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Glioma Susceptibility 4
Omim
No evidence of involvement of known tumor syndromes was obtained from the data provided by the linkage analysis or hospital records.TP53, IDH1, CDKN2B, PTEN, NBN, SPP1, BRAF, ATM, CDKN2A, NF1, HRAS, RTEL1, CCDC26, ACVR1, EGFR, PHLDB1, MGMT, MDM2, GDNF, ATRX, PTGS2, BMI1, TNFSF10, CHI3L1, XRCC1, H3-3A, TNF, ERBB2, FGF2, PIK3CA, TERT, GSTP1, SLC5A5, ROS1, RAF1, PLK1, HLA-C, FBXW7, STMN1, TOP2A, POT1, TFRC, KLF6, CLCN3, MDK, FGFR1, NTRK1, CIC, SOD1, CAT, XBP1, HLA-A, HLA-B, MYB, PPM1D, ATP1B2, FUBP1, APC, CDKN2C, MSH2, PIK3R1, ALK, HMGN5, H3C2, NTRK3, DMBT1, APOD, CLCN2, FTH1, ATR, PMS2, SUZ12, QKI, GJA1, DMXL1, PSD3, IFNG, NTRK2, CCR4, MET, IL12A, IL12B, FAM107A, XAF1, BRCA2, MYLK, MYBL1, CTSB, STAG2, TNC, MMP2, TRIM29, CLCN5, BCAN, AKT2, BIRC5, HMGB1, ANGPT2, CAV1, SPHK1, BAD, EPOR, SIRT2, CSF1, CXCR3, LGALS3, MKI67, CD80, ST6GAL1, YEATS4, IL7, AREG, F2, SH3GL1, SLC6A3, MDM4, CAV2, ATG7, PCMT1, BDKRB2, LRIG1, CDKN2B-AS1, RAB27A, ETFA, VTI1A, CHEK2, STN1, AKAP6, AKT3, STK38L, SMYD3, TREH, MAML2, GLI3, C2orf80, SLC16A8, HIF1A, GDE1, ZBTB16, EPHB2, LRP5, ABCB1, MALAT1, ERCC1, ERCC2, CXCR4, IDH2, DBT, HGF, PDGFRA, CD44, TRAF5, NRP1, NFE2L2, EZH2, PIK3CB, MTDH, PIK3CD, SERPINE1, EGF, OLIG2, MIR155, SLC25A24, TNFRSF12A, VEGFA, E2F1, MMP9, PLAU, MIR145, POLR2A, MIR21, ACOT11, PKM, MAPK14, DNMT1, XRCC3, GSC, CD274, YAP1, PIK3CG, POU5F1, MIR221, PCNA, CDK4, CDK2, CTNNB1, MCL1, NOTCH1, HPGDS, MIR182, GOLGA3, MAPK1, BDNF, TBC1D9, SPARC, MTOR, KDR, LGI1, FAS, AQP4, COX2, IL13RA2, STAT3, IL13, IL10, MIR34A, POU5F1P3, CXCL8, MYC, RAC1, IL6, CCND1, BCL2, FOXM1, SOX9, HEATR3, SOX2, RTEL1-TNFRSF6B, H3P10, MEG3, MMP14, LOC110806263, ACTB, MTCO2P12, RNU6-1318P, CXCL12, MIR4300HG, GLI1, HOTAIR, POLR3B, RAVER2, PARP1, SHANK2, ABCG2, GFAP, ABCC1, AKT1, KIF26B, GOLPH3, POU5F1P4, TGFB2, CASP3, TSPO, PTN, PTK2, NES, TGFB1, IL4R, LMF1, LRRC31, IGFBP2, H3-3B, CASP8, SLC35A3, DKK3, MAP2K7, CCK, IGF1, PPP1R2C, PROM1, IFNB1, F3, MAPK8, MAPK3, IL1B, NEAT1, PVT1, IL4, RHBDF1, ZEB1, IL2, SIRT1, LRRC4, MIR107, COMMD3-BMI1, IL24, CSF2, HMGA2, VIM, BAX, MIR126, NFKB1, CRK, MIR205, CDK6, MIR146B, CDKN1A, MIR200B, HSPB1, CDKN1B, EPHA2, GSTT1, RNF19A, HOXA11-AS, EFEMP1, LGALS1, CCL2, POLDIP2, PDGFA, TICAM2, AIMP2, PDGFRB, AHSA1, MIR203A, HSPA5, UCA1, CRNDE, NOTCH2, MIR139, GABPA, MIR10B, TMED7, PPARG, FASLG, SETD2, SALL4, PAX3, PSMD9, GRAP2, JAG1, PTPN11, TMED7-TICAM2, FLT1, FN1, COL18A1, BECN1, CASC2, FOXO1, NGF, FGFR3, GLB1, FOXO3, HSPB3, SLCO6A1, SDC1, IGF2, S100B, CASP9, MIR200A, HSPB2, HPSE, MIR137, TWIST1, SMUG1, MIR132, ROCK1, MIR29A, POSTN, IFI27, CTSL, MIR130B, PDPN, DCTN6, ATF5, GSTK1, ZNRD2, THBS1, H3P23, CCN1, IL1A, TIGAR, PTTG1, XRCC6P5, MIR195, MIR184, XIAP, MIR183, ZEB2, VDR, IGF1R, TLR9, STAT1, FOXD2-AS1, PRKCA, TIMP2, CDC42, GAS5, TCF4, CYTOR, BMP4, TEK, BSG, ING4, AURKB, SP1, PDGFB, MIR106A, PBK, ACKR3, HSPA4, FZD7, MIR140, SLIT2, WNT5A, CREB1, MIR122, MIR15B, SMAD2, KLF4, ANXA5, PECAM1, MIR675, MIR451A, TF, TLR4, MSH6, GORASP1, MIR338, ITGAV, GDF15, PTBP1, FGF13, NCL, GLI2, TGM2, PTPRZ1, WNK1, MIR342, KLRK1, HDAC6, KLRC4-KLRK1, SNAI1, SLC2A1, GAS1, KMT2A, ILK, TP73-AS1, RELA, SRPK1, CD163, LILRB1, AQP1, MTHFR, NLGN3, LRIG2, AHR, CXCL10, SYT1, ADAM17, DICER1, AXL, MIR497, ALB, TAZ, MSH3, GLIPR1, FOXP1, CCNE1, WLS, MIR20A, WWTR1, EGR1, MIR185, MIR186, SPINT2, MIR19A, KHDRBS1, MIR23B, MIR204, MIR210, MIR214, MIR222, HAVCR2, BEX2, PLG, OSM, FOXP3, NDRG1, PRDX1, MIR142, MIR141, DSC3, VCAN, XRCC4, LDHA, ZEB1-AS1, ZFP36, PGAM1, PEG3, DCN, TFPI2, ICAM1, MIR146A, CD34, PRKAA2, HDGF, MIR98, MIR320A, PRKDC, NOS2, BCL2L12, ETS1, MIR30A, PRKCB, FABP7, ERCC4, NGFR, MIR93, EPO, PTK2B, CDK1, SEPTIN7, MIR326, PRKAA1, LRP1, ITGA3, RASSF1, HDAC1, PRMT5, PSIP1, SND1, CXCR6, JAK2, ITGB1, H2AX, ITGA5, MMP3, NOB1, ZHX2, UBD, TACC3, MFAP1, MARCKS, ABCB6, SIRT6, SNHG1, PPP1R13L, KNG1, GAB2, KRAS, MECP2, HLA-DRB1, TRIM28, BRD4, HDAC4, EGFL7, IFNA1, ANGPTL2, WWOX, IFNA13, G0S2, HSP90AA1, IL17A, RECK, CUX1, RB1, DACH1, MIR424, DCX, TERC, TIMM8A, DHCR24, PDCD1, PVR, PCBP2, PBX3, PAX6, TCF7L2, PDIK1L, TCF3, E2F3, ECT2, LGR5, RAD51, TAC1, LINC00461, SLC22A18, TRAF6, PRRT2, MIR584, ABCC3, TGFA, MIR377, MIR106B, TLR2, PRKAB1, CDC25A, MIR27A, PRKCI, MIR23A, ZFAS1, MIR215, MIR211, VHL, MIR133B, CLDN5, TIMP1, MIR375, MIR152, MIR149, XIST, MIR136, MIR134, MIR125A, MIR373, CCN2, CTLA4, MIR10A, CX3CR1, RIPK1, CD70, SHH, SATB1, S100A4, NFATC2, SOAT1, DHDDS, SLC12A9, ROBO1, SNHG16, MSC, AICDA, SMARCA4, NEDD4, MARCKSL1, CPEB1, SNAI2, FRK, FOXD1, NDRG2, FLT3LG, FOLH1, CHPT1, S100A1, SESN2, FADD, AJAP1, EPAS1, SST, APRT, ESR2, ASIC2, MIR92B, NOTCH3, ADAM9, TNFRSF10B, MAGED4, APEX1, ESR1, CCL5, SDCBP, THY1, S100A9, TP73, RPSA, SFRP1, TNFRSF1B, ITSN1, STAT5B, PTHLH, SIX1, RALBP1, RBL2, KIT, STAT6, STK11, TAT, CNTN2, UPF1, RFX1, L1CAM, RSU1, FSCN1, TFAM, TFAP2A, PTPN1, UBE2C, TRIM31, SSTR4, TGFBI, AURKA, IKBKE, TTC4, IL18R1, NEK2, PER2, NF2, HDAC3, IQGAP1, CD46, PTPRU, TNFRSF4, TNFRSF10C, NOS1, ACTR2, NAMPT, EBI3, NRAS, NEFL, NELL1, NEDD9, SQSTM1, MYH2, BCL10, PDCD5, MTAP, MELK, MLH1, HDAC9, COX5A, MMP1, MSI1, MRC1, KIF23, CLOCK, YBX1, MAP2, PSMG1, SERPINF1, TXN, EZR, LCN2, PLP2, TRPV1, VWF, WNT1, WT1, IGF2BP3, MMP7, LIF, LIG4, BTG2, CDK14, LOX, MAOB, FOSL1, CIB1, PDK1, SLC7A5, MCRS1, AXIN2, BRAP, SERPINA3, SEMA3A, SMAD4, PAK4, P2RX7, SPRY2, KHSRP, WIF1, FOXA1, BNIP3, FAT1, PDXP, BTK, DANCR, FPR1, MIR429, MIR423, MARK4, MIR383, MIR382, MIR381, MIR378A, MIR374A, FOS, CALR, NGB, MIIP, FOXC1, ADGRL4, FGFR2, CAPG, MIR335, RUNX2, RUNX1, KLF9, GAPDH, BRCA1, LARP6, ROBO4, GRM3, ASL, ATP1A1, TET2, NR3C1, TRPM7, TUG1, CEP55, MIR504, TNFRSF19, SLC2A4RG, MIR524, MIR181D, MIR494, MIR491, MIR490, GLS, MIR489, MIR485, MIR410, GBP1, NANOG, SERPINH1, GSK3B, TET1, RBM45, E2F2, DUSP2, MIR15A, MIR150, ATN1, DPP4, MIR148A, COX8A, CPE, CPOX, DOCK1, FOXK1, CRP, CSF1R, MIR130A, TINCR, LINC00174, CYP1A1, MIRLET7B, CYP2B6, IRGM, LINC01194, MIR188, MIR200C, CFL1, CD151, MIR324, CPEB4, CD276, MAGED4B, CCND2, ERN1, MIR31, ERBB3, EPHB4, CD68, CTTN, CEBPB, WNT3A, MIR26B, PYGO2, CDH1, MIR224, MIR223, ELAVL1, MIR219A1, CEACAM5, MIR206, SNHG20, CYP19A1, GSTM1, IL2RB, DCTN4, TNFRSF9, SASH1, ADCYAP1R1, IL13RA1, ANXA2, CCL22, ANGPT1, OCLN, IL22, NOP53, SIRT3, MIR216B, EEF2K, IKBKB, MIR661, RGCC, DLL1, PDCD4, AGO2, SIGLEC7, IGFBP6, CBX7, HP, SNHG18, NUP62, GSTM3, SLC7A11, HSPA1B, HES1, ING1, HSPA1A, SPRY4-IT1, HK2, GTF2H1, MMRN1, ISG20, ADAM22, RND3, ADA2, DKK1, MIR599, MIR613, MIR622, NRG1, HCLS1, PTCSC3, GACAT3, UGT1A, UBE2N, SKP2, WNT7B, TYMS, SHMT2, XPO1, YY1, CCAT1, MIR25, ZAP70, SDC2, ZFX, HOTTIP, MIR1908, MIR1301, TRPC6, TRPC1, MIR27B, BCAR4, MICA, MIR296, TRP-AGG2-6, UCN, WNT7A, MIR17, MIR127, MIR301A, WSPAR, MIR16-1, XRCC5, MIR181A2, PANTR1, GHET1, MIR181C, MIR129-2, MIR193A, SIM2, UGT8, BLACAT1, VEGFC, LINC02605, HOTAIRM1, SH3GL2, H3P5, USP1, UQCRFS1, LINC00958, MIR143, MIR18A, SLC22A3, MIR30B, SOX4, MIR638, TEP1, MIR650, SNHG5, OIP5-AS1, MIR452, ACOD1, MIR433, MIR363, MIR449A, MIR454, NR2F2, MIR770, SOX10, MIR448, MIR376B, MIR637, TRA, STC1, SYP, SUV39H1, SULT2A1, SNHG6, MIR539, MIR421, HAS2-AS1, TCF12, MIR592, STAT5A, MIR193B, MIR495, MIR634, SSTR2, MIR4435-2HG, MIR384, SLC8A2, MIR876, SMN1, MIR1231, MIR1294, SMARCA1, MIR1236, MIR17HG, MIR96, TPM3, SLC12A2, MIR95, MIR33A, TPT1, MIR32, SLC9A1, MIR30E, SMN2, MIR328, MIR1275, MIR936, SOD3, MIR361, HCG11, MIR374B, TGFBR2, MIR372, THBS2, CD24, MIR367, SNCA, MIR346, MIR940, MIR340, NR2E1, KLF8, AGPS, LINC01116, PIEZO1, DLL4, ELMO1, SV2A, KIF14, MVP, SCO2, PPIL3, HDAC5, FRAT1, CAB39, ACSL5, NLK, SMC4, MPC1, RNF138, KIF20A, HIPK3, TRAP1, TRPV2, ZMYND10, PHF20, KEAP1, FBLIM1, NCR3LG1, RMDN3, ADGRG1, CTNNBIP1, PNO1, SLC9A3R1, RAD18, SPHK2, PANX2, NTN1, POLE4, METTL3, ARHGAP15, NSUN5, URGCP, NLRP2, TMEM59, PTGES, CXCL14, SOX6, CDCA7L, BATF3, ZNF654, NDUFA13, RNF41, MPHOSPH6, ASCC1, SRRM2, DLL3, POLD3, CBX5, KDM5B, MTHFD2, GJB6, SYNM, USP22, FGL2, SUB1, MPRIP, FERMT2, SLC27A3, KDM6B, PEG10, RIPK3, PHLPP2, KDM1A, PTP4A3, CBX3, CADM1, CAMKK2, IL17RA, SEMA3C, F11R, TNIP1, DELEC1, ADGRE2, RACK1, NDC80, IFITM3, TMEM97, RBMS3, CACYBP, IGF2BP1, GREM1, LATS2, MYCBP, PHGDH, TRIM3, NOC2L, PHF19, ARHGEF26, CHD5, PIWIL1, PAK5, MTA2, CREB3L1, FOXR2, CD109, ATRN, LRIG3, PIK3R3, PARK7, VASN, BHLHE40, MIR155HG, DENR, MKNK1, NLRP3, UCN3, AZIN2, EGLN3, TP53INP1, PEA15, FOXQ1, TRADD, MBTPS1, TNFSF12, ULK1, PIWIL4, PWAR1, MAGI3, MACC1, SEMA3B, USP7, GADL1, LINC01139, SNHG15, HOXA-AS2, CAVIN1, ADGRF1, IL27, GLIPR2, CTAG1A, SPDYA, LGI3, SPAAR, MIA, MLRL, LINC00599, LZTR1, RDH10, ATP23, IL33, GATAD2B, ADAM23, IER3, MAPKAP1, P2RY12, ARHGEF7, HHIP, IL21, CXCL16, MBD2, CADM3, POLD4, PKD2L1, SEMA5A, SLC7A7, DIRAS3, NMI, LATS1, INA, AIFM1, ANKRD36B, MIB1, LPAR2, MMP28, SLC52A2, SHCBP1, BRMS1L, DIXDC1, CD164, TSPYL5, TNFRSF11A, SNHG12, ORAI1, TNFRSF10D, MAK16, ECRG4, TNFRSF10A, FER1L4, TRIM24, HSDL2, MINDY4, ZIC4, NUF2, NRP2, ARHGAP24, TRIM11, NR1I2, NAT2, H3P40, CXCL9, PIN1, PKD2, EMP2, HOXC10, PLAUR, EMP1, RHOA, ARF6, HOXC6, PLD1, MT1JP, HOXB3, PLOD2, ARAF, PLXNB3, CCR5, PITX1, SLC25A3, AQP9, FASN, ENG, HSP90AA2P, HSPA8, HSF1, ACSL4, ATF4, PER1, CDKN1C, ASPA, PFKFB4, PGK1, MUC1, AGFG1, HOXD9, MTRR, CCR6, CNR1, FKBP5, ANXA6, CRYAB, CSF3, CSK, AMBP, CST6, CD200, MAP2K1, ALDH1A3, CTAG1B, CTBP1, PRNP, CTSD, KCNMA1, PROX1, HMOX1, ANXA1, ANXA7, MT1E, HOXA@, CNTFR, POLD1, COL3A1, HOXA9, FEN1, COL4A3, EFNB2, MSN, PPARA, EFNA1, COL11A2, PPIA, KCNA5, FGF1, CP, CDK7, HSPG2, FANCD2, CD2, CALM2, IL2RA, CALM1, CALD1, P4HA1, P4HB, PEBP1, CALCR, NFKBIA, DDR1, PAEP, CA9, CA2, ERCC5, VPS51, CALM3, CAMK2B, HTC2, CCNH, NT5E, IMPA1, EPHA5, NTSR1, NUP98, IDO1, OPA1, RUNX3, NOVA1, IL18, CASP1, CCNG2, IL16, IL15, NME1, RBPJ, IGFBP7, CD86, EPHA3, ADGRE5, BCL2L1, EPHA1, MYCN, CDC20, MYBPH, CDC25C, CDH2, F2R, CDH13, ITGB3, F2RL1, PCDH8, PCDH9, MXI1, BCL3, IRS1, BCL6, KLF5, INSR, NFATC1, IGFBP3, IGFBP1, CD40, BTF3, BRS3, IRF7, CD40LG, IRF3, BMP7, ID2, ETV4, BGN, HMMR, CCNB1, LPL, MGP, CYP17A1, GRIN2B, RASGRF1, MCM2, RARB, ACE, HIC1, DCT, FOSL2, RAP2A, FOSB, RAB27B, ADRA1A, RANBP2, HK1, GRIA1, FLT4, GH1, ACTL6A, ADRA2B, ADRB2, HLA-E, ADM, DUSP4, GALNT2, LAMC2, TRIM27, FUS, ADARB1, REST, LGALS9, MEF2D, GSN, RELB, HAS2, REG1A, G6PD, HELLS, RDX, MEN1, LASP1, GRM1, FOXG1, CFH, XRCC6, DUSP1, HFE, GPX1, FUT4, SMAD3, SCD, MMP12, GPR42, PTX3, PTPRZ2, EDNRA, SAI1, PTPN2, PXN, DNMT3A, GLO1, KIF2A, PTPN3, SMAD7, DECR1, PSMB4, ACAT1, AEBP1, MXD1, TYMP, PSEN1, PSAP, DDX5, CCL20, RAB1A, PSEN2, DVL2, RAB5A, CCL8, GLUD2, AFAP1-AS1, ACRBP, MARCHF8, DIRAS1, EPHA4, DNM1, SNORD35B, RCAN1, DRD5, PCGF1, SLC29A1, DTX3L, PAQR3, DKC1, RMDN2, SPZ1, CCNY, TMEM167A, DNM2, DACT2, ADGRE3, PAQR7, CITED4, ANO6, KDM2B, MLKL, ENO1, PPP1R9B, LGI4, ZNF296, SLFN5, SLC5A8, CADM4, FMR1NB, DNMT3B, TET3, DPEP1, SLC39A11, PAXIP1-AS1, ZGPAT, PRSS55, SLC26A3, LNX1, PEBP4, SGMS2, LINC00689, PLEKHA8, SKA1, AGAP2, SNORD14E, ATG4C, ZFP42, LACTB, EEF1G, EDN1, MCM3AP-AS1, LINC00313, FAM83F, FAM168B, SLC52A3, TMEM18, SLC46A1, DYRK1A, EFNB3, VPS37A, EIF4E, EGLN2, EIF4EBP2, MEGF10, CMPK2, SERPINB1, IKBIP, THEM4, ANTXR2, LRG1, IL22RA2, KIR3DL3, PRAP1, UHRF2, H4-16, PHC1, RAB42, ATG4A, LGMNP1, EDNRB, JDP2, TSACC, CYGB, TMEM71, PASD1, AJUBA, E2F7, EMX2, EN2, ZIC5, RHPN2, SNORD14D, OR2AG1, SNORD14C, HBEGF, MIB2, CEP128, RBM17, DSPP, ATG4D, LINC00052, TTBK2, LINC00526, EMP3, UNC5A, UPRT, NLRP12, ORMDL3, ST7-AS1, DVL1, NAPRT, GAB3, NAF1, ELF4, PCED1B, STARD13, ELK1, ELK4, S100A16, SPOCD1, ZBTB46, LINC00473, DYNLL2, EEF1B2P2, MAP1LC3B, PHYHIPL, FXN, PRDM13, FLNB, KMT2C, NLRC4, ENOPH1, SRPRB, FLNC, FLOT2, PTBP2, FMOD, GATAD1, SCUBE2, KIAA1549, TSHZ3, CFAP97, PCDH10, SEMA6A, FPGS, RPTOR, GPR158, MTA3, FPR2, REXO1, TRPV4, PBOV1, TGIF2, NOD2, FHL3, CDH22, VEGFD, SIL1, ARHGAP9, COP1, NSD1, FBRS, FKBP4, ARHGEF28, TNMD, FLG, SMOC1, SAMSN1, FOXL1, PRSS22, ERVK-6, HEATR6, PIEZO2, FOXC2, PROK2, FOXD2, PLEKHG5, SCYL1, MAP3K21, FTH1P3, LRRC8A, GSDMC, TEX11, PCDHGA11, SLC50A1, GJB2, SULF2, ACSS2, GCLC, GCLM, CENPJ, UBAP2, ADCY10, CACNA2D3, PRR11, AGK, HHAT, WDR11, GLDC, GLP1R, GLUD1, SYBU, CHD7, MMP26, DIABLO, KAT2A, GAB1, TTYH1, GAST, VANGL2, SMURF1, FZD2, RTN4, GOPC, PNPLA2, SLC17A7, SLC37A4, GAD1, GBP3, LHX9, PMEPA1, CA10, SEMA3G, GAP43, LGALS14, GAS6, GATA2, SLAMF8, GATA6, FHL2, TMPRSS3, GPC5, FGF9, DDX59, EXT1, MED25, ST6GALNAC5, SPRY4, NUAK2, NQO1, KAZALD1, TRIM8, NDEL1, EZH1, CLPTM1L, ZNF436, CMIP, F10, PDCD1LG2, ACSL1, ACSL3, SPHKAP, TRIM45, ORAI2, FHOD3, CTC1, MECOM, RASSF5, SOX7, EYA4, CARD11, EPHA8, AKT1S1, EPS8, ING5, BTBD10, RPAIN, EREG, ZDHHC18, USP48, KAT8, ESRRA, PCBD2, USP44, MAGT1, REG4, RASSF4, RAB34, FSD1L, KLF16, FERMT3, JAM3, FBXL18, NAA25, WWC2, RHPN1-AS1, FSD1, BRCC3, FECH, DERL1, CHAC1, TRPM8, AHNAK, GGCT, LINC01