP1 (FBP1....)FBXL6 (FBXL6....)FBXO10 (FBXO10....)FBXO18 (FBXO18....)FBXO7 (FBXO7....)FBXW11 (FBXW11....)FBXW4 (FBXW4....)FBXW7 (FBXW7....)FCAR (FCAR....)FCER1A (FCER1A....)FCER2 (FCER2....)FCGR1A (FCGR1A....)FCGR2A (FCGR2A....)FCGR2B (FCGR2B....)FCGR3A (FCGR3A....)FCGR3B (FCGR3B....)FCGRT (FCGRT....)FCN2 (FCN2....)FCN3 (FCN3....)FCRL3 (FCRL3....)FDFT1 (FDFT1....)FECH (FECH....)FEM1A (FEM1A....)FEN1 (FEN1....)FERMT1 (FERMT1....)FERMT3 (FERMT3....)FEV (FEV....)FEZF2 (FEZF2....)FFAR1 (FFAR1....)FFAR4 (FFAR4....)FGA (FGA....)FGB (FGB....)FGD1 (FGD1....)FGD3 (FGD3....)FGD4 (FGD4....)FGF1 (FGF1....)FGF10 (FGF10....)FGF14 (FGF14....)FGF2 (FGF2....)FGF20 (FGF20....)FGF23 (FGF23....)FGF3 (FGF3....)FGF8 (FGF8....)FGF9 (FGF9....)FGFBP1 (FGFBP1....)FGFR1 (FGFR1....)FGFR2 (FGFR2....)FGFR3 (FGFR3....)FGFR4 (FGFR4....)FGFRL1 (FGFRL1....)FGG (FGG....)FH (FH....)FHL1 (FHL1....)FHL2 (FHL2....)FIG4 (FIG4....)FIGLA (FIGLA....)FIP1L1 (FIP1L1....)FKBP10 (FKBP10....)FKBP14 (FKBP14....)FKBP5 (FKBP5....)FKBP6 (FKBP6....)FKBPL (FKBPL....)FKRP (FKRP....)FKTN (FKTN....)FLCN (FLCN....)FLG (FLG....)FLNA (FLNA....)FLNB (FLNB....)FLNC (FLNC....)FLT1 (FLT1....)FLT3 (FLT3....)FLT4 (FLT4....)FLVCR1 (FLVCR1....)FLVCR2 (FLVCR2....)FMN1 (FMN1....)FMN2 (FMN2....)FMO1 (FMO1....)FMO2 (FMO2....)FMO3 (FMO3....)FMO4 (FMO4....)FMO5 (FMO5....)FMR1 (FMR1....)FN1 (FN1....)FN3K (FN3K....)FOLH1 (FOLH1....)FOLR1 (FOLR1....)FOXA1 (FOXA1....)FOXA2 (FOXA2....)FOXA3 (FOXA3....)FOXC1 (FOXC1....)FOXC2 (FOXC2....)FOXD3 (FOXD3....)FOXD4 (FOXD4....)FOXE1 (FOXE1....)FOXE3 (FOXE3....)FOXF1 (FOXF1....)FOXF2 (FOXF2....)FOXG1 (FOXG1....)FOXH1 (FOXH1....)FOXI1 (FOXI1....)FOXL2 (FOXL2....)FOXN1 (FOXN1....)FOXP1 (FOXP1....)FOXP2 (FOXP2....)FOXP3 (FOXP3....)FOXRED1 (FOXRED1....)FPGS (FPGS....)FPR1 (FPR1....)FPR2 (FPR2....)FRA10AC1 (FRA10AC1....)FRAS1 (FRAS1....)FREM1 (FREM1....)FREM2 (FREM2....)FREM3 (FREM3....)FRG1 (FRG1....)FRK (FRK....)FRMD6 (FRMD6....)FRMD7 (FRMD7....)FRMPD4 (FRMPD4....)FRY (FRY....)FRZB (FRZB....)FSCB (FSCB....)FSCN2 (FSCN2....)FSHB (FSHB....)FSHR (FSHR....)FTCD (FTCD....)FTH1 (FTH1....)FTHL17 (FTHL17....)FTL (FTL....)FTO (FTO....)FTSJ1 (FTSJ1....)FUCA1 (FUCA1....)FURIN (FURIN....)FUS (FUS....)FUT1 (FUT1....)FUT2 (FUT2....)FUT3 (FUT3....)FUT6 (FUT6....)FUT7 (FUT7....)FUT8 (FUT8....)FUZ (FUZ....)FXN (FXN....)FXYD2 (FXYD2....)FXYD6 (FXYD6....)FYCO1 (FYCO1....)FZD1 (FZD1....)FZD3 (FZD3....)FZD4 (FZD4....)FZD6 (FZD6....)FZD9 (FZD9....)Familial cold autoinflammatory syndrome 2 (ADAM17, CARD14, DNASE1L3, IL10RA, IL10RB, IL1RN, IL36RN, LPIN2, MEFV, MVK, NLRP1....)Familial Mediterranean fever (ADAM17, CARD14, DNASE1L3, IL10RA, IL10RB, IL1RN, IL36RN, LPIN2, MEFV, MVK, NLRP1....)Folate malabsorption, hereditary (ADA, AK2, ATM, B2M, BCL10, BLM, CD247, CD27, CD3D, CD3E, CD3G, CD40, CD40LG, CD8....)Familial male-limited precocious puberty (....)Fraser syndrome (....)
