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Cardiomyopathy
Mayo_clinic
Overview Cardiomyopathy (kahr-dee-o-my-OP-uh-thee) is a disease of the heart muscle that makes it harder for the heart to pump blood to the rest of the body. Cardiomyopathy can lead to heart failure. The main types of cardiomyopathy include dilated, hypertrophic and restrictive cardiomyopathy. Treatment — which might include medications, surgically implanted devices, heart surgery or, in severe cases, a heart transplant — depends on the type of cardiomyopathy and how serious it is. Types Symptoms There might be no signs or symptoms in the early stages of cardiomyopathy. But as the condition advances, signs and symptoms usually appear, including: Breathlessness with activity or even at rest Swelling of the legs, ankles and feet Bloating of the abdomen due to fluid buildup Cough while lying down Difficulty lying flat to sleep Fatigue Heartbeats that feel rapid, pounding or fluttering Chest discomfort or pressure Dizziness, lightheadedness and fainting Signs and symptoms tend to get worse unless treated.PLN, TNNT2, MYBPC3, DMD, TNNI3, TNF, DES, SGCD, CRYAB, TAZ, EMD, MYH7, PRKAG2, DSP, PKP2, TTN, TTR, LAMP2, VCL, CSRP3, DSG2, ACTC1, TPM1, DSC2, RYR2, MYL2, GLA, RBM20, MYPN, NEXN, SGCB, POLG, TMEM43, MYOT, JPH2, EPG5, JUP, MYL3, LDB3, AGT, ABCC9, MYH6, SCN5A, SCO2, GAA, TNNC1, IL6, SOD2, MAPK3, CAV3, SLC22A5, IL1B, STAT3, CAT, LPL, HGF, PTPN11, PSEN1, NDUFS2, ANKRD1, TMEM70, MAPK1, IL1A, PRKAA2, FKTN, ATF3, CASQ2, MAPK14, IL4, CBR1, TLR2, RAF1, ACTN2, FASLG, RIT1, ITGB1, LIMS2, OLR1, NDUFV2, PARP1, MAP2K1, SOS1, ADRB2, EDN1, TCAP, AKT1, EPO, MYOZ2, PPP1R1A, APP, PPARD, GRK2, ADORA2A, TRIM63, ADCY5, COX1, POMC, CS, THPO, CYP2C9, ADCYAP1, MYOCD, HRAS, HSPE1, HSPD1, NPPB, MAPT, NEBL, MAP2K2, YWHAH, GATAD1, MAPK11, BRAF, KRAS, LAMA4, LDHA, BDKRB2, AVPR2, AVP, PRKCE, RHOJ, NRAS, PDK2, DTNA, FAS, MAP3K5, PTGS2, REEP1, PDLIM3, AQP2, PPARGC1A, NOS1, IFNG, TXN, UTS2R, RAD51, CCL2, ITGA7, NOS3, MIF, ADAM10, ACSL1, PDE2A, IGF1R, FKBP1B, FLNC, LRP1, LMNA, GOT1, FXN, TP53, ATP5F1B, XDH, TIMP2, UTS2, CASR, FHL1, HADHA, PNPLA2, ALPK3, GYG1, HFE, FKRP, SYNE2, HADHB, NPPA, VCP, CPT2, KCNQ1, ANO5, COX15, SDHD, POMT1, ATP6, GBE1, IDH2, MYO18B, GYS1, IDUA, DCAF8, MMUT, MPLKIP, C1QBP, AGL, TRIP4, HAMP, USP9X, DPM3, NEB, TPM3, PEX13, H19-ICR, PEX14, SLC40A1, BMP2, CENPE, RMRP, SLC25A20, GNE, GMPPB, SLC25A42, TPM2, CLPB, PEX7, HPS1, HNRNPA2B1, HNRNPA1, MIPEP, PEX16, IGF2, CDKN1C, ARSB, CDH23, WFS1, PEX10, KCNH1, POMT2, AQP4, XK, PEX19, GTF2H5, H19, PEX5, ACADS, ACTA1, RNF113A, KLHL41, KBTBD13, LAMA2, USP8, CEP85L, ACTB, UQCRFS1, PEX2, PEX6, RRM2B, PEX26, TK2, RAB3GAP2, PEX1, TTN-AS1, ALG1, KCNQ1OT1, AIP, GPC4, TFR2, TRNT, ACE, POMGNT1, NEU1, ERCC3, D2HGDH, ERCC2, PHYH, DLD, AHCY, ATAD3A, PCCB, AQP4-AS1, BAG3, PEX11B, GABPA, VAC14, PMM2, CISD2, PCCA, POMK, HBB, DSG2-AS1, SCN1B, GUSB, GTF2E2, GSN, GTPBP3, NFE2L2, RNASEH1, LTBP4, MYLK2, PEX12, PEX3, RPL36A-HNRNPH2, ABHD5, FIG4, GPC3, PPARA, CALR, GJA1, UTRN, PIK3CA, MYO6, SLC25A4, MGAM, CALCR, IGF1, CCR5, ILK, DECR1, SLC6A8, TGFB1, SI, PIK3CD, MEF2A, PIK3CG, PIK3CB, TRPV2, SIRT3, ADRB1, PRL, FGF21, LGALS3, S100A1, GATA4, TAC1, NLRP3, SLC5A1, SYNE1, EGFR, PPARGC1B, CYBB, HJV, CTNNB1, TLR3, NKX2-5, CSF3, BEST1, DNM1L, RND3, APRT, PRPF6, AARS2, KL, MBL2, REN, MFAP1, GH1, ACAD9, MYOF, HLA-DRB1, IL18, ADIPOQ, HIF1A, GLB1, S100B, PDE5A, VEGFA, HGS, MAPK8, PGM1, PRKCA, MASP2, RBCK1, GDF15, VIP, DENR, SSPN, APLN, TSFM, KEAP1, CTNNA3, MFN2, TLR4, MTO1, HSPB7, SDS, SDHB, SRSF5, PLEC, DAPK2, RBFOX2, SLC5A2, MLYCD, SIRT1, SLN, PPARG, TNNI3K, SUMO2, SORD, BSCL2, TAB2, ROS1, RIPK3, PPA2, TFAM, TRNT1, NAT2, TNC, MTFMT, DUSP4, COL3A1, SHROOM3, MYH7B, ERBB2, KLK1, ACE2, EYA4, PRDM16, RERE, RBM45, ESRRB, HSPB6, IL17A, MIR29C, ATN1, APOO, GNPTAB, IL1RN, CCN1, CYP2D6, FHL2, FHOD3, HMOX1, FOXO3, SESN2, MTOR, G6PD, COA6, MIR146A, RBFOX1, LCN2, MTTP, MYH2, COX2, ND1, MIR499A, SLC25A5, DMPK, CCR2, SARDH, ALDH2, ACTA2, ACADVL, NGF, NOS2, DAG1, CYP1A1, ALAS2, HARS1, DNAH8, NR3C2, RBM24, CRMP1, BIN1, CPT1A, CMYA5, SLCO1B1, THEMIS, HEXIM1, SENP5, TPCN2, CAVIN1, LINC-PINT, PIKFYVE, GOLGA6A, BOLA3, PDLIM5, HPSE, MARCHF8, LRRC10, NDUFS7, CHCHD10, GSTK1, PPP1R13L, SOX2-OT, JMJD1C, MPEG1, MYL12A, CD300C, PDE10A, CELF1, CAVIN4, FNDC5, TLR9, MIR122, ARFGEF2, HDAC6, MIAT, USP15, MIR323A, COA5, MIR378A, MIR424, MIR448, ELMO1, H4C15, BMS1, MIR410, SART3, RGS6, ADAMTS2, SDHAF1, HOTAIR, CHST3, HAND2, ABCG2, AK6, HAND1, MHRT, HDAC5, TNFSF12-TNFSF13, ABCC5, MIR29B1, MIR155, MIR18A, MIR195, MIR21, MIR221, MYL9, MIR23B, TUBA1B, MIR29A, MICU1, UBE4B, ABCB6, MIR29B2, EBI3, NAMPT, BCAP31, MIR320A, KIF20A, PPIF, MIR34A, ACTR2, MIR34B, EHD1, TBC1D1, UBR1, BTNL2, UBQLN1, MDFIC, EMC7, CELF4, CHPT1, LRRC7, SENP1, CD274, ALS2, CACNG8, SENP2, SLC28A3, MYLIP, UBE2T, ASTE1, TMBIM1, NOD2, MCAT, MTMR14, MARCKSL1, HPGDS, TWNK, TAX1BP3, IMMT, ERBIN, TRPM4, KLHL24, SNRK, RMND1, TNFRSF12A, COQ4, STX17, MOCOS, RCBTB1, CHDH, STAP2, FIS1, TRMU, AGK, DCAF6, IRX4, BEX1, TMEM126B, NOX3, ZC4H2, ANGPTL8, FSD1, MYH14, CACYBP, LAMP3, CALR3, ZFPM2, LRRC39, UFL1, DNAJC19, SPATA18, EMB, SLCO6A1, MGA, WDTC1, DKK1, RAB3GAP1, ISM2, MLXIP, STK38, UNC45B, ADAMTS13, LIAS, AMOTL1, XIRP1, NLRP6, H4-16, NNT, FBXO32, EVA1A, EHMT1, PANK2, PPP1R2C, LATS2, ITCH, FSD1L, TSSK1B, FBXL4, LDLRAP1, TOR1AIP1, PRRT2, MLIP, PART1, MYLK3, TIMM50, FNIP1, TGS1, MYL12B, EGLN3, SMUG1, TBX20, RPS27, LONP1, GFAP, GFI1, GNB3, GRK5, GPX3, GSK3A, GTS, GZMB, HAS3, HTT, HDAC2, HLA-B, HLA-C, HLA-DPB1, HMGB1, HSF2, GFER, FUT4, HSPA8, FOSL2, ECHS1, EDNRA, EDNRB, EPHB2, ESRRA, FAAH, FABP4, FABP3, FANCC, FANCF, FAP, FBN1, FGA, FGFR4, FOXO1, HSPA5, HSPB1, MME, KCNMA1, KDR, KNG1, LEP, LEPR, LORICRIN, LOXL2, LSAMP, SH2D1A, MAFD2, MATN1, SMCP, MEF2C, MEFV, MEIS1, MGAT1, KCNN3, KCNJ2, HSP90AA1, KCNH2, ICAM1, IGHG3, IL2RA, IL4R, IL7, IL10, IL12B, IL13, IL15, CXCL10, ISG20, ITGAM, ITGAX, ITGB6, KARS1, DUSP1, DSG1, DPYD, APOA1, APOE, ARSD, ARVD3, ATP2A2, AVPR1A, BDNF, BPI, BRCA1, BRCA2, C3, C5, C5AR1, VPS51, CA2, CAD, APOB, BIRC5, DPP4, APCS, ABL2, ABR, ACACA, ADAM8, ADM, ADPRH, ADRA1D, ADRA1A, ADRB3, AGTR1, AKT2, AKR1B1, ANGPT2, ANPEP, ANXA1, CASP1, CASP3, CBR3, CCNT1, CREM, CRP, CSNK2A2, CCN2, CTSB, CTSD, CTSL, CUX1, CYP2C19, CYP2E1, CYP19A1, CYP27B1, DCN, DIO2, DNM2, CR1, COX6B1, COMP, CDK2, CD34, CD36, SCARB1, SCARB2, CD69, CDH2, CDK9, COL4A1, CFL1, CFL2, CFTR, CMA1, CNR1, COL1A1, MLF1, MMP1, CD163, TFAP2A, THBS4, TIMP1, TIMP3, TJP1, TMPO, TRAF3, TRAF6, TRPC3, TRPM2, TSHR, TTK, TYK2, UBE3A, UCP2, VAV1, THBS3, PRDX2, VEGFB, TCF7L2, SLC18A3, SMARCA4, SMPD1, SUMO3, SOX2, SPARC, SPN, SPP1, SRI, SRF, SST, SULT1E1, STIM1, STRN, TACR1, VDR, WNT1, MMP9, H4C5, H4C14, LOH19CR1, ATRN, TP63, BECN1, TNFSF12, NRP1, CCN5, KAT2B, PER2, GYG2, SPAG9, IL1RL1, MSC, TSPOAP1, H4C13, H4C2, YWHAE, H4C8, ZBTB17, ALMS1, CXCR4, TFEB, FGF23, TCL1A, SLC14A2, DYSF, H4C9, H4C1, H4C4, H4C6, H4C12, H4C11, H4C3, SLC9A1, SLC8A1, SIX1, NPR1, PAH, SERPINE1, PCBP1, SERPINA5, PCMT1, PCNT, PDCD1, PDK4, PGC, PGK1, ABCB1, SLC25A3, PIM1, PKP1, POLR2A, OXTR, CCN3, ST3GAL4, NDUFS6, MMP14, MPO, MRE11, MST1, MT1B, CYTB, ND4, RNR2, TRNV, MUC2, MYBPC2, GADD45B, MYL4, NAGA, NDUFA5, PON1, PPA1, PPIA, PPID, RNASE4, ROCK1, RPL32, RPS19, AARS1, S100A6, S100A8, S100A9, SCD, SCO1, SDHA, SELP, SGCA, SGCG, SGSH, RLN2, RGS2, RAC1, MAPK7, PRH1, PRH2, PRKAA1, PRKAB1, PRKCB, PRKG1, MAP2K6, RAB6A, PSEN2, PTEN, PTH, PTHLH, PTPRC, RAB1A, SIRT1-AS
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Abortion In Nebraska
Wikipedia
American Economic Journal: Applied Economics . 3 : 189–223. doi : 10.1257/app.3.1.189 . Abortion in the United States by state States Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming Federal district Washington, D.C.