260, CUEDC2, DUSP26, BHLHE41, WNK2, FGF4, RTN4R, NBEAL1, CDK15, NDRG4, NT5DC2, BCL11B, NIBAN2, FGF7, IRX1, FDXR, C10orf88, LIN28A, BPTF, FAP, FBP1, GGNBP2, LINC00115, CAMKMT, FCER1A, FCGR1A, GEMIN7, ADGB, SUV39H2, NKAP, RIOX1, CENPU, DYNC2H1, MCPH1, TNFAIP8L2, RNASEH2B, HMBOX1, TCTN1, CHPF, FCGR1B, DIAPH1, CXCL11, DES, MIR300, ANPEP, MIR766, MIR769, MIR767, MIR671, SNHG9, APAF1, LOC730100, NBAT1, BIRC3, NAIPP2, USP17L30, USP17L29, USP17L28, USP17L27, USP17L26, USP17L25, USP17L24, APLP2, LOC728196, LINC00460, MIR663A, APOC2, ANG, AMPD1, AIF1, MIR744, MIR1468, TMEM238L, CASC11, PCED1B-AS1, TPT1-AS1, MFT2, MIR1224, ALAD, HOXA-AS3, RAB6C-AS1, AGAP2-AS1, UBE2CP3, MATN1-AS1, C20orf181, FAM83H-AS1, EGOT, MIR760, MIR543, MIR708, ALDH1A1, AKR1B1, MIR301B, MIR873, MIR656, MIR654, H2AC19, MIG7, ARL2, H3P38, ARL3, ARNTL, SCFV, RAET1K, ART1, ASCL1, MNX1-AS1, RASSF10, MT1IP, FLVCR1-DT, CERNA2, ATIC, POTEM, MIR455, MIR486-1, MIR484, MIR483, LINC00589, ATP1A3, ZFAT-AS1, MIR509-1, MIR487B, MIR542, MIR411, MIR610, APOE, APP, MIR646, AR, ABCC6, MIR630, MIR628, MIR625, MIR616, ARCN1, MIR608, ARHGDIA, MIR605, MIR603, ARL4D, MIR596, MIR593, MIR577, MIR576, MIR564, MIR548C, MIR532, MIR1265, MIR1287, MIR506, LINC01857, MIR6807, MIR6852, MIR6743, MIR6165, LNCNEF, UBE2R2-AS1, LINC01198, ACVR1B, TRPM2-AS, LINC01494, CASC9, ACYP2, LSINCT5, FOXD3-AS1, ADA, LINC-ROR, HOXC13-AS, HOXC-AS2, HOXA10-AS, MIR5582, PCAT1, LINC01023, ADAM10, GATD3B, TP53COR1, MIR1249, CCND2-AS1, H3P29, AAVS1, ABCA1, H3P24, ABCA4, H3P8, H3P9, LNCRNA-ATB, MNS16A, ACP3, PSMD6-AS1, CNE-2, H3P14, ACTC1, MIR3142HG, ACTG1, MDC1-AS1, CST12P, FOXD1-AS1, ACTG2, LINC02210-CRHR1, ACTN4, SNHG14, MIR4725, ERVK-20, MIR4518, MIR4775, MIR210HG, LINC01503, LUCAT1, LINC00645, MAGI2-AS3, CARD8-AS1, MIR3908, LINC00673, MIR4262, MIR3175, MIR4295, MIR3148, MIR2276, FTX, MIR1290, ADSL, MIR1202, AP2A1, MIR1271, MIR1825, AGER, MIR1205, APLNR, ADORA2A, ADORA1, LINC01426, LOC100507703, MIR4493, MIR1587, MIR4500, MIR499B, MIR4731, ADAR, RAB4B-EGLN2, BCL2L2-PABPN1, ADARB2, RBM14-RBM4, PSMB8-AS1, CBR3-AS1, ADCY2, ADCY8, ADAMTS9-AS2, MELTF-AS1, ADCYAP1, TUNAR, PWAR6, HOXD-AS2, ADK, PXN-AS1, MIR508, ATP7A, RICTOR, CYC1, MIR100, MIRLET7G, MIRLET7E, MIRLET7C, CYP1B1, CYP2C9, WDFY3-AS2, HAPLN4, FAM224A, GASAL1, CASC15, HAGLR, LINC00909, LINC00511, CYP2D6, USP17L9P, SLC39A4, FEZF1, CYP2E1, TRABD2B, HES5, KMT5A, LINC00320, CYLD, CTSK, CLK1, CTNND2, CNTF, MIR181B1, CNTN1, COL4A1, COL9A1, COL9A2, COL9A3, MIR154, COMP, COX4I1, COX5B, COX7A2, ATF2, CRH, CRHR1, CRMP1, CRY1, CRY2, CSPG4, CST3, MIR128-1, CTBP2, CTNND1, CYP2J2, CYP4B1, USP17L2, LHFPL3, LINC00319, ZNF326, RSPO1, EMC10, CXCL17, GADD45A, DDIT3, H19, LINC00515, HCA1, DDX6, CYP4X1, ASPM, SGMS1, SVIP, SHPRH, DHX15, PTF1A, SYT14, MCOLN2, TAC4, ZDHHC23, CADM2, STPG4, TUSC7, SLC9A9, DBP, ASPG, CYP27B1, DAG1, PRAC2, DAO, SKA2, SOX2-OT, DAXX, ACTBL2, DBN1, DCC, DCK, RAB43, GPIHBP1, CHSY3, CELIAC2, TRIM59, LIN9, FAM133A, PAXX, SCAI, DLX6-AS1, CCR7, MIR190A, MIR503, BTG1, C1QBP, SAMD12-AS1, SERPING1, DUXAP8, RGMB-AS1, MIR425, PTTG1IP, MIR422A, CA11, MIR379, CALCA, CISD2, MIR196B, CALML3, MIR370, MIR376C, CAMK2G, CAMP, CAPNS1, CASP2, CASP6, MIR330, CBL, BUB1, H4C15, CLIC1, MIR362, MIR501, MIR499A, MIR527, MIR520D, MIR519D, MIR517A, BAG1, MIR520C, MIR520B, MIR520A, ADGRB1, BCAT1, MIR496, BCL2L2, MIR432, MIR202, BDH1, CEACAM1, MIR488, PRDM1, BMPR2, MIR409, ZFP36L1, KRIT1, MIR323A, MIR302C, MIR302B, CDK5, MIR218-2, MIR217, CDK8, MIR212, CDKN2D, CDKN3, CDX2, CEBPA, CEBPD, CHD1, CHD4, CHEK1, CHKA, CISH, CLC, MIR19B1, CLCN4, MIR199A2, MIR199A1, MIR197, MIR196A2, CLCN7, CDH18, CDH11, CDH5, CD28, CCND3, CCNF, LOC441204, POTEKP, MIAT, TNFSF12-TNFSF13, CD247, CD8A, MIR34B, CD27, TNFSF8, CDH4, ENTPD1, CD47, MIR302A, CD48, MIR29C, MIR29B2, MIR29B1, CD74, MIR28, CDC25B, DEPDC1, GUCY1B1, TENT5A, P2RX4, EIF3D, EIF3C, EIF3A, PDE5A, NCOA1, OPRD1, KLF7, PLA2G4C, CASK, OPRK1, OXCT1, CDK10, TAGLN2, P2RY1, FURIN, PCSK6, GPR65, SMARCA5, CUL1, DYRK2, RAD54L, CAVIN2, PAH, SNHG3, EIF3I, VAMP8, TNFRSF11B, OPCML, NFATC3, NFATC4, CFLAR, NFIB, NFIL3, NFIX, CES2, NHS, SUCLG1, NINJ2, NOP2, NPY, DLK1, RIOK3, NOVA2, TNFRSF6B, RIPK2, NPM1, NPPC, NTF3, NTS, ODC1, HYAL2, SERPINB2, SPOP, PER3, TAM, PRKN, BAP1, PAWR, H4C9, TKTL1, SMC1A, USP9X, PCBD1, DVL1P1, BAS, GATD3A, CDR3, SPARCL1, PCSK1, ANP32A, PWAR5, CDK2AP1, CDK16, PDE4C, KMT2D, PDK3, CSRP3, MLLT10, PSCA, CDC45, FZD4, PAM, H2AC18, MAD1L1, HYAL3, H4C14, H4C13, H4C5, H4C2, H4C8, H4C3, H4C11, H4C12, H4C6, H4C4, H4C1, PAK1, H3C10, H3C12, H3C8, H3C11, H3C6, H3C3, H3C4, H3C1, H2AC20, APLN, NEO1, ENOSF1, FHL5, MOV10, GOSR1, LITAF, GAL3ST1, ADAMTS1, MAGED1, MPG, MAPK8IP1, ROCK2, MPI, ARHGEF6, AIM2, NRXN3, GSTO1, MPZ, NCR1, MRE11, MYO1B, ZNF264, DDX23, ZRANB2, RECQL4, TSIX, MSR1, BAG3, MMP16, MMP15, BCAR1, CD99, SPOCK2, CKAP5, PCLAF, MITF, KMT2B, SLK, MME, DCAF1, NOS1AP, HERPUD1, ULK2, UBE3C, KDM4A, PHF14, MDC1, SH3PXD2A, AKAP12, WTAP, APOBEC3B, SOX13, BABAM2, MMP13, ADIPOQ, MST1, SEPTIN2, MYBL2, MMUT, DNAJA3, MUTYH, ANGPTL1, SYT7, MVD, PRC1, MX1, SOCS3, MAP3K14, HAP1, PLOD3, MT1A, WASL, H3C7, BTRC, MBD4, TIMELESS, CCNA1, MTMR3, MYH10, MYL2, NAP1L1, NCF2, TRIM37, SLC16A4, SLC16A3, PDLIM1, B4GALT5, MT1B, NREP, ASIC3, S1PR2, MT1F, GPR37L1, MT1G, STK17A, AIMP1, NUMBL, MT1H, NOG, MT1M, MT1L, MT1X, SLC16A7, ARHGEF2, OSMR, COX1, EBAG9, MTNR1A, CCNB2, TUSC3, PDK4, NTT, SPOCK1, ST13, ST2, RBBP5, RBBP6, RBP1, SSRP1, ITPRID2, SREBF2, SRI, SRD5A1, SRC, SPI1, RNASE3, SP3, REN, DPF2, SOX5, REV3L, SOX1, SOS1, RGS3, SOD2, RGS4, RMRP, ST14, STAR, KDM5A, STAT2, VPS72, RAB2A, RAB3A, RAB3B, RAB6A, TBX1, RAC2, TAP1, TAL1, TACR1, RAC3, RAD51B, MOK, RAD52, VAMP7, RANGAP1, SULT1A1, RAP1B, STK4, STIM1, RAP2B, PLAAT4, RASA1, SNRNP70, RNF5, TFEB, TRA2B, SORT1, ST8SIA1, S100A11, SIAH1, SHOX2, S100A13, SAA4, SHBG, SH3GL3, TSPAN31, SGK1, SRSF3, ABCE1, SRSF1, SFRP4, SFRP2, SCN8A, MAP2K4, SEL1L, SDHD, SDHC, SCNN1D, CCL18, CX3CL1, RYR3, SIX3, SKI, RYK, SMPD1, RORA, RORB, SMARCB1, RPA3, SMARCA2, RPL11, RPL34, SLIT1, RPS6, SLC18A1, RPS6KA1, SLC9A5, RPS6KA3, RPS6KB1, RPS15, RRM1, SLC2A5, SLC2A3, RRM2, SLC1A3, SLC1A2, SLAMF1, PRDX2, TEAD1, PTPRJ, VCAM1, VTN, VSNL1, VRK1, VIP, PLP1, PLTP, PMP22, PMS1, PNLIP, VDAC2, VCL, VASP, TERF1, UTRN, POLB, USF1, UQCRC2, POMC, PON1, UGP2, POR, UCHL1, SUMO1, POU3F3, PLEK, WEE1, PLD2, WNT2, NELFE, PF4, PFN1, DAP3, DNALI1, PRDM2, ZYX, ZNF217, RNF112, ABCB4, ZNF143, PHB, PHEX, PIK3C2B, PKD1, PKP2, PLA2G5, PLAT, WRN, WNT2B, WNT11, PLCL1, PLCG1, UBE2I, U2AF1, TXNRD1, MAP2K2, PRL, TNFAIP2, PROP1, TMSB4X, TM7SF2, TSPAN8, LGMN, PRSS8, TKT, NKX2-1, TIMP3, KLK6, PSD, PSMB8, PSMD10, PTCH1, PTH, PTGS1, TFF3, PTPN9, PTPRA, PTPRC, PTPRF, MAP2K3, TP53BP1, MED1, TPD52, TNFSF4, PTPA, TTR, TTK, PPP5C, TSC2, PREP, TRPC5, SRGN, PRKACG, PRKCD, PRKCE, TRAF3, TRAF2, TRAF1, HSP90B1, NR2C2, CRISP2, PRKG2, MAPK7, TPM1, TPI1, TPD52L2, ARHGEF11, TRIM14, CIITA, UBE2S, CPS1-IT1, HIPK2, HOXA7, MRPL42, LAMTOR2, TRIB2, HOXA10, POLM, SGSM3, HOXA11, POLL, EIF3K, ZBTB32, BHLHE22, HOXA13, HOXB1, GLS2, HOXB7, INTU, HOXB9, EIF2AK1, HOXC4, HOXC8, LAT, HOXA5, LINC00339, NXT1, SAP30BP, MBL3P, HNRNPA1, HNRNPC, NOX4, HNRNPF, STOML2, EHD3, HNRNPK, ERVW-1, BICRA, HNRNPU, A1CF, RMC1, HOOK2, HOXA3, TRA2A, MYLPF, REPIN1, CARD10, TMOD4, UHRF1, HOXA4, BRD7, NOX1, MLH3, IL1RN, CLEC5A, QPCT, RASGRP3, POTEH, HTR1E, HTR2C, RAB38, HTR5A, HTR6, HYAL1, ID1, DAPK2, AMACR, HBP1, PATZ1, WBP2, PSD4, ID4, ZNF281, KCTD2, DAAM2, TNFRSF13B, IGFBP4, TRAM1, IGSF1, BAMBI, PRDX5, BRMS1, PRKD2, RANBP6, SNORD47, CKAP2, HOXD4, HOXD10, FBXO8, HPR, HRC, SERBP1, PRPF31, HRG, PRMT1, DNM3, CNTNAP2, KANK2, RWDD3, SYF2, CLIC4, ZDHHC5, HTR1A, LETMD1, MPC2, RPL36, PCA3, HNF4A, TRAT1, SAMD9, PINX1, SDHAF2, CMTM6, FOCAD, MKS1, ELOVL2, CASZ1, BCOR, EPS8L1, PGPEP1, ANKRD49, DYM, STMN3, ARHGAP35, TRIM44, IL17RD, GRM8, CXCL1, DDIT4, PDIA3, RIN2, TREM2, NANS, DCUN1D1, MCUB, PID1, GPX4, EPN3, GLUL, ASIC4, SAGE1, GNRHR, GPC1, HES6, GPD1, LGR4, STYK1, LAPTM4B, GPD2, GPI, CCR10, IMP3, STEAP3, APPL2, GRK5, GRK6, HEATR1, PIWIL2, AGGF1, ANO1, TMEM45A, GSTM2, GUCY1A1, XCL1, PHF21A, TLR7, GOLM1, NT5C3A, HLA-F, NUSAP1, CPA4, HERC5, PLEKHO1, HLA-G, HMGB2, HMGCR, IRAK4, GOLGA7, RMDN1, SH3GLB1, ADIPOR1, GAL, HMGA1, PLEKHA8P1, UBXN1, FIS1, TMED5, FOXA2, SLC22A17, TAOK3, TPCN1, HLA-DQA1, SHC3, IL17D, GALNT7, HDAC2, CMPK1, HEXA, RAB23, HEXB, TPPP3, GINS2, STYXL1, RASD1, PPIL1, SF3B6, KLF13, IL23A, HIVEP2, SIRT7, ISYNA1, POLK, HLA-DMA, CRLF3, ANGPT4, SLC44A1, NOMO1, MGAT5, C1D, SEMA4B, STK25, VAT1, HOXB13, SLC30A9, MERTK, LSS, MAD2L2, GPNMB, HAX1, LUM, IFI30, SMAD6, RBM14, LYN, LYZ, TACSTD2, CPQ, PIAS3, MAD2L1, SMAD1, TUBB3, IRF9, KLF2, LOXL2, LMO2, LLGL1, RNASEH2A, LAMC1, CELF2, CELF1, LBP, LCK, IGF2BP2, LDLR, LEP, NPRL2, RAD51AP1, LEPR, TXNIP, LIG1, PDLIM5, LIM2, SMC2, CCT4, MRPL28, SLC34A2, SLC35A1, SPTLC1, HTATIP2, LIMS1, HMG20B, CCNO, ZFPM2, RAB8A, ABCC5, SAE1, MCM7, CHAF1A, ME1, MEF2C, ZBTB33, MEFV, MAP3K1, HNRNPDL, TNFSF15, USP15, DLEU1, WDR1, P2RY14, MRC2, MEOX2, UBAP2L, SNAP91, TOX4, TLK1, SEC24D, MELTF, MGAT1, MCM6, DNM1L, MCM3, PPIF, APC2, CDK2AP2, ABCC4, MAG, SPRY1, TRIB1, MAGEA2, MAGEA6, MAOA, TNK2, WASF2, ATP6AP2, MAP1B, CEBPZ, MAS1, MBD1, BCAP31, OPTN, MBL2, ARL4A, MBP, MCAM, RAD50, EBP, LAMB2, CCT8, ITGB5, ATF6, CD93, ITGA4, ITGAX, FNDC3A, CILK1, CPEB3, PHLDA1, COPG1, ITGB4, OIP5, TUSC2, USP39, PDAP1, ACOT7, VSIG4, ITGB6, ITGB8, TREX1, TP53TG1, ITIH4, ITK, PTENP1, ITPKA, RAB18, ITGA2B, ELL2, RAB21, IL5, COTL1, IL6ST, CXCR2, NEDD4L, ICOSLG, PHLPP1, ARC, PLCB1, JMJD6, ACSBG1, FOXK2, LARP4B, ILF2, ING2, TOGARAM1, IQSEC2, KIF1B, ZNF423, INS, PDXDC1, MYT1L, IRF1, JAK1, JARID2, JUN, KCNQ1OT1, STIP1, KCNMB1, KHK, BRD8, MALT1, RAB10, KIF5B, PGRMC1, KLK2, KLC1, KPNB1, KPNA2, KRT1, LAMA4, TRAF3IP2, GIPC1, CHL1, LAMA5, PLK4, TCFL5, NFAT5, CERS1, LAMB1, CKAP4, COPS5, FSTL1, METAP2, SOX21, CD82, HHLA2, PTPRT, RPP14, ADAMTS5, ADAMTS8, ESM1, TRIOBP, TPPP, KCNA3, RAPGEF4, WWP2, WWP1, TENT4A, KCNA10, DSTN, KCNB1, KCNH1, KIF2C, SLC27A2, KCNK1, SLC38A3, SEMA7A
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Cystic Lesions Of The Pancreas
Wikipedia
PMID 20601810 . v t e Digestive system neoplasia GI tract Upper Esophagus Squamous cell carcinoma Adenocarcinoma Stomach Gastric carcinoma Signet ring cell carcinoma Gastric lymphoma MALT lymphoma Linitis plastica Lower Small intestine Duodenal cancer Adenocarcinoma Appendix Carcinoid Pseudomyxoma peritonei Colon/rectum Colorectal polyp : adenoma , hyperplastic , juvenile , sessile serrated adenoma , traditional serrated adenoma , Peutz–Jeghers Cronkhite–Canada Polyposis syndromes: Juvenile MUTYH-associated Familial adenomatous / Gardner's Polymerase proofreading-associated Serrated polyposis Neoplasm: Adenocarcinoma Familial adenomatous polyposis Hereditary nonpolyposis colorectal cancer Anus Squamous cell carcinoma Upper and/or lower Gastrointestinal stromal tumor Krukenberg tumor (metastatic) Accessory Liver malignant : Hepatocellular carcinoma Fibrolamellar Hepatoblastoma benign : Hepatocellular adenoma Cavernous hemangioma hyperplasia : Focal nodular hyperplasia Nodular regenerative hyperplasia Biliary tract bile duct : Cholangiocarcinoma Klatskin tumor gallbladder : Gallbladder cancer Pancreas exocrine pancreas : Adenocarcinoma Pancreatic ductal carcinoma cystic neoplasms : Serous microcystic adenoma Intraductal papillary mucinous neoplasm Mucinous cystic neoplasm Solid pseudopapillary neoplasm Pancreatoblastoma Peritoneum Primary peritoneal carcinoma Peritoneal mesothelioma Desmoplastic small round cell tumor
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Otitis
Wikipedia
External links [ edit ] Classification D ICD - 9-CM : 380.10 MeSH : D010031 External resources MedlinePlus : 001336 v t e Diseases of the outer and middle ear Outer ear Otitis externa Otomycosis Middle ear and mastoid Otitis media Mastoiditis Bezold's abscess Gradenigo's syndrome Tympanosclerosis Cholesteatoma Perforated eardrum Symptoms Ear pain Hearing loss Tests Otoscope pneumatic tympanometry v t e Inflammation Symptoms Flushing (Rubor) Fever (Calor) Swelling (Tumor) Pain (Dolor) Malaise Mechanism Acute Plasma-derived mediators Bradykinin complement C3 C5a MAC coagulation Factor XII Plasmin Thrombin Cell-derived mediators preformed: Lysosome granules biogenic amines Histamine Serotonin synthesized on demand: cytokines IFN-γ IL-8 TNF-α IL-1 eicosanoids Leukotriene B4 Prostaglandins Nitric oxide Kinins Chronic Macrophage Epithelioid cell Giant cell Granuloma Other Acute-phase reaction Vasodilation Increased vascular permeability Exudate Leukocyte extravasation Chemotaxis Tests Full blood count Leukocytosis C-reactive protein Erythrocyte sedimentation rate General Lymphadenopathy List of inflammed body part states This article about a disease of the ear and mastoid process is a stub .
