- Neuromuscular Junction Disease Wikipedia
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Bruce Effect
Wikipedia
Pennsylvanicus and Peromyscus maniculatus" . Reproduction . 49 (2): 365–7. doi : 10.1530/jrf.0.0490365 .
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Carcinogenic Parasite
Wikipedia
Parasitology International . 66 (4): 365–371. doi : 10.1016/j.parint.2016.07.010 .
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Paternal Depression
Wikipedia
"Paternal depression in the postnatal period and child development: a prospective population study" . Lancet . 365 (9478): 2201–5. doi : 10.1016/S0140-6736(05)66778-5 .
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Lymphangioma
Wikipedia
"Treatment of lymphangioma circumscriptum with tunable dye laser". Cutis . 45 (5): 365–6. PMID 2357907 . ^ Patel SR, Rosenberg JB, Barmettler A (2019).
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Aromatase Deficiency
Wikipedia
Summary of known homozygous mutations in P450 arom (CPY19) gene [2] [4] [9] Gender Mutation Transcription Results Aromatase Activity (%) Female GT to GC at the 5’ Terminus of intron VI An extra 87 bp insertion, between exon VI and intron VI 0.3% Female/Male Single base change at bp 1123: C to T in exon X Cysteine being transcribed instead of Arginine at position 375 (R375C) 0.2% Female Point mutation (R457X) in exon X No Transcription - Female Mutation Valine 370 to Methionine in exon IX - - Female 1600 bp deletion in exon V Aromatase lacking 59 Amino Acids - Female Point mutation in exon X (R435C) Missense mutation that causes loss of function - Female Deletion of a single Phenylalanine residue at codon 234 in exon VI - - Female 568C insertion in CYP19A1 190 Leucine was changed to Proline - Female Single base change at bp 1094 (G to A) in exon IX Glutamine instead of Arginine being transcribed at position 365 (R365Q) 0.4 Male C-base deletion in exon V Resulting in a stop codon after 21 codons 0.0 Male C to A substitution in intron V, at 3’ splicing acceptor site before exon VI Premature stop codon - Male Insertion of 21 bp at the codon 353 in exon IX - - Male Single base change at bp 628 (G to A) in the last nucleotide of exon V Glutamic acid instead of a Lysine being transcribed at position 210 (E210K) 1.0 Table 2.
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Congenital Generalized Lipodystrophy
Wikipedia
"Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13". Nature Genetics . 28 (4): 365–370. doi : 10.1038/ng585 . PMID 11479539 .BSCL2, AGPAT2, CAV1, CAVIN1, PPARG, FOS, LMNA, ZMPSTE24, HNRNPUL2-BSCL2, LEP, KCNJ6, POLR3A, GZMH, FBN1, INSR, GARS1, AGPAT1, ADIPOQ, LPIN1, LPIN2, BEST1, SNAP23, AIFM1, ANGPTL3, SOST, SETD2, SETX, NOX1, SLC2A2, ACAT1, PLIN1, GCG, AGL, APRT, CAV3, DMD, EMD, ETFA, GART, GH1, PDE3B, GZMB, HIF1A, HNF4A, MAT1A, ADRB3, MUC1, PCYT1A, MFAP1
- Alpha-1 Antitrypsin Deficiency Wikipedia
- Monomelic Amyotrophy Wikipedia
- Akathisia Wikipedia
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Intrauterine Growth Restriction
Wikipedia
Alternative Names: Intrauterine growth retardation; IUGR ^ Lawn JE, Cousens S, Zupan J (2005). "4 million neonatal deaths: when? Where? Why?". The Lancet . 365 (9462): 891–900. doi : 10.1016/s0140-6736(05)71048-5 .ACADVL, IL1RAPL1, STAMBP, CORIN, TBR1, SIX2, CPLX1, PNPLA6, MID2, PUF60, TRAIP, CNKSR2, IQSEC2, SYNE1, OBSL1, FTSJ1, MTO1, POC1A, EMG1, COQ7, ACTB, PHOX2B, NSD2, ZNF711, ZNF41, USP9X, FZD4, TP63, MBTPS1, RECQL4, HUWE1, CRIPT, ARHGEF6, TTC37, CEP57, FRMPD4, CUL7, MED12, SIN3A, AUTS2, FBXL4, VPS13B, PPP1R15B, WDR73, CREB3L1, CCNQ, RAB39B, DNAJC21, PTCHD1, ARX, MRPS16, UBR1, FLCN, TAPT1, STOX1, PTF1A, H19, ZNF81, SLC9A7, CCDC8, ALG13, ALG12, PAM16, GMNN, SBDS, FGFRL1, NSUN2, TMEM70, PPP2R3C, TRMT1, NGLY1, MCTP2, SHROOM4, FAM111A, ZNF335, CXorf56, UPF3B, WHCR, TSHR, TSPAN7, GCK, FANCC, FANCD2, FANCE, ACSL4, FBN1, FLT1, GATA6, GDI1, IGF1, GK, GPC1, GRIN2A, GTF2E2, HADHA, HADHB, HCFC1, FANCA, ERCC6, ERCC2, EIF2S3, AGTR2, ALB, ASCL1, BUB1B, CLCN4, CNTN1, COL1A1, COL1A2, CTBP1, CYB5A, CYB5R3, DLG3, DMD, DNM2, DYRK1A, HSD11B2, IGF2, THRB, SKIV2L, PIK3R1, POR, PTS, NECTIN1, RBBP8, RET, RPS6KA3, SLC12A1, IGHMBP2, SPR, SRP54, ABCC8, SYP, TAF13, TALDO1, TGFB3, PIK3C2A, PDHA1, PAK3, ORC1, INS, INSR, PDX1, IRF6, KCNJ1, KCNJ11, LETM1, LRP5, SMAD4, MECP2, MSX1, MUSK, MYH3, NDP, NPHS1, USP27X
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Multiple System Atrophy 1, Susceptibility To
Omim
Jeon et al. (2014) did not find an association between the V393A variant in the COQ2 gene (609825.0007) and multiple system atrophy among 299 Korean patients with the disorder and 365 controls (minor allele frequency 2.7% of cases versus 2.6% of controls).
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Monoclonal Gammopathy Of Undetermined Significance
Wikipedia