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Splenomegaly
Wikipedia
This article needs additional citations for verification . Please help improve this article by adding citations to reliable sources . Unsourced material may be challenged and removed. Find sources: "Splenomegaly" – news · newspapers · books · scholar · JSTOR ( February 2010 ) ( Learn how and when to remove this template message ) Splenomegaly CT scan in a patient with chronic lymphocytic leukemia , showing splenomegaly. Yellow arrows point at the spleen . Specialty General surgery Splenomegaly is an enlargement of the spleen . [1] The spleen usually lies in the left upper quadrant (LUQ) of the human abdomen . Splenomegaly is one of the four cardinal signs of hypersplenism which include: some reduction in number of circulating blood cells affecting granulocytes , erythrocytes or platelets in any combination; a compensatory proliferative response in the bone marrow; and the potential for correction of these abnormalities by splenectomy . Splenomegaly is usually associated with increased workload (such as in hemolytic anemias ), which suggests that it is a response to hyperfunction.OCLN, NRAS, HBB, PEPD, XIAP, KRAS, APOE, FAS, CYP1A2, KCNN3, STAT5B, NFE2L2, BDKRB1, FLT3, EIF2AK1, MECOM, NOTCH1, APC, AHR, MAPT, PSEN1, APP, DNASE2, TYMS, ABCB11, STX11, TNFSF11, ALMS1, TNFSF12, TNFRSF11A, ZAP70, AP3B1, GFI1B, DPM1, UROS, KLRC4, ABCA1, AP3D1, SH2B3, NPC2, AGPAT2, RNASEH2A, SEC23B, TCIRG1, RASGRP1, GNE, PLEKHM1, SLC7A7, PIEZO1, LPIN2, TTC37, SEC24C, ADAMTS3, UMPS, CLDN1, CYP7B1, TNFRSF1B, UFD1, TNFRSF4, SOX10, SMPD1, SLCO2A1, SLC4A1, SLC2A1, SKIV2L, SGSH, ATXN2, RREB1, RMRP, RHAG, RAG2, RAG1, RAB27A, PEX2, ABCD3, PTPRC, SPTA1, SPTB, AKR1D1, THPO, HIRA, TPP2, TPI1, TP53, VPS45, TNFRSF1A, TLR4, TGFB1, STAT4, TERT, TERC, TCF4, TBXAS1, TBX1, TALDO1, NEK4, KLF1, TNFRSF13B, DOLK, USB1, C15orf41, CARD11, CCDC115, ITCH, FERMT3, HSD3B7, ALPK1, CTC1, FAT4, NLRP1, CYBC1, GNPTAB, DDRGK1, VPS33A, DCLRE1C, ABCG8, ABCG5, NOD2, COX4I2, TMEM67, COG7, G6PC3, RNU4ATAC, NCF1, GPIHBP1, UBAC2, SUMF1, CAVIN1, JMJD1C, SAMD9L, IL23R, HJV, CCBE1, CDAN1, LACC1, HGSNAT, TNFRSF13C, NLRP3, PIGM, BACH2, NLRC4, HAMP, RTEL1, DCDC2, GLRX5, SBDS, FOXP3, SNX10, ICOS, OSTM1, LAT, BSCL2, SLC17A5, TINF2, IFT172, PSMB9, SF3B1, RPGRIP1L, VPS13A, NBEAL2, DYNC2LI1, ERAP1, CC2D2A, ADA2, WDR35, COG6, SCYL1, INPP5E, BTNL2, ALG1, NGLY1, NHP2, CHD7, SLC39A4, SLC30A10, NOP10, SLC29A3, STEAP3, WRAP53, MKS1, TET2, PTEN, PIK3R1, PSMB8, PSMB4, DKC1, DHCR24, DGUOK, CYBB, CYBA, CTSK, CTNS, CTLA4, CR2, CPOX, COMT, COL2A1, CCR1, CLCN7, ERCC8, LYST, CD81, DNASE1L3, EPB41, EPB42, G6PC, GLB1, GPC3, GBA, GATA2, GATA1, GALE, GAA, FUCA1, ERBB3, FOS, FMO3, FGA, GPC4, FAH, F5, ERCC6, CD40LG, SCARB2, CD28, FASLG, ATP7B, ATP6AP1, ATP6V1B2, ATM, ASAH1, ARVCF, ARSB, APOC2, B2M, APOA1, ANK1, ALDOA, ALAS2, AKT1, AGA, ADA, ATRX, CCND1, CD27, CALR, MS4A1, CD19, RUNX1, CAV1, CASR, CASP10, CASP8, CA2, BCL2, C4A, BTD, BRAF, BPGM, BMP2, BCR, BCL6, GNS, GP1BA, GP1BB, GPC1, NOTCH2, NFKB2, NFKB1, NEU1, NCF4, NCF2, NAGLU, MYD88, MVK, MMUT, MST1, MPL, MIF, MEFV, MCM4, MAN2B1, LYZ, PNP, OTC, PARN, PIK3CD, PSAP, PRKCD, PRF1, PPARG, PKHD1, PKLR, ABL1, PIK3CA, PDGFRA, PIK3C2A, PHYH, PHKG2, PHKA2, ABCB4, ATP8B1, PEX7, SH2D1A, LPL, IGH, HFE, IDUA, IDS, IRF8, HPGD, HLA-DRB1, HLA-B, HK1, HBG2, LMNA, HBG1, HBA2, HBA1, GYPC, GUSB, GPR35, GPI, IFNGR1, IL12A-AS1, IL1RN, IL2RA, LIPA, LIG4, LCAT, LBR, KCNN4, KCNH1, JAK2, ITK, INPPL1, IL12A, IL10, IL7R, IL6, IL2RG, IL2RB, HLA-DQB1, VEGFA, TNFRSF8
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Anxiety Disorders
Mayo_clinic
Overview Experiencing occasional anxiety is a normal part of life. However, people with anxiety disorders frequently have intense, excessive and persistent worry and fear about everyday situations. Often, anxiety disorders involve repeated episodes of sudden feelings of intense anxiety and fear or terror that reach a peak within minutes (panic attacks). These feelings of anxiety and panic interfere with daily activities, are difficult to control, are out of proportion to the actual danger and can last a long time. You may avoid places or situations to prevent these feelings. Symptoms may start during childhood or the teen years and continue into adulthood. Examples of anxiety disorders include generalized anxiety disorder, social anxiety disorder (social phobia), specific phobias and separation anxiety disorder.SLC6A4, HTR7, NPY1R, CRHR1, FMR1, APP, CRP, DRD2, CRH, NPS, CNR1, TNF, NPY, ADORA2A, SLC6A3, GLO1, CACNA1C, CARTPT, MECP2, DISC1, CRHR2, SERPINA1, GABRA2, FOS, GRM8, MIR34A, MIF, UCN, SHANK1, CHRNA5, MAPT, DIXDC1, MAGI2, TAFA2, HTR1A, OXT, TG, CHRNB2, RAI1, GNB1, EOMES, IFNA2, PAM, DNMT1, MDK, HTR2C, ESR2, HTR1B, AVPR1B, HDAC2, HCN1, L1CAM, ADRA2A, KDM3B, DNMT3B, NCOR1, PDE4B, LINC02085, TAL1, GAD2, NPSR1, OR8A1, ESR1, GAD1, ARSI, NR3C1, COMT, SUOX, FAAH, TPH2, OXTR, RAD51, PTPRT, FKBP5, COPD, GIGYF2, SDK1, CNGB3, KLK3, AVP, OPN1SW, BDNF, MFAP3L, ATF7IP, ZFHX3, SCLY, APOE, IL1B, ARSD, SOX13, IL6, MAOA, LTBP3, ADCY2, KRT7, CCK, EDIL3, LEP, CECR, LINC02210-CRHR1, POMC, GAL, TAC1, BRCA1, GRM5, RGS2, HCRT, HTR2A, IL10, LOC110806262, TSPO, SMS, WASF2, SIRT1, PSS, WASF1, DRD4, C1QL1, SNCA, STX2, CYP2D6, SMIM20, CHRNA4, SMCP, TSPAN31, NANS, TMEM132D, NGF, ZC4H2, AMY1A, DTNBP1, MOCOS, INSRR, THAS, AMY1B, PAEP, AMY1C, ALDH2, CLOCK, IGF1, BCHE, ADIPOQ, NR3C2, COPE, ACACA, CFP, HCRTR1, OPRM1, NUCB2, ACAD8, HSD11B2, FGF2, PRL, NOS1, EDN1, BMS1, ADCYAP1, RLN3, ELK3, WAS, ADRA2B, DBI, CCKBR, APLN, GALR2, GTF2I, CALM1, CALM2, CALM3, ACKR3, HTT, CNR2, TPH1, MZB1, GER, GPR42, P2RX7, TACR1, CTNNB1, SERPINE1, SERPINB2, SNAP91, MCIDAS, BDNF-AS, CXCL8, ASIC1, LPAR2, ADCYAP1R1, ADH1B, ADRA1A, IDO1, AGT, TBX4, BRS3, BAG3, ANK3, MME, PICALM, HTR3A, SSTR4, BRCA2, GLI2, PKD2L1, EBPL, CYP2C19, PROS1, WASF3, OSR1, DRD3, PDSS1, SEPHS1, PVALB, FLT4, EDNRA, DNASE1L3, SST, SAT1, CXCR6, GCG, SGCE, MS, SHBG, MMP9, NR1D1, IKBKE, PTMAP4, MSMB, PTGS2, WDHD1, YWHAE, PSMD9, LEPR, PTMA, ADAMTS2, LPP, NPEPPS, REST, BTG3, SGCA, S100B, PER3, ENDOU, MCL1, MC4R, MGLL, CCL3, MC1R, CNTN3, SLC1A1, COX2, NTF3, CACYBP, TP53, TLR2, S100A10, SOD1, TIA1, SMR3A, TH, RAPGEF3, ABCB1, RBM14, FST, PAFAH1B1, KANK2, STAT3, NTRK2, ALYREF, ARC, SLC18A2, TSKU, MAPK8, MAPK3, PSAT1, NFKB2, SLC6A1, SLC6A2, UMOD, UGT2B15, SF3B1, TSC2, TRPM2, PLAG1, NPC1, APOBEC3C, SDS, STIN2-VNTR, STMN1, BCL2, SLC17A8, ANKK1, GHSR, CREB1, CPP, PINK1, DCLRE1C, GPER1, PHOBS, GRN, DLGAP3, GSK3B, MIR219A1, GSTM1, CASP1, MDD1, CALCA, GDNF, CTNND2, GABRG2, FKBP4, TP53INP1, UCN3, UBXN11, DMTN, NLRP3, EXOSC6, FGD1, TSACC, GABRA6, RSS, ACE, DBH, SPX, DAO, OR2AG1, ASXL1, MIR488, GRIA1, IFNG, ARSA, IL18, HTR6, CFI, RBM14-RBM4, FAS, IL1A, AR, AGTR1, IGFBP2, ACHE, AVPR1A, MTCO2P12, TET2, CD226, TAOK2, LOC102723971, FGFBP3, NRG3, CENPV, HOMER2, PGR-AS1, PWAR1, CBLN4, CBLN2, CAMKK2, ZNF92, QKI, CPLX1, BPIFA2, SLC26A1, SYNGR1, SLC33A1, BATF2, FMR1-IT1, FASTK, CPSF4, LRRK2, INO80C, CERNA3, SLC32A1, HPSE, PDE10A, GPR55, ALDH1L1, TEMPS, LYPD6, HOMER1, TAAR1, SLCO1B1, SART3, GNLY, MIR4717, CCR2, MIR124-1, MIR137, FAAHP1, TENM1, MIR663A, MIR15A, MIR579, MIR22, HCN4, CASP8AP2, CCS, RBM8A, MIR34B, MIR330, LINC00273, MIR338, PPM1F, MBOAT4, MIRLET7D, GPHN, CIT, LAMA1, C9orf72, HDAC4, UNC13B, CACNA1G-AS1, NXF1, MAGED1, GPNMB, NPAS4, LINC01672, BCAR1, CITED2, MT1DP, SIGMAR1, NANOS1, RIDA, TMEM59, MALAT1, ZGLP1, RAPGEF4, NLGN4Y, PRDM6, ADIPOR1, SLC50A1, FOXP3, KCNIP3, CTNNBL1, SLC2A9, LXN, PADI1, CD274, SLC17A7, PYCARD, FLVCR1, PELI1, REM1, NDRG2, DLL1, CASKIN1, NLGN2, PCSK1N, HPGDS, PDE7B, GRHL3, ZNF462, B3GAT1, SND1, NPTN, GABRQ, ZDHHC9, CD160, LEF1, CCHCR1, NLGN3, AHI1, NDE1, CC2D1A, TLR9, ADA2, ULK4, CDCA8, BLOC1S4, CHDH, AIFM1, IFT122, MBD5, ALLC, INPP5K, GHRL, ASB1, RASD1, SIRT6, CENPJ, EAF2, RXFP3, TLR7, USE1, GOLPH3, SIL1, PTPN22, CIAO3, SYNE1, SLC38A1, ARHGEF9, DOCK8, NBEAL2, KDM6B, PHF8, TTLL5, ARHGAP24, IGSF9B, TSSK1B, TPX2, TMPRSS13, DKK1, NLRP1, ASCC2, P4HTM, KISS1R, PPP1R9B, PHB2, CAPS2, LMLN, CREB3L1, PARK7, ZNF804A, PPP1R2C, TET1, CPED1, EFHD2, CPEB1, PDIA2, RAPH1, UBE2Z, DLK2, SLITRK5, DUSP26, SOSTDC1, PART1, NIPBL, TPSG1, FBXO7, NCS1, PANX1, PRND, TSSK2, PAGR1, SLC52A2, SMUG1, SEC14L2, MANEA, OTP, EHMT1, TARDBP, ZDHHC7, ABAT, SELENBP1, FOXG1, FLNB, FOLH1, FRAXA, FSHMD1A, NR5A1, GAST, GABPA, GABRA5, GALNS, GATA4, GFAP, GHRH, CBLIF, GJB2, GLI3, FLNA, FGFR3, GNAS, FGF9, ENPEP, EP300, EPHA5, EPHB1, EPHB2, EPRS1, ERBB4, EYA1, EZH2, F2R, F9, FAP, FBN1, FDPS, FES, GLP1R, GNRHR, BAIAP3, HOXD13, HES1, HSPA1B, HSPG2, IGF2, IGFBP3, IL1RN, IL2, IL13, IL15RA, IL17A, IRF6, JAG2, JAK2, KCNS1, KIF22, HRAS, HOXB8, MCHR1, HNRNPU, GPR26, GPX4, GRIA2, GRIK1, GRIN2B, GRP, GSR, GSTP1, GSTT1, GUCY2C, GYPA, CFH, NRG1, HLA-B, HMGN1, ENO1, EIF4EBP1, EIF4E, ATM, BNIP3, BPI, SERPING1, VPS51, CAMK2G, CAPN1, CAST, CASP2, CAT, CCKAR, CD6, CD34, CDK5, CDKN2A, CGA, B2M, AQP6, EEF1A2, APC, ADM, ADORA1, PARP1, ADRB2, AGRP, AGTR2, ALAD, ALB, ALDH1A1, ALOX15, ALPL, AMD1, AMD1P2, ANGPT2, AOAH, CHGA, CHRM3, CHRNA2, CHRNA7, CYP1A2, CYP2B6, CYP2E1, CYP17A1, DAP, DCX, DDC, AKR1C1, DIO3, DLX4, DPYSL2, DRD1, RCAN1, DUSP2, DYRK1A, CYBB, CUX1, CTRL, CPM, CISH, CNP, CNTF, KLF6, CORT, CPD, CREM, CSTA, CRHBP, CRY1, CRY2, CRYGD, CSF1, CSF1R, KPNA1, KTN1, LCN2, PMEL, SLC1A3, SLC22A2, SMPD1, SRC, SRD5A1, STXBP3, SYP, TACR3, TCN1, TCOF1, TDO2, NR2F1, TGFA, TGFB1, THOP1, SLC1A2, SET, RAC1, SDHD, REN, RGS1, RIT1, RORA, RPE65, RPS4Y1, RPS19, RYR1, S100A1, S100A12, SCN1A, SCT, CCL4, CCL11, CXCL12, TIMP1, TNFAIP3, TP73, TPO, SYN3, LOH19CR1, SRPX, GALR3, CPZ, MKNK1, USO1, NPFF, PSMG1, AKR1C3, CES2, TMEM11, NR1I2, SPHK1, MBD2, DGCR6, BAS, MIA, NR1H2, TRH, TRPC5, TTC1, TTN, TWIST1, TYMS, VHL, FXR1, VIP, TRPV1, LAT2, XK, YY1, GHS, REG1A, PTPRZ2, LGALS3, MYD88, MYT1, NEUROD2, NF2, NFE2L2, NHS, NQO2, NOS2, NOTCH1, NPAS2, NPPA, NPTX2, NPY2R, NPY5R, NRAS, NT5E, MYH9, MVD, PTPRZ1, RNR2, LIPA, LPA, LSAMP, MAOB, MAP6, MEN1, MMP2, MMP12, MPI, MPO, MST1, MT3, MTHFR, ND2, ND6, NTRK3, OAS3, OAT, TBC1D25, PMM2, PNN, PPARG, PREP, MAPK1, MAP2K5, PSPN, PRODH, PSEN1, PSMB6, PSMB8, PYY, PSPH, PTK7, PTPN1, PLXNA2, PLTP, PITX2, PC, OCA2, OPRK1, P2RX4, P4HB, PAWR, PBX1, SERPINA5, VIT, PCYT1A, PDE2A, PDE4A, PEG3, PENK, PER1, RIEG2
- Paratyphoid Fever Wikipedia
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Abortion In The District Of Columbia
Wikipedia
American Economic Journal: Applied Economics . 3 : 189–223. doi : 10.1257/app.3.1.189 . Abortion in the United States by state States Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming Federal district Washington, D.C.
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Abortion In Virginia
Wikipedia
American Economic Journal: Applied Economics . 3 : 189–223. doi : 10.1257/app.3.1.189 . ^ Blanchard, Dallas A. (1993).
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Abortion In Idaho
Wikipedia
American Economic Journal: Applied Economics . 3 : 189–223. doi : 10.1257/app.3.1.189 . Abortion in the United States by state States Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming Federal district Washington, D.C.
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Abortion In Oregon
Wikipedia
American Economic Journal: Applied Economics . 3 : 189–223. doi : 10.1257/app.3.1.189 . Abortion in the United States by state States Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming Federal district Washington, D.C.
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Familial Mediterranean Fever
Wikipedia
GeneReview/NIH/UW entry on Familial Mediterranean Fever Familial Mediterranean Fever (FMF) - US National Institute of Arthritis and Musculoskeletal and Skin Diseases Classification D ICD - 10 : E85.0 ICD - 9-CM : 277.31 OMIM : 249100 608107 MeSH : D010505 DiseasesDB : 9836 External resources MedlinePlus : 000363 eMedicine : med/1410 Patient UK : Familial Mediterranean fever GeneReviews : Familial Mediterranean Fever Orphanet : 342 v t e Amyloidosis Common amyloid forming proteins AA ATTR Aβ2M AL Aβ / APP AIAPP ACal APro AANF ACys ABri Systemic amyloidosis AL amyloidosis AA amyloidosis Aβ2M/Haemodialysis-associated AGel/Finnish type AA/Familial Mediterranean fever ATTR/Transthyretin-related hereditary Organ-limited amyloidosis Heart AANF/Isolated atrial Brain Familial amyloid neuropathy ACys+ABri/Cerebral amyloid angiopathy Aβ/Alzheimer's disease Kidney AApoA1+AFib+ALys/Familial renal Skin Primary cutaneous amyloidosis Amyloid purpura Endocrine Thyroid ACal/Medullary thyroid cancer Pituitary APro/Prolactinoma Pancreas AIAPP/Insulinoma AIAPP/Diabetes mellitus type 2MEFV, NLRP3, SEC23B, CRP, TNF, SAA1, CASP1, IL1A, IL1B, TNFRSF1A, ABCB1, IL6, IL1RN, TLR2, SAA2, S100A12, SERPINE1, IL4, IL18, TLR4, KIR3DL2, LEP, LYZ, KIR2DS1, CXCL8, MVK, NM, HBA1, TRIM21, VDR, VEGFA, PSTPIP1, TBC1D9, PYCARD, ADA2, KIDINS220, NOD2, HBA2, MICA, ELF4, CTLA4, FCGR1A, C5AR1, C5, ACE, GRAP2, RNF19A, STS, AHSA1, SIVA1, SERPING1, TRIM38, LPIN2, GLO1, ADIPOQ, ERAL1, AIMP2, CAMP, TNFRSF1B, CASP3, TNFAIP3, CASP8, CD1A, CD1C, POLDIP2, ABCC6, C5AR2, TRBJ2-7, KIR2DS2, MIR204, STING1, AHSG, PRRT2, NLRP12, TRIM5, GSDMD, CARD14, APCS, IGAN1, XIAP, AICDA, RNPC3, PACC1, DDIT4, FASLG, FOXP3, CD14, THBD, CHIT1, SCN8A, GPX1, CRK, LMX1B, LGALS3, MAPK14, KIR3DL1, CYP3A4, JAK2, IL10, CXCR2, IL6R, ESR1, F5, FOS, GEM, IFNA2, HLA-G, HLA-C, GJB2, GLA, CPB2, MIF, AFP, PKN1, CISH, S100B, COL9A1, S100A1, RAC1, PRNP, MAPK7, MAPK1, PRKCB, COMP, PRKCA, PON1, PLG, PIK3CG, COL9A2, COL9A3, TNFRSF11B, OCA2, ABO
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Phenylketonuria (Pku)
Mayo_clinic
Food diaries, computer programs and smartphone apps are available that list the amount of phenylalanine in baby foods, solid foods, PKU formulas, and common baking and cooking ingredients.PAH, QDPR, G6PD, CAT, HNF1A, NEFH, PTS, LRIT1, SHCBP1, PAM, PRDM6, CACNA1A, PELI1, TTR, DMD, LAT, SPR, GCH1, MBP, SLC7A5, TH, GRAP2, SART3, BEST1, AIMP2, OLFM1, TBX1, SOD1, FARP2, PART1, AHSA1, SDS, TPX2, SLC3A2, RNF19A, MMACHC, POLDIP2, SND1, SLC38A7, NIF3L1, ASCC2, COL25A1, NAGS, SLC6A19, MCCD1, SLC22A5, ACADM, PMEL, SAA1, GRM5, GFAP, GCHFR, FN1, NQO1, DECR1, CUX1, MAPK14, CRP, CRK, CNP, CGA, ATR, ASS1, APP, HBB, MAOB, NBN, PGM1, RET, REN, ALB, PTH, MAPK1, POLG, PCNA, NFKB2, PCBD1, PAEP, OXCT1, OTC, OAS3, NME1, NCF1
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Genetic Prion Disease
Gene_reviews
Disorders Potentially Associated with Rapid Progression of Interest in the Differential Diagnosis of Genetic Prior Disease View in own window Etiology Disorder/Comment Gene(s) Hereditary neurodegenerative disorders CSF1R -related adult-onset leukoencephalopathy w/axonal spheroids & pigmented glia CSF1R Dementia w/Lewy bodies (OMIM 127750) GBA SNCA SNCB Familial Alzheimer disease (See Alzheimer Disease Overview. 1 ) APP PSEN1 PSEN2 Frontotemporal dementia (e.g., ALS/FTD, CHMP2B -FTD, GRN -FTD, IBMPFD) C9orf72 2 CHMP2B FUS GRN HNRNPA1 HNRNPA2B1 TARDBP 3 VCP Hereditary ataxia (e.g., SCA1, SCA2, SCA3, SCA6, SCA7, SCA8) 4 ATXN1 ATXN2 ATXN3 ATXN7 ATXN8 CACNA1A Huntington disease HTT Pick disease (OMIM 172700) MAPT PSEN1 Progressive supranuclear palsy (OMIM 601104) MAPT Autoimmune e.g., Hashimoto thyroiditis w/related encephalopathy, multiple sclerosis, antibody-mediated dementia/encephalopathy, CNS lupus, acute disseminated encephalomyelitis Iatrogenic e.g., medication toxicity (e.g., lithium, methotrexate, chemotherapy), illicit drug use Infectious e.g., viral encephalitis (incl herpes simplex virus), HIV dementia, progressive multifocal leukoencephalopathy Metastases/ Neoplasm related e.g., paraneoplastic diseases-limbic encephalopathy, metastases to CNS, primary CNS lymphoma Systemic/Seizures/ Structural e.g., sarcoidosis, epilepsy, nonconvulsive status epilepticus Toxic-metabolic e.g., heavy metals (incl bismuth), electrolyte disturbances (sodium, calcium, magnesium, phosphorus), endocrine abnormalities (thyroid, parathyroid, adrenal), extrapontine myelinolysis Vascular/Ischemia e.g., multi-infarct, thalamic or callosum infarcts, cerebral amyloid angiopathy Adapted from Geschwind [2016], Table 7-4: Partial Differential Diagnosis for Rapidly Progressive Dementias by Etiologic Category ALS = amyotrophic lateral sclerosis; CNS = central nervous system; FTD = frontotemporal dementia; HIV = human immunodeficiency virus; IBMPFD = inclusion body myopathy associated with Paget disease of bone and/or frontotemporal dementia 1.
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Abortion In Kansas
Wikipedia
American Economic Journal: Applied Economics . 3 : 189–223. doi : 10.1257/app.3.1.189 . ^ a b Baird-Windle, Patricia & Bader, Eleanor J., (2001), Targets of Hatred: Anti-Abortion Terrorism , New York, St.
- Dental Fear Wikipedia
- Alcohol Consumption By Youth In The United States Wikipedia
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Abortion In Nevada
Wikipedia
American Economic Journal: Applied Economics . 3 : 189–223. doi : 10.1257/app.3.1.189 . Abortion in the United States by state States Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming Federal district Washington, D.C.
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Abortion In Michigan
Wikipedia
American Economic Journal: Applied Economics . 3 : 189–223. doi : 10.1257/app.3.1.189 . ^ " Man Crashes Into Davenport Health Clinic Archived 2010-03-11 at the Wayback Machine ".
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Mild Cognitive Impairment
Wikipedia
Not to be confused with minimal brain dysfunction . Mild cognitive impairment Other names Incipient dementia, isolated memory impairment Specialty Neurology Symptoms Can include memory impairments (amnestic) or cognitive problems like impaired decision making, language, or visuospatial skills (non-amnestic) Usual onset Typically appears in adults 65 or older Types Amnestic, non-amnestic Risk factors Age, family history, cardiovascular disease Diagnostic method Based on symptoms assessed by a clinical neuropsychologist through observations, neuroimaging, and blood tests Mild cognitive impairment ( MCI ) is a neurocognitive disorder which involves cognitive impairments beyond those expected based on an individual's age and education but which are not significant enough to interfere with instrumental activities of daily living . [1] MCI may occur as a transitional stage between normal aging and dementia , especially Alzheimer's disease . [2] It includes both memory and non-memory impairments. [3] Mild cognitive impairment has been relisted as mild neurocognitive disorder in DSM-5 , and in ICD-11 . [4] The cause of the disorder remains unclear, as well as its prevention and treatment. Contents 1 Classification 2 Causes 3 Diagnosis 3.1 Neuropathology 4 Treatment 5 Outlook 6 Prevalence 7 See also 8 References 9 External links Classification [ edit ] MCI can present with a variety of symptoms, but is divided generally into two types. [5] Amnestic MCI (aMCI) is mild cognitive impairment with memory loss as the predominant symptom; aMCI is frequently seen as a prodromal stage of Alzheimer's disease . [5] [3] [6] Studies suggest that these individuals tend to progress to probable Alzheimer's disease at a rate of approximately 10% to 15% per year. [ needs update ] [7] Nonamnestic MCI (naMCI) is mild cognitive impairment in which impairments in domains other than memory (for example, language, visuospatial, executive) are more prominent. [5] [8] It may be further divided as nonamnestic single- or multiple-domain MCI, and these individuals are believed to be more likely to convert to other dementias (for example, dementia with Lewy bodies ). [9] Causes [ edit ] This article needs to be updated . Please update this article to reflect recent events or newly available information. ( March 2020 ) According to some experts, mild cognitive impairment (MCI) may be caused due to alteration in the brain triggered during early stages of Alzheimer’s disease or other forms of dementia. [10] However, exact causes of MCI are still unknown. Risk factors of both dementia and MCI are considered to be the same. They are ageing, genetic (heredity) cause of Alzheimer’s or other dementia, and risk of cardiovascular disease. [11] Individuals with MCI have increased oxidative damage in their nuclear and mitochondrial brain DNA . [12] A widely studied biomarker of DNA damage, 8-hydroxyguanine was found to be elevated in nuclear DNA of the frontal and temporal lobe of individuals with MCI and in mitochondrial DNA of the temporal lobe compared with age matched control subjects. [12] Other oxidized DNA bases were also increased in the brains of individuals with MCI. These findings suggested that oxidative damage to DNA occurs in the earliest detectable phase of Alzheimer’s disease and thus may play a significant role in the pathogenesis of this disease. [12] Diagnosis [ edit ] The diagnosis of MCI requires considerable clinical judgement , [7] and as such a comprehensive clinical assessment including clinical observation, neuroimaging , [13] blood tests and neuropsychological testing are best in order to rule out an alternate diagnosis.APP, CLU, PICALM, CACNA1C, SORL1, BIN1, NECTIN2, CR1, TAFA2, SNCA, PSEN1, APOE, MAPT, PRNP, TOMM40, EEF1A2, ACTB, SYNJ1, CSF1R, CACNA1A, TBK1, HTRA1, MECP2, C19orf12, ARSA, SCN1A, VPS13C, CSTB, NAGLU, SPG11, PLA2G6, SQSTM1, SLC1A2, TBP, KCNB1, LAMC2, IRF2BPL, FGF12, ARV1, CYFIP2, TBC1D24, BSCL2, NECAP1, PARS2, TRNK, KCNA2, GABRB2, GABRA4, GNAS, PDE11A, IL6, GABRB3, GABRG2, MYORG, ACTL6B, PRDM8, WWOX, ADA2, DARS2, GDAP2, TRNT, GRIN2D, TRAK1, NDUFAF3, NBN, ATXN7, SCN3A, SCN8A, SCN9A, SLC6A1, SLC20A2, SCO2, STXBP1, AP5Z1, SURF1, TEK, TTPA, UBTF, XPA, YWHAG, AP3B2, SGPL1, RPS6KA3, CPLX1, PDE10A, PDGFRB, NDUFB8, NDUFS2, NRAS, NTRK2, SZT2, CUX2, PDGFB, ERCC2, PSAP, CNKSR2, POLG, TREX1, PPP3CA, PRKAR1A, PRKCG, MAPK10, ERCC6, KCNC1, SYNGAP1, HCN1, ACE, CTC1, CLN8, SNORD118, CSF2, COASY, NUS1, CACNA1B, ATP6V1A, MFSD8, SLC13A5, CTNND2, CTSD, BDNF, MCIDAS, CLTC, ABCD1, SLCO6A1, SCN1A-AS1, TIMM8A, DHDDS, CRP, FA2H, ATP1A2, AARS1, UBA5, CHD2, BCHE, DCAF17, ANXA1, ACHE, ATP1A3, DNMT1, DNM1, DEGS2, NGF, ESR1, BACE1, NFE2L2, SERPINA3, NRGN, COMT, ADIPOQ, KL, HTT, MTHFR, DPP4, NOTCH3, NEFL, REN, CD33, PPARG, SIRT1, VEGFA, FMR1, GABPA, GBA, AGPS, IGF1, IGFBP5, DTNBP1, CHRNA4, FGF21, TNF, ALB, PSEN2, CYP46A1, CREB1, GSK3B, PER3, DNM1L, CETP, ABCA7, PINK1, INSR, CCL2, EGF, SMUG1, ADM, C9orf72, ANP32A, WWC1, DENR, ATP13A2, ADAM10, SLC6A3, GDF15, VSNL1, VDR, APOA1, SNAP25, SHBG, SELP, CCL11, SNCG, APOC3, SCD, S100B, SOD1, SPAST, ALDH2, SYP, MIR146A, UTRN, SNCB, EPO, CAT, CRMP1, MMP9