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Combined Immunodeficiency Due To Crac Channel Dysfunction
Orphanet
Differential diagnosis Differential diagnoses include combined immunodeficiency (CID) due to ZAP70 deficiency, CID due to CD3gamma deficiency, immunodeficiency due to CD25 deficiency, hypohidrotic ectodermal dysplasia with immunodeficiency and anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema syndrome. Antenatal diagnosis Prenatal diagnosis can be performed where there is a family history and where the genetic mutation has been identified.
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Muscular Dystrophy, Scapulohumeral
Omim
There were no contractures or dysarthria, distinguishing this syndrome from autosomal dominant limb-girdle dystrophy (253600) which typically begins with symptoms in the lower extremities.DUX4, SMCHD1, FRG1, DUX4L1, LUM, ACAN, ELN, DCN, GSTT2, HSPA1B, HSPA4, CDKN1A, COL3A1, FAT1, LARGE1, FSHMD1A, FLNA, FRG2, DMD, SAT2, DUX4L2, LOC107987484, LOC107987485, LOC107987486, LOC107987487, SLC25A4, FXR1, PRPF6, PAX7, IL2, IFNG, DNMT3B, DUX4L9, SLC38A2, PDLIM3, CAPN3, CTCF, PITX1, EIF3K, SGSM3, DBET, SEA, BRD2, LMNA, SUMF2, RGCC, POLDIP2, ATRNL1, RNF19A, ESR2, PSD4, CD44, KLF15, DCTN3, CCL27, AHSA1, CXCL13, FST, G3BP1, CHAF1A, GRAP2, CDC27, LRP2BP, CNOT7, CAV2, ANXA13, ARNTL, ZASP, MIR1307, ATHS, C1QBP, MIR411, H4C15, MIR206, H4-16, SPECC1, RBFOX1, MBD3L1, ASRGL1, IL21, RTN4, PCBP4, ASH1L, PAG1, CNOT8, FBXW7, NAT10, ZFYVE9, H4C5, CDKN3, IL4, PMP22, PCNT, PAX3, MYH7, MYF5, CREBBP, ITGB6, IRF2, IRF1, IL10, IL6, HSPG2, CCNA1, CRK, CRYM, MAPK14, MSTN, FSHMD1B, EIF4E, EMD, FHL1, FGF2, FGF1, EP300, PPIA, MAPK1, OPN1LW, RTN1, H4C14, H4C13, EWSR1, H4C2, H4C8, H4C3, H4C11, H4C12, H4C6, H4C4, H4C1, H4C9, CHAF1B, FOSL1, ALPP, TP53, TIMP3, TACR2, SLPI, SKP1, ST3GAL4, SDC2, CCL20, AIMP2
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Tay-Sachs Disease
Orphanet
The second is that of juvenile spinal amyotrophy resembling Kugelberg-Welander's syndrome. Mental capacities and behaviour may or may not be affected.
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X-Linked Spondyloepiphyseal Dysplasia Tarda
Gene_reviews
COL2A1 COL9A1 COL9A2 COL9A3 COL11A1 COL11A2 Stickler syndrome AD AR 2 Connective tissue disorder; can incl high myopia, hearing loss (both conductive & sensorineural); midfacial underdevelopment & cleft palate (either alone or as part of Robin sequence); & mild SED &/or precocious arthritis. ... By definition, spine in MED is normal, although Schmorl bodies & irregular vertebral end plates may be observed. GALNS GLB1 Morquio syndrome (MPS IVA & MPS IVB) (See GLB1 Disorders.) ... Rare instances of autosomal recessive inheritance in SEDC have been reported (see Type II Collagen Disorders Overview). 2. Stickler syndrome caused by pathogenic variants in COL2A1 , COL11A1 , or COL11A2 is inherited in an autosomal dominant manner; Stickler syndrome caused by pathogenic variants in COL9A1 , COL9A2 , or COL9A3 is inherited in an autosomal recessive manner.
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Electroanalgesia
Wikipedia
Transcranial electrostimulation [ edit ] A theoretical explanation for the mechanism of pain reduction by transcranial electrostimulation, or TCES, suggests that the electrical stimulation activates the anti-nociceptive system in the brain, resulting in β-endorphin, serotonin and noradrenaline release. [3] TCES can be used on people with cervical pain, chronic lower back syndrome, or migraines. [3] It cannot be used on people with orthopedic or radiological potentially serious spinal conditions, hydrocephalus , epilepsy , glaucoma , malignant hypertension , pacemaker or other implanted electronic device; recent cerebral trauma , nervous system infection, skin lesions at sites of electrode placement; oncological disease; patients undergoing any other treatments for pain; any invasive therapy, e.g. surgery, within the last month. [3] The equipment used is Pulse Mazor Instruments' Pulsatilla 1000 , which consists of a headset with three electrodes , two that go behind the ears and one that goes on the forehead, that release set frequencies of electricity at set intervals. ... It is effective in treating refractory post-stroke pain, atypical face pain, anaesthesia dolorosa, and deafferentation and somatic pain such as in phantom limb or brachial plexus injury (Boccard et al. 2013). [5] Peripheral nerve stimulation [ edit ] The use of peripheral nerve stimulation, or PNS, for the relief of chronic pain states was first reported over 30 years ago. [6] Recent studies have demonstrated that electrical stimulation of nerves leads to inhibitory input to the pain pathways at the spinal cord level. [7] PNS is most effective in the treatment of neuropathic pain (e.g., posttraumatic neuropathy, diabetic neuropathy) when the nerve lesion is distal to the site of stimulation. [8] Percutaneous electrical nerve stimulation [ edit ] Percutaneous electrical nerve stimulation, or PENS, is used mainly in the treatment of intractable pain associated with chronic low back pain syndrome, cancer, and other disorders. [8] It is a technique involving insertion of an ultra-fine acupuncture needle which probes into the soft tissues or muscles to electrically stimulate nerve fibers in the sclerotomal , myotomal , or dermatomal distribution corresponding to the patient's pain symptoms. ... It has been used in the treatment of pain related to diabetic neuropathy , muscle sprains , temporomandibular joint disorders , type I complex regional pain syndrome as well as the healing of wounds such as diabetic ulcers . [14] [15] This electroanalgesic modality was originally recommended as an alternative to TENS for dental analgesia. ... Although ICT is used widely in the physiotherapy and rehabilitative medicine settings, there is a dearth of rigorously controlled studies to justify its effectiveness in the management of either acute or chronic pain syndromes. [8] Piezo-electric current therapy [ edit ] Piezo-electric current therapy, or PECT, is an analgesic technique based on the principle that mechanical deformation of a motorized piezoelectric ceramic rod produces a burst of 10 electrical pulses (five positive and five negative), each lasting 2–3 ms .
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Laryngotracheal Stenosis
Wikipedia
External links [ edit ] Classification D ICD - 10 : Q31.1 , Q32.1 , J38.6 , J39.8 , J95.5 ICD - 9-CM : 519.19 , 748.3 MeSH : D014135 v t e Diseases of the respiratory system Upper RT (including URTIs , common cold ) Head sinuses Sinusitis nose Rhinitis Vasomotor rhinitis Atrophic rhinitis Hay fever Nasal polyp Rhinorrhea nasal septum Nasal septum deviation Nasal septum perforation Nasal septal hematoma tonsil Tonsillitis Adenoid hypertrophy Peritonsillar abscess Neck pharynx Pharyngitis Strep throat Laryngopharyngeal reflux (LPR) Retropharyngeal abscess larynx Croup Laryngomalacia Laryngeal cyst Laryngitis Laryngopharyngeal reflux (LPR) Laryngospasm vocal cords Laryngopharyngeal reflux (LPR) Vocal fold nodule Vocal fold paresis Vocal cord dysfunction epiglottis Epiglottitis trachea Tracheitis Laryngotracheal stenosis Lower RT / lung disease (including LRTIs ) Bronchial / obstructive acute Acute bronchitis chronic COPD Chronic bronchitis Acute exacerbation of COPD ) Asthma ( Status asthmaticus Aspirin-induced Exercise-induced Bronchiectasis Cystic fibrosis unspecified Bronchitis Bronchiolitis Bronchiolitis obliterans Diffuse panbronchiolitis Interstitial / restrictive ( fibrosis ) External agents/ occupational lung disease Pneumoconiosis Aluminosis Asbestosis Baritosis Bauxite fibrosis Berylliosis Caplan's syndrome Chalicosis Coalworker's pneumoconiosis Siderosis Silicosis Talcosis Byssinosis Hypersensitivity pneumonitis Bagassosis Bird fancier's lung Farmer's lung Lycoperdonosis Other ARDS Combined pulmonary fibrosis and emphysema Pulmonary edema Löffler's syndrome / Eosinophilic pneumonia Respiratory hypersensitivity Allergic bronchopulmonary aspergillosis Hamman-Rich syndrome Idiopathic pulmonary fibrosis Sarcoidosis Vaping-associated pulmonary injury Obstructive / Restrictive Pneumonia / pneumonitis By pathogen Viral Bacterial Pneumococcal Klebsiella Atypical bacterial Mycoplasma Legionnaires' disease Chlamydiae Fungal Pneumocystis Parasitic noninfectious Chemical / Mendelson's syndrome Aspiration / Lipid By vector/route Community-acquired Healthcare-associated Hospital-acquired By distribution Broncho- Lobar IIP UIP DIP BOOP-COP NSIP RB Other Atelectasis circulatory Pulmonary hypertension Pulmonary embolism Lung abscess Pleural cavity / mediastinum Pleural disease Pleuritis/pleurisy Pneumothorax / Hemopneumothorax Pleural effusion Hemothorax Hydrothorax Chylothorax Empyema/pyothorax Malignant Fibrothorax Mediastinal disease Mediastinitis Mediastinal emphysema Other/general Respiratory failure Influenza Common cold SARS Coronavirus disease 2019 Idiopathic pulmonary haemosiderosis Pulmonary alveolar proteinosis v t e Congenital malformations and deformations of respiratory system Upper RT Nose Choanal atresia Arrhinia Larynx Laryngeal cyst Laryngocele Laryngomalacia Lower RT Trachea and bronchus Tracheomalacia Tracheal stenosis Bronchomalacia Tracheobronchomegaly Lung Bronchiectasis Pulmonary hypoplasia Pulmonary sequestration Congenital cystic adenomatoid malformation
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Coronary Artery Anomaly
Wikipedia
External links [ edit ] Classification D ICD - 10 : Q24.5 ICD - 9-CM : 746.85 MeSH : D003330 DiseasesDB : 34206 External resources eMedicine : med/445 ped/2506 v t e Congenital heart defects Heart septal defect Aortopulmonary septal defect Double outlet right ventricle Taussig–Bing syndrome Transposition of the great vessels dextro levo Persistent truncus arteriosus Aortopulmonary window Atrial septal defect Sinus venosus atrial septal defect Lutembacher's syndrome Ventricular septal defect Tetralogy of Fallot Atrioventricular septal defect Ostium primum Consequences Cardiac shunt Cyanotic heart disease Eisenmenger syndrome Valvular heart disease Right pulmonary valves stenosis insufficiency absence tricuspid valves stenosis atresia Ebstein's anomaly Left aortic valves stenosis insufficiency bicuspid mitral valves stenosis regurgitation Other Underdeveloped heart chambers right left Uhl anomaly Dextrocardia Levocardia Cor triatriatum Crisscross heart Brugada syndrome Coronary artery anomaly Anomalous aortic origin of a coronary artery Ventricular inversion
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Acute Bronchitis
Wikipedia
National Library of Medicine. v t e Diseases of the respiratory system Upper RT (including URTIs , common cold ) Head sinuses Sinusitis nose Rhinitis Vasomotor rhinitis Atrophic rhinitis Hay fever Nasal polyp Rhinorrhea nasal septum Nasal septum deviation Nasal septum perforation Nasal septal hematoma tonsil Tonsillitis Adenoid hypertrophy Peritonsillar abscess Neck pharynx Pharyngitis Strep throat Laryngopharyngeal reflux (LPR) Retropharyngeal abscess larynx Croup Laryngomalacia Laryngeal cyst Laryngitis Laryngopharyngeal reflux (LPR) Laryngospasm vocal cords Laryngopharyngeal reflux (LPR) Vocal fold nodule Vocal fold paresis Vocal cord dysfunction epiglottis Epiglottitis trachea Tracheitis Laryngotracheal stenosis Lower RT / lung disease (including LRTIs ) Bronchial / obstructive acute Acute bronchitis chronic COPD Chronic bronchitis Acute exacerbation of COPD ) Asthma ( Status asthmaticus Aspirin-induced Exercise-induced Bronchiectasis Cystic fibrosis unspecified Bronchitis Bronchiolitis Bronchiolitis obliterans Diffuse panbronchiolitis Interstitial / restrictive ( fibrosis ) External agents/ occupational lung disease Pneumoconiosis Aluminosis Asbestosis Baritosis Bauxite fibrosis Berylliosis Caplan's syndrome Chalicosis Coalworker's pneumoconiosis Siderosis Silicosis Talcosis Byssinosis Hypersensitivity pneumonitis Bagassosis Bird fancier's lung Farmer's lung Lycoperdonosis Other ARDS Combined pulmonary fibrosis and emphysema Pulmonary edema Löffler's syndrome / Eosinophilic pneumonia Respiratory hypersensitivity Allergic bronchopulmonary aspergillosis Hamman-Rich syndrome Idiopathic pulmonary fibrosis Sarcoidosis Vaping-associated pulmonary injury Obstructive / Restrictive Pneumonia / pneumonitis By pathogen Viral Bacterial Pneumococcal Klebsiella Atypical bacterial Mycoplasma Legionnaires' disease Chlamydiae Fungal Pneumocystis Parasitic noninfectious Chemical / Mendelson's syndrome Aspiration / Lipid By vector/route Community-acquired Healthcare-associated Hospital-acquired By distribution Broncho- Lobar IIP UIP DIP BOOP-COP NSIP RB Other Atelectasis circulatory Pulmonary hypertension Pulmonary embolism Lung abscess Pleural cavity / mediastinum Pleural disease Pleuritis/pleurisy Pneumothorax / Hemopneumothorax Pleural effusion Hemothorax Hydrothorax Chylothorax Empyema/pyothorax Malignant Fibrothorax Mediastinal disease Mediastinitis Mediastinal emphysema Other/general Respiratory failure Influenza Common cold SARS Coronavirus disease 2019 Idiopathic pulmonary haemosiderosis Pulmonary alveolar proteinosis v t e Common cold Viruses Adenovirus Coronavirus Enterovirus Rhinovirus Symptoms Cough Fatigue Fever Headache Loss of appetite Malaise Muscle aches Nasal congestion Rhinorrhea Sneezing Sore throat Weakness Complications Acute bronchitis Bronchiolitis Croup Otitis media Pharyngitis Pneumonia Sinusitis Strep throat Drugs Antiviral drugs Pleconaril (experimental)
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Reflex Seizure
Wikipedia
Reflex seizure Specialty Neurology Symptoms Seizures due to a specific trigger [1] Treatment Decreasing exposure to triggers, anti-epileptic medications [2] [3] Frequency Relatively rare [3] Reflex seizures are epileptic seizures that are consistently induced by a specific stimulus or trigger making them distinct from other epileptic seizures, which are usually unprovoked. [4] [3] Reflex seizures are otherwise similar to unprovoked seizures and may be focal (simple or complex), generalized , myoclonic , or absence seizures. [1] Epilepsy syndromes characterized by repeated reflex seizures are known as reflex epilepsies . [3] [4] Photosensitive seizures are often myoclonic, absence, or focal seizures in the occipital lobe , while musicogenic seizures are associated with focal seizures in the temporal lobe . [3] Triggers may include various stimuli with the most common (75 to 80%) being flickering lights resulting in photosensitive seizures . [3] Reflex epilepsies are generally thought to be genetic in origin. [3] The inheritance pattern is dependent on the type of reflex epilepsy with some types lacking a specific genetic inheritance patterns. [3] For example, photogenic epilepsy is thought to follow an autosomal dominant pattern with incomplete penetrance , while seizures triggered by proprioceptive stimuli do not follow an observable inheritance pattern. [3] The underlying mechanism involves the stimulation of existing network of neurons by the specific trigger. [3] The treatment of reflex epilepsy generally involves decreasing exposure to a person's triggers as well as anti-epileptic medications . [2] [3] Reflex epilepsy is relatively rare, making up approximately 5% of epilepsy syndromes. [3] Contents 1 Signs and symptoms 1.1 Generalized seizures 1.2 Focal seizures 1.3 Triggers 1.3.1 Extrinsic stimuli 1.3.2 Intrinsic stimuli 2 Cause 3 Pathophysiology 4 Diagnosis 5 Treatment 5.1 Photosensitive epilepsy 6 Epidemiology 7 History 8 References 9 External links Signs and symptoms [ edit ] Reflex seizures can be either generalized or focal seizures or both. [2] However, for any given stimulus there may be a large variation in the kind of elicited seizure. ... Determining if this seizure or seizures are a part of a specific epilepsy syndrome or disease. Treatment [ edit ] The treatment of reflex epilepsy generally involves decreasing exposure to a person's triggers as well as anti-epileptic medications . [2] [3] Specific treatment depends both on the person as well on the kind of reflex triggers. [2] For example, in photosensitive epilepsy, some people may rely only on managing exposure to their triggers, while others, may benefit greatly from anti-epileptic drugs. [2] In addition, different anti-epileptic medications may be used in order to treat a given person's reflex epilepsy depending on the kind of seizures that they experience. [2] Photosensitive epilepsy [ edit ] Photosensitive reflex epilepsy is usually treated with both lifestyle changes and anti-epileptic medications. ... S2CID 21228396 . ^ a b c Panayiotopoulos, CP (2010). A Clinical Guide to Epileptic Syndromes and their Treatment . Springer.