"TEMPI Syndrome – A Novel Multisystem Disease" . N Engl J Med . 365 (5): 475–477. doi : 10.1056/NEJMc1106670 .TNFRSF13B, DNAH11, USP8P1, ULK4, HLA-B, SDC1, ELL2, TOM1, MAG, IL1B, IGH, NCAM1, MYOM2, CDKN2A, MYD88, HGF, CD19, IL6, STOML2, CDKN2B, CXCR4, VEGFA, IL1A, TP53, TNF, MYC, PTPRC, TTR, NRAS, PTPN6, FGF2, SOCS1, ADIPOQ, RASSF1, FOXP3, KRT20, MALAT1, HAS1, H3P10, CKS1B, CTNNB1, CD38, CCND1, MS4A1, ALB, DAPK1, GPNMB, ANP32B, COLEC10, TNFSF13B, PNMA2, NES, LILRB1, SMR3B, LRPPRC, PRSS21, ADAMTS13, PTP4A3, SERPING1, PADI2, KLRK1, BNIP3, DKK1, KDM1A, SEMA3A, CANX, RAD50, PLXNB2, TP73, CD40, VWF, NSD2, XPO1, CD34, CDR3, NR0B2, OFD1, CASK, TNFSF11, CD27, TNKS, TNFSF13, CCND3, MSC, KL, RUNX2, TBPL1, BCL2L1, SETBP1, POT1, ALKBH3, GSTK1, AKT2, MIRLET7E, MIR203A, MIR21, MIR214, MIR27B, MIR34A, MIR340, MIR342, SSX2B, MIR744, CD24, AKT1, MIR1246, KLRC4-KLRK1, PCAT1, LOC102723407, LOC102724971, RICTOR, CLEC12A, CDH1, SLCO6A1, FOXP1, IGHV3OR16-7, IGHV3-69-1, CD274, BCL2, SOST, EVL, WWOX, ALK, EGLN1, NLRP2, SLC12A9, TP73-AS1, AICDA, PREX1, IL21, IGAN1, FOXP2, EGLN3, CD47, TIMP3, DCC, IGL, HSPA5, IGSF3, IFNA2, IGF1, IGF2, IGFBP2, CCN1, CSNK1A1, IGHG3, CR2, TGFBI, COX8A, CCR7, IL6R, IL6ST, CXCL8, IL10, ITGAX, JAG2, JAK2, HRAS, CTLA4, CFH, CYLD, DKC1, EGFR, EPO, EPOR, ESR1, FAP, FCGR3A, DAP, FGFR3, FLT3, FRA16D, MTOR, FUT4, GLI1, GNA12, CXCR3, GPT, GRN, GSTP1, KIT, KRAS, LCK, PTCH1, PARP1, PVR, RALA, RPA1, CCL20, CX3CL1, CDH2, SFRP1, SFRP5, SSX1, SSX2, SSX5, SSX4, STAT3, AURKA, SYK, TRBV20OR9-2, TERF1, TERF2, CDKN1A, PFDN5, LIG3, ENPP1, LPL, LTA, LY9, CCR4, DNAJB9, MET, MGMT, MLH1, MME, MMP2, MRE11, RCBTB2, NBN, CDKN3, NEDD8, NM, PNP, NPC1, CDKN2C, ACTB
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Sudden Unexpected Death In Epilepsy
Wikipedia
"Sudden, Unexpected Death in Epilepsy". New England Journal of Medicine . 365 (19): 1801–1811. doi : 10.1056/NEJMra1010481 .
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Transneuronal Degeneration
Wikipedia
"Transneuronal degeneration in the spread of Alzheimer's disease pathology: immunohistochemical evidence for the transmission of tau hyperphosphorylation" . Neurobiology of Disease . 4 (5): 365–375. doi : 10.1006/nbdi.1997.0164 .
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Pulmonary Fibrosis
Wikipedia
"Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosis". N Engl J Med . 