, HSD11B1, MEF2C, HSPB2, IAPP, TREM2, LEP, LCN2, RMC1, HMGB1, KCNQ2, IDUA, IL1A, IL1B, ITPK1, IL10, TARDBP, IRS1, HMOX1, IL18, GIP, EGR1, DAPK2, GRN, DNMT3A, GRIA1, EFTUD2, HOOK1, SELENBP1, CREST2, MIR30B, HDAC6, TWNK, BARHL1, SHANK3, CLN6, MIR206, AARS2, NME8, MIR18A, HDAC3, PQBP1, NAMPT, MIR34A, FLAD1, POTEKP, TMEM106B, CCHCR1, SRSF11, POTEM, TRPM7, NRXN3, BDNF-AS, RNF216, GRAP2, SLC16A3, CEBPZ, AKAP6, TREM1, PTGES, CLOCK, SLC16A4, PRC1, HDAC9, C20orf181, NANS, FHL5, TANGO2, ABI3, FIS1, WIF1, POLDIP2, NEIL2, NLRP3, STH, LRG1, PARK7, LRRK2, ACOT7, COPZ1, PLB1, BPIFA2, DKK1, SMG1, ARC, ASTN2, MCF2L, RNF19A, QPCT, FBXO7, IL31RA, CPO, NIPA1, SIRT3, SRRM2, FBXW8, WDR45, SLC17A5, RAPGEF3, TSHZ1, CALCOCO2, UBQLN2, WDR20, MIR106A, SUCLA2, SCGB1D4, IGLON5, DNMT3L, RIDA, RTL1, SPON1, RAPGEF4, AHSA1, CELF1, MTDH, OGA, REM1, HCAR1, SFXN1, PPARGC1A, MMP24, RNU1-1, ACTBL2, MPZL2, A2M, SUCLG2, EP300, GFAP, GDNF, MSTN, GBAP1, MTOR, FLT1, VEGFD, FANCD2, ENO2, LMNB1, EEF1A1, TOR1A, DUSP1, DBP, CYP19A1, CYP2D6, CYC1, CYBB, GHR, GJA1, GLP1R, GNG4, KCNJ13, ITGAM, IRF1, INPP5D, CXCL10, IL6R, IL1RAP, IGFALS, IFNG, IFNB1, IDE, ICAM1, HSPA4, HOXD13, HDAC2, HCRT, GRM5, CTNNB1, CST3, MAPK14, BCL2A1, B2M, AQP4, FAS, KLK3, APOB, AIRE, APBB1, APBA2, ANGPT2, ANGPT1, ALOX15, AKT1, GRK2, ADCYAP1, ADAR, ACTG2, ACTG1, BCL2, BRCA2, CRK, C3, COL17A1, CLN5, CLN3, TPP1, AKR1C4, CHAT, CDR1, CDKN2A, CBS, RUNX1T1, RUNX2, CASP6, CALR, CALCA, CALB1, VPS51, C3AR1, KNG1, LPL, FADD, SETMAR, TRIM21, SRPK2, SOAT1, SLC18A3, SLC10A1, SLC6A9, SGSH, SGCA, ATXN8OS, LRP2, TSPAN31, RENBP, REG1A, RBP4, RAPSN, RAB27A, PTX3, PTGS2, STXBP3, CNTN2, TFPI, TGFB1, TNFSF10, IRS2, UNC5C, ENC1, SRPX, AIMP2, YWHAZ, WNT5A, TRPV1, VGF, TYR, TTR, TPO, TNFRSF1A, TM7SF2, TLR4, TLR2, PTH, PTBP1, PSPH, NTF3, PNP, NOS3, NQO2, NFATC2, MX1, MUTYH, MUSK, TRNW, RNR2, MTR, COX2, MSMB, MPO, MMP13, MIF, MGAT1, MBL2, NPPA, NTRK1, PSG5, NTS, PSPN, EIF2AK2, MAPK1, PTPA, PPARA, PNN, PLXNB1, PLD1, PLA2G1B, PIK3CG, PIK3CD, PIK3CB, PIK3CA, SLC26A4, ENPP2, PAEP, P4HB, STIN2-VNTR
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Spinocerebellar Ataxia Type 17
Gene_reviews
Early-onset familial Alzheimer disease APP PSEN1 PSEN2 AD Dementia No movement disorders Familial frontotemporal dementia w/parkinsonism-17 (FTDP-17) (OMIM 600274) MAPT AD Late onset; progressive movement disorders, dementia, behavior changes; psychiatric disturbances No chorea AD = autosomal dominant; AR = autosomal recessive; CK = creatine kinase; DiffDx = differential diagnosis; MOI = mode of inheritance; XL = X-linked 1.
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Csf1r-Related Adult-Onset Leukoencephalopathy With Axonal Spheroids And Pigmented Glia
Gene_reviews
Disorders to Consider in the Differential Diagnosis of CSF1R -Related Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) View in own window Disorder Gene(s) Clinical Features of This Disorder Overlapping w/ CSF1R -Related ALSP Distinguishing from CSF1R -Related ALSP Autosomal dominant disorders Alexander disease GFAP Bulbar/pseudobulbar signs, ataxia, spasticity Palatal myoclonus; cognitive function in adults frequently normal; infratentorial atrophy on MRI Adult-onset autosomal dominant leukodystrophy (OMIM 169500) LMNB1 Cognitive impairment, pyramidal & cerebellar signs Early autonomic dysfunction; a periventricular normal rim on MRI CADASIL NOTCH3 Frontal lobe syndrome, WML Stroke-like clinical signs; multiple cerebral infarcts & WML incl the characteristic temporal pools MAPT -related disorders (OMIM 157140) MAPT Progresses over a few years into profound dementia w/mutism Frontal &/or temporal atrophy w/far fewer WML Frontotemporal dementia, chromosome 3-linked CHMP2B Frontal lobe affected; pyramidal &/or extrapyramidal signs Frontal &/or temporal atrophy w/far fewer WML GRN -related frontotemporal dementia GRN Frontal lobe affected; pyramidal/extrapyramidal signs Frontal &/or temporal atrophy w/far fewer WML C9orf72 -related FTD C9orf72 Frontal lobe affected; pyramidal/extrapyramidal signs Frontal &/or temporal atrophy w/far fewer WML Early-onset Alzheimer disease APP , PSEN1 , PSEN2 Executive dysfunction & personality changes; similar onset age Episodic memory loss; WM changes present but much less pronounced Autosomal recessive disorders PLOSL (Nasu-Hakola disease) TREM2 , TYROBP Insidious personality changes, frontal lobe syndrome, motor impairments, dementia & progression to vegetative stage Pain/tenderness of feet/wrists, polycystic osseous lesions, pathologic fractures; U-fibers partially affected Vanishing white matter EIF2B1 , EIF2B2 , EIF2B3 , EIF2B4 , EIF2B5 Cognitive decline, spastic paraparesis, cerebellar ataxia Stress-induced deterioration w/minor trauma or infections; more widespread & diffuse WM changes & atrophy than in ALSP; cystic breakdown of the WM Adult type of metachromatic leukodystrophy ARSA Executive dysfunction, personality changes, memory problems, pyramidal signs and seizures Peripheral neuropathy; spread of WML into the cerebellar region & WM myelin breakdown w/low-density tigroid stripes Adult form of Krabbe disease GALC Pyramidal signs, developing into para- or tetraparesis Peripheral neuropathy; MRI w/predominance in the posterior part of the WM.