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Biphenotypic Acute Leukaemia
Wikipedia
External links [ edit ] Classification D ICD-O : 9805/3 MeSH : D015456 v t e Leukaemias , lymphomas and related disease B cell ( lymphoma , leukemia ) (most CD19 CD20 ) By development/ marker TdT+ ALL ( Precursor B acute lymphoblastic leukemia/lymphoma ) CD5 + naive B cell ( CLL/SLL ) mantle zone ( Mantle cell ) CD22 + Prolymphocytic CD11c+ ( Hairy cell leukemia ) CD79a + germinal center / follicular B cell ( Follicular Burkitt's GCB DLBCL Primary cutaneous follicle center lymphoma ) marginal zone / marginal zone B-cell ( Splenic marginal zone MALT Nodal marginal zone Primary cutaneous marginal zone lymphoma ) RS ( CD15 +, CD30 +) Classic Hodgkin lymphoma ( Nodular sclerosis ) CD20+ ( Nodular lymphocyte predominant Hodgkin lymphoma ) PCDs / PP ( CD38 +/ CD138 +) see immunoproliferative immunoglobulin disorders By infection KSHV ( Primary effusion ) EBV Lymphomatoid granulomatosis Post-transplant lymphoproliferative disorder Classic Hodgkin lymphoma Burkitt's lymphoma HCV Splenic marginal zone lymphoma HIV ( AIDS-related lymphoma ) Helicobacter pylori ( MALT lymphoma ) Cutaneous Diffuse large B-cell lymphoma Intravascular large B-cell lymphoma Primary cutaneous marginal zone lymphoma Primary cutaneous immunocytoma Plasmacytoma Plasmacytosis Primary cutaneous follicle center lymphoma T/NK T cell ( lymphoma , leukemia ) (most CD3 CD4 CD8 ) By development/ marker TdT+ : ALL ( Precursor T acute lymphoblastic leukemia/lymphoma ) prolymphocyte ( Prolymphocytic ) CD30+ ( Anaplastic large-cell lymphoma Lymphomatoid papulosis type A ) Cutaneous MF+variants indolent: Mycosis fungoides Pagetoid reticulosis Granulomatous slack skin aggressive: Sézary disease Adult T-cell leukemia/lymphoma Non-MF CD30 -: Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma Pleomorphic T-cell lymphoma Lymphomatoid papulosis type B CD30 +: CD30+ cutaneous T-cell lymphoma Secondary cutaneous CD30+ large-cell lymphoma Lymphomatoid papulosis type A Other peripheral Hepatosplenic Angioimmunoblastic Enteropathy-associated T-cell lymphoma Peripheral T-cell lymphoma not otherwise specified ( Lennert lymphoma ) Subcutaneous T-cell lymphoma By infection HTLV-1 ( Adult T-cell leukemia/lymphoma ) NK cell / (most CD56 ) Aggressive NK-cell leukemia Blastic NK cell lymphoma T or NK EBV ( Extranodal NK-T-cell lymphoma / Angiocentric lymphoma ) Large granular lymphocytic leukemia Lymphoid+ myeloid Acute biphenotypic leukaemia Lymphocytosis Lymphoproliferative disorders ( X-linked lymphoproliferative disease Autoimmune lymphoproliferative syndrome ) Leukemoid reaction Diffuse infiltrative lymphocytosis syndrome Cutaneous lymphoid hyperplasia Cutaneous lymphoid hyperplasia with bandlike and perivascular patterns with nodular pattern Jessner lymphocytic infiltrate of the skin General Hematological malignancy leukemia Lymphoproliferative disorders Lymphoid leukemias v t e Myeloid -related hematological malignancy CFU-GM / and other granulocytes CFU-GM Myelocyte AML : Acute myeloblastic leukemia M0 M1 M2 APL/M3 MP Chronic neutrophilic leukemia Monocyte AML AMoL/M5 Myeloid dendritic cell leukemia CML Philadelphia chromosome Accelerated phase chronic myelogenous leukemia Myelomonocyte AML M4 MD-MP Juvenile myelomonocytic leukemia Chronic myelomonocytic leukemia Other Histiocytosis CFU-Baso AML Acute basophilic CFU-Eos AML Acute eosinophilic MP Chronic eosinophilic leukemia / Hypereosinophilic syndrome MEP CFU-Meg MP Essential thrombocytosis Acute megakaryoblastic leukemia CFU-E AML Erythroleukemia/M6 MP Polycythemia vera MD Refractory anemia Refractory anemia with excess of blasts Chromosome 5q deletion syndrome Sideroblastic anemia Paroxysmal nocturnal hemoglobinuria Refractory cytopenia with multilineage dysplasia CFU-Mast Mastocytoma Mast cell leukemia Mast cell sarcoma Systemic mastocytosis Mastocytosis : Diffuse cutaneous mastocytosis Erythrodermic mastocytosis Adult type of generalized eruption of cutaneous mastocytosis Urticaria pigmentosa Mast cell sarcoma Solitary mastocytoma Systemic mastocytosis Xanthelasmoidal mastocytosis Multiple/unknown AML Acute panmyelosis with myelofibrosis Myeloid sarcoma MP Myelofibrosis Acute biphenotypic leukaemia
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Tinea Capitis
Wikipedia
External links [ edit ] Classification D ICD - 10 : B35.0 ( ILDS B35.006) ICD - 9-CM : 110.0 MeSH : D014006 DiseasesDB : 13117 External resources MedlinePlus : 000878 eMedicine : derm/420 v t e Diseases of the skin and appendages by morphology Growths Epidermal Wart Callus Seborrheic keratosis Acrochordon Molluscum contagiosum Actinic keratosis Squamous-cell carcinoma Basal-cell carcinoma Merkel-cell carcinoma Nevus sebaceous Trichoepithelioma Pigmented Freckles Lentigo Melasma Nevus Melanoma Dermal and subcutaneous Epidermal inclusion cyst Hemangioma Dermatofibroma (benign fibrous histiocytoma) Keloid Lipoma Neurofibroma Xanthoma Kaposi's sarcoma Infantile digital fibromatosis Granular cell tumor Leiomyoma Lymphangioma circumscriptum Myxoid cyst Rashes With epidermal involvement Eczematous Contact dermatitis Atopic dermatitis Seborrheic dermatitis Stasis dermatitis Lichen simplex chronicus Darier's disease Glucagonoma syndrome Langerhans cell histiocytosis Lichen sclerosus Pemphigus foliaceus Wiskott–Aldrich syndrome Zinc deficiency Scaling Psoriasis Tinea ( Corporis Cruris Pedis Manuum Faciei ) Pityriasis rosea Secondary syphilis Mycosis fungoides Systemic lupus erythematosus Pityriasis rubra pilaris Parapsoriasis Ichthyosis Blistering Herpes simplex Herpes zoster Varicella Bullous impetigo Acute contact dermatitis Pemphigus vulgaris Bullous pemphigoid Dermatitis herpetiformis Porphyria cutanea tarda Epidermolysis bullosa simplex Papular Scabies Insect bite reactions Lichen planus Miliaria Keratosis pilaris Lichen spinulosus Transient acantholytic dermatosis Lichen nitidus Pityriasis lichenoides et varioliformis acuta Pustular Acne vulgaris Acne rosacea Folliculitis Impetigo Candidiasis Gonococcemia Dermatophyte Coccidioidomycosis Subcorneal pustular dermatosis Hypopigmented Tinea versicolor Vitiligo Pityriasis alba Postinflammatory hyperpigmentation Tuberous sclerosis Idiopathic guttate hypomelanosis Leprosy Hypopigmented mycosis fungoides Without epidermal involvement Red Blanchable Erythema Generalized Drug eruptions Viral exanthems Toxic erythema Systemic lupus erythematosus Localized Cellulitis Abscess Boil Erythema nodosum Carcinoid syndrome Fixed drug eruption Specialized Urticaria Erythema ( Multiforme Migrans Gyratum repens Annulare centrifugum Ab igne ) Nonblanchable Purpura Macular Thrombocytopenic purpura Actinic/solar purpura Papular Disseminated intravascular coagulation Vasculitis Indurated Scleroderma / morphea Granuloma annulare Lichen sclerosis et atrophicus Necrobiosis lipoidica Miscellaneous disorders Ulcers Hair Telogen effluvium Androgenic alopecia Alopecia areata Systemic lupus erythematosus Tinea capitis Loose anagen syndrome Lichen planopilaris Folliculitis decalvans Acne keloidalis nuchae Nail Onychomycosis Psoriasis Paronychia Ingrown nail Mucous membrane Aphthous stomatitis Oral candidiasis Lichen planus Leukoplakia Pemphigus vulgaris Mucous membrane pemphigoid Cicatricial pemphigoid Herpesvirus Coxsackievirus Syphilis Systemic histoplasmosis Squamous-cell carcinoma v t e Fungal infection and mesomycetozoea Superficial and cutaneous ( dermatomycosis ): Tinea = skin ; Piedra ( exothrix / endothrix ) = hair Ascomycota Dermatophyte ( Dermatophytosis ) By location Tinea barbae / tinea capitis Kerion Tinea corporis Ringworm Dermatophytids Tinea cruris Tinea manuum Tinea pedis (athlete's foot) Tinea unguium/onychomycosis White superficial onychomycosis Distal subungual onychomycosis Proximal subungual onychomycosis Tinea corporis gladiatorum Tinea faciei Tinea imbricata Tinea incognito Favus By organism Epidermophyton floccosum Microsporum canis Microsporum audouinii Trichophyton interdigitale/mentagrophytes Trichophyton tonsurans Trichophyton schoenleini Trichophyton rubrum Trichophyton verrucosum Other Hortaea werneckii Tinea nigra Piedraia hortae Black piedra Basidiomycota Malassezia furfur Tinea versicolor Pityrosporum folliculitis Trichosporon White piedra Subcutaneous , systemic , and opportunistic Ascomycota Dimorphic (yeast+mold) Onygenales Coccidioides immitis / Coccidioides posadasii Coccidioidomycosis Disseminated coccidioidomycosis Primary cutaneous coccidioidomycosis .
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Primary Progressive Aphasia
Wikipedia
Specialty Neurology Primary progressive aphasia ( PPA ) is a type of neurological syndrome in which language capabilities slowly and progressively become impaired. ... It was first described as a distinct syndrome by M.‑Marsel Mesulam in 1982. [2] Primary progressive aphasias have a clinical and pathological overlap with the frontotemporal lobar degeneration (FTLD) spectrum of disorders and Alzheimer's disease . ... External links [ edit ] Classification D OMIM : 607485 MeSH : D018888 Topics related to Primary progressive aphasia v t e Diseases of the nervous system , primarily CNS Inflammation Brain Encephalitis Viral encephalitis Herpesviral encephalitis Limbic encephalitis Encephalitis lethargica Cavernous sinus thrombosis Brain abscess Amoebic Brain and spinal cord Encephalomyelitis Acute disseminated Meningitis Meningoencephalitis Brain / encephalopathy Degenerative Extrapyramidal and movement disorders Basal ganglia disease Parkinsonism PD Postencephalitic NMS PKAN Tauopathy PSP Striatonigral degeneration Hemiballismus HD OA Dyskinesia Dystonia Status dystonicus Spasmodic torticollis Meige's Blepharospasm Athetosis Chorea Choreoathetosis Myoclonus Myoclonic epilepsy Akathisia Tremor Essential tremor Intention tremor Restless legs Stiff-person Dementia Tauopathy Alzheimer's Early-onset Primary progressive aphasia Frontotemporal dementia / Frontotemporal lobar degeneration Pick's Dementia with Lewy bodies Posterior cortical atrophy Vascular dementia Mitochondrial disease Leigh syndrome Demyelinating Autoimmune Inflammatory Multiple sclerosis For more detailed coverage, see Template:Demyelinating diseases of CNS Episodic/ paroxysmal Seizures and epilepsy Focal Generalised Status epilepticus For more detailed coverage, see Template:Epilepsy Headache Migraine Cluster Tension For more detailed coverage, see Template:Headache Cerebrovascular TIA Stroke For more detailed coverage, see Template:Cerebrovascular diseases Other Sleep disorders For more detailed coverage, see Template:Sleep CSF Intracranial hypertension Hydrocephalus Normal pressure hydrocephalus Choroid plexus papilloma Idiopathic intracranial hypertension Cerebral edema Intracranial hypotension Other Brain herniation Reye syndrome Hepatic encephalopathy Toxic encephalopathy Hashimoto's encephalopathy Both/either Degenerative SA Friedreich's ataxia Ataxia–telangiectasia MND UMN only: Primary lateral sclerosis Pseudobulbar palsy Hereditary spastic paraplegia LMN only: Distal hereditary motor neuronopathies Spinal muscular atrophies SMA SMAX1 SMAX2 DSMA1 Congenital DSMA Spinal muscular atrophy with lower extremity predominance (SMALED) SMALED1 SMALED2A SMALED2B SMA-PCH SMA-PME Progressive muscular atrophy Progressive bulbar palsy Fazio–Londe Infantile progressive bulbar palsy both: Amyotrophic lateral sclerosisGRN, TARDBP, C9orf72, APOE, LAMC2, MAPT, CSF2, NEFL, SMUG1, IGFALS, ECD, PRNP, ACHE, SOD1, TOMM40, TNFRSF10B, PSIP1, KHSRP, VCP, RIDA, ABAT, TNFRSF1B, SIGLEC7, BBC3, TREM2, IL33, FOXP2, LRRK2, BPIFA2, TP53, PTPN4, TCF3, TCF4, ALOX5, APOC1, BDNF, CAT, CHI3L1, CUX1, GBA, HCLS1, IL2RB, MSMB, PPA1, PSPN, PSEN1, PSPH, PTEN, REG1A, STXBP3, AOS
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Hand, Foot, And Mouth Disease
Wikipedia
"Hand, foot, and mouth disease: Identifying and managing an acute viral syndrome" . Cleve Clin J Med . 81 (9): 537–43. doi : 10.3949/ccjm.81a.13132 . ... External links [ edit ] Classification D ICD - 10 : B08.4 ICD - 9-CM : 074.3 MeSH : D006232 DiseasesDB : 5622 External resources MedlinePlus : 000965 eMedicine : derm/175 Patient UK : Hand, foot, and mouth disease Media related to Hand, foot and mouth disease at Wikimedia Commons Highly contagious Hand, foot and mouth disease killing China's children at Wikinews v t e Skin infections , symptoms and signs related to viruses DNA virus Herpesviridae Alpha HSV Herpes simplex Herpetic whitlow Herpes gladiatorum Herpes simplex keratitis Herpetic sycosis Neonatal herpes simplex Herpes genitalis Herpes labialis Eczema herpeticum Herpetiform esophagitis Herpes B virus B virus infection VZV Chickenpox Herpes zoster Herpes zoster oticus Ophthalmic zoster Disseminated herpes zoster Zoster-associated pain Modified varicella-like syndrome Beta Human herpesvirus 6 / Roseolovirus Exanthema subitum Roseola vaccinia Cytomegalic inclusion disease Gamma KSHV Kaposi's sarcoma Poxviridae Ortho Variola Smallpox Alastrim MoxV Monkeypox CPXV Cowpox VV Vaccinia Generalized vaccinia Eczema vaccinatum Progressive vaccinia Buffalopox Para Farmyard pox : Milker's nodule Bovine papular stomatitis Pseudocowpox Orf Sealpox Other Yatapoxvirus : Tanapox Yaba monkey tumor virus MCV Molluscum contagiosum Papillomaviridae HPV Wart / plantar wart Heck's disease Genital wart giant Laryngeal papillomatosis Butcher's wart Bowenoid papulosis Epidermodysplasia verruciformis Verruca plana Pigmented wart Verrucae palmares et plantares BPV Equine sarcoid Parvoviridae Parvovirus B19 Erythema infectiosum Reticulocytopenia Papular purpuric gloves and socks syndrome Polyomaviridae Merkel cell polyomavirus Merkel cell carcinoma RNA virus Paramyxoviridae MeV Measles Togaviridae Rubella virus Rubella Congenital rubella syndrome ("German measles" ) Alphavirus infection Chikungunya fever Picornaviridae CAV Hand, foot, and mouth disease Herpangina FMDV Foot-and-mouth disease Boston exanthem disease Ungrouped Asymmetric periflexural exanthem of childhood Post-vaccination follicular eruption Lipschütz ulcer Eruptive pseudoangiomatosis Viral-associated trichodysplasia Gianotti–Crosti syndrome v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth Pulp calcification Pulp stone Pulp canal obliteration Pulp necrosis Pulp polyp Pulpitis Regional odontodysplasia Resorption Shovel-shaped incisors Supernumerary root Taurodontism Trauma Avulsion Cracked tooth syndrome Vertical root fracture Occlusal Tooth loss Edentulism Tooth wear Abrasion Abfraction Acid erosion Attrition Periodontium ( gingiva , periodontal ligament , cementum , alveolus ) – Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival erythema Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething Periapical, mandibular and maxillary hard tissues – Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Micrognathia Intraosseous cysts Odontogenic : periapical Dentigerous Buccal bifurcation Lateral periodontal Globulomaxillary Calcifying odontogenic Glandular odontogenic Non-odontogenic: Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget's disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis Temporomandibular joints , muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Acinic cell carcinoma Adenocarcinoma Adenoid cystic carcinoma Carcinoma ex pleomorphic adenoma Lymphoma Mucoepidermoid carcinoma Sclerosing polycystic adenosis Sialadenitis Parotitis Chronic sclerosing sialadenitis Sialectasis Sialocele Sialodochitis Sialosis Sialolithiasis Sjögren's syndrome Orofacial soft tissues – Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease Authority control NDL : 00804612CA10, CXCL8, IL10, IL6, TNF, VDR, AQP4, IL18, IFNG, TLR3, OAS1, SCARB2, CCL2, IL22, VIP, CCL4L2, CERS1, ATG4B, TLR4, DDX58, IL37, ACTB, DLL1, SLC6A1, TLR7, TLR8, SCARA3, GDE1, DLL4, ROBO3, IL17F, MIR155HG, CCL4L1, MIR221, POTEF, TGFB1, REN, SELPLG, CCL4, ATP1A3, CASP3, CRP, FN1, GDF1, GZMB, HMGB1, IFNA1, IFNA13, IFNAR1, IFNAR2, IL4, IL13, IL17A, INSRR, MMP8, NM, NOTCH1, NOTCH2, PLXNA2, PLAAT4, ADRB1, S100B, PERCC1
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Hypotonia, Hypoventilation, Impaired Intellectual Development, Dysautonomia, Epilepsy, And Eye Abnormalities
Omim
Description Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities (HIDEA) is an autosomal recessive neurodevelopmental syndrome characterized by global developmental delay, poor or absent speech, hypotonia, variable ocular movement and visual abnormalities, and respiratory difficulties, including hypoventilation, and sleep apnea. ... Rahikkala et al. (2019) reported 7 patients from 4 unrelated families with HIDEA syndrome and reviewed the large Finnish family reported by Kaasinen et al. (2014).
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Immunodeficiency 35
Omim
Clinical Features Minegishi et al. (2006) described a 22-year-old Japanese male clinically diagnosed with autosomal recessive hyper-IgE syndrome (HIES) (see 243700), a primary immunodeficiency characterized by recurrent skin abscesses, pneumonia, and highly elevated serum IgE. ... Molecular Genetics In their patient with autosomal recessive hyper-IgE syndrome and atypical mycobacteriosis, Minegishi et al. (2006) identified a homozygous deletion of GCTT at nucleotide 550 in the TYK2 gene (176941.0001), resulting in a frameshift and premature termination of the protein at amino acid 90.
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Osteofibrous Dysplasia, Susceptibility To
Omim
These examinations demonstrated the syndrome of congenital bowing of the tibia, fibular hypoplasia, and pectus excavatum transmitted as an autosomal dominant trait. ... The abbreviation OFD has the disadvantage of confusion with the several orofaciodigital syndromes, e.g., OFD1 (311200). INHERITANCE - Autosomal dominant CHEST Ribs Sternum Clavicles & Scapulae - Pectus excavatum (in some patients) SKELETAL Limbs - Lytic lesions in tibial shaft, with sclerotic border - Lytic lesions in fibular shaft, with sclerotic border - Bowing of tibia - Fibular hypoplasia (in some patients) - Pathologic fractures through sites of lytic lesions - Pseudoarthrosis of tibia - Pseudoarthrosis of fibula - Fibrous stroma with spicules of osseous trabeculae rimmed with osteoblasts on histology MISCELLANEOUS - Onset of symptoms in childhood - Spontaneous resolution of lesions during skeletal maturation - No radiologic evidence of persistent disease in adulthood MOLECULAR BASIS - Susceptibility is conferred by mutation in the MET protooncogene gene (MET, 164860.0013 ) ▲ Close
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Renal Cell Carcinoma, Papillary, 1
Omim
For background information and a discussion of genetic heterogeneity of nonpapillary renal cell carcinoma, see RCC (144700). See also a hereditary syndrome of predisposition to uterine leiomyomas and papillary renal cell carcinoma (HLRCC; 150800) caused by germline mutation in the FH gene (136850). ... The authors considered the inherited disorder in this family to be different from recognized hereditary cancer syndromes. Zbar et al. (1995) sought other families with papillary renal cell carcinoma to determine whether the large family reported by Zbar et al. (1994) represented a distinct class of inherited cancer.