365 (12): 1079–1087. doi : 10.1056/nejmoa1103690 .TGFB1, CCN2, EDN1, IL1B, MMP9, NFE2L2, IL4, CCL2, IL13, TIMP1, AGT, CSF2, HPS1, FAM13A, DSP, AP3B1, ABCA3, FN1, HGF, TNF, IL6, HMGB1, TGFA, STAT3, IGF1, FGF2, CXCL8, MTOR, MMP2, SOD1, CCL11, CCR2, SERPINA1, SPP1, AREG, MIR326, ADIPOQ, HMOX1, STAT6, MIR30A, MECP2, EGF, COL3A1, MIR29C, CAT, SOD3, BMP7, FGF1, ELN, CEBPB, FGF7, CCL5, GREM1, CCL4, CCR3, PARP1, SMAD7, ACTA2, LAMB1, PDGFA, IL1RN, IL5, CSF3, MIR140, MIR125A, CYSLTR2, CEBPA, MIR26B, CMA1, FYN, MIR200C, IL12B, MIR122, MIR345, CALCA, SKIL, MIR10A, PDGFB, PTX3, SERPINE1, MIR101-1, CXCL2, MIR425, MIR378A, CCL3, CFD, EGFR, IL17A, PTGS2, AGER, COL1A1, ACE, PLAU, SMAD4, MMP1, SCGB1A1, IL1A, ELANE, CD36, TGFBR2, COL1A2, PDGFRA, CCL17, CCL22, ANXA1, HSP90AB1, CDH1, HABP2, STAT1, ICAM1, MFN2, CYSLTR1, TERT, B3GAT1, HSPD1, MUC5B, CCR4, BAD, VWF, NKX2-5, CCR8, SFTPC, MUC5AC, CAV1, HPS4, RTEL1, TERC, PARN, IRF5, SFTPA2, SFTPA1, FAM111B, HLA-DRB1, TINF2, DKC1, HLA-DPB1, CTLA4, CFTR, DCTN4, PRTN3, PRKCD, FASLG, FAS, ACTB, BTNL2, HIF1A, IL10, MRPS22, PIK3CD, PIK3CG, PIK3CB, PIK3CA, RNF168, SMAD2, NLRP3, STN1, SP110, BMP15, NHP2, HLA-DPA1, KIAA0319L, DPP9, RCBTB1, SMAD3, NOP10, NR5A1, NUP107, FSHR, THOC2, NOX4, PLEC, PSMC3IP, RASGRP1, ALMS1, ASAH1, POSTN, NKX2-1, CASP10, CLCA4, STX1A, CCR6, ATP11A, SMN2, SMN1, SPIDR, CTNNB1, PTPN22, MIR21, F2R, VEGFA, TP53, LOX, AKT1, GABPA, CXCR4, TLR4, FOSL2, PLG, COPD, ACE2, THY1, ANGPT1, TNC, SIRT3, MMRN1, GLI1, DECR1, BLM, LPAR1, CXCL12, VIM, CEL, FSTL1, LOXL2, SLC27A5, PARP9, PRKAB1, IL33, JAK2, PRKAA1, PRKAA2, TM7SF2, IFNG, MTCO2P12, SIRT1, SFTPD, COX2, LGALS3, MMP12, CCL18, MMP7, REN, S100A4, HSPA4, NR1I2, PTEN, MUC1, MIRLET7D, ZEB1, MIR34A, OGG1, ADAM17, MSC, VTN, CCN4, YY1, PPARG, SPHK1, SEMA7A, NT5E, DNM1L, SMUG1, TOP1, BRD4, SLC52A2, HSPB3, PINK1, TMED7, SPARC, PDGFRB, TGFB3, GDF15, PHEX, MAPK3, KLF4, HSP90AA1, DNER, MAPK14, MARK2, TMED7-TICAM2, F2RL1, TICAM2, BLMH, TSLP, GLB1, PWAR1, GSK3B, FOXO3, EGR1, CD44, DDIT3, DCN, DNMT1, ING4, MAPK1, ELK1, MAPK7, MAPK8, PSMD9, TLR2, LILRB1, PTK2, PTPN11, DCTN6, IL7, TSC1, CXCR6, FOLR2, PDCD1, LCLAT1, ZNRD2, FOXM1, WNT1, SLC52A1, PF4, ATF3, SSRP1, AHSA1, BDNF, STING1, UTRN, SIRT6, TXN, FASN, TWIST1, PTPRC, MIR145, HPGDS, MIR154, CD274, CST3, CHI3L1, NLRP1, CSF1R, CSF1, SLC2A1, CRYAB, CRMP1, SNAI1, CRK, SOAT1, MIR29A, SOD2, CREBBP, MIR29B1, MIR29B2, STAT4, CNR2, LTB4R, DAPK2, SDC2, SDC1, TGFBI, MOK, THBD, PRKN, METAP2, IL37, MIR155, MIR15A, MIR18A, DPP4, CX3CL1, SERPINH1, RIPK3, POLDIP2, RNF19A, TFF1, MIR200B, NUDT21, CDH11, FOS, BACH1, SOCS1, ANXA2, LGALS1, SQSTM1, JAG1, LOXL1, PERCC1, TNFSF14, HDAC4, MARCO, CTHRC1, BECN1, DENR, MIP, RBM45, HAS2, CXCL16, ANPEP, MMP13, ROCK2, LDHA, HSPB1, SETD7, S1PR2, IL9, MAPKAPK2, H3P23, CCN1, MAP1LC3B, IL18, IRAK1, HSPB2, KL, IGFBP3, GRAP2, MCU, IFI27, ITGB6, ADORA2B, LTBP4, ST2, MYD88, MPO, FST, GLI2, GPX4, P2RX7, ANXA5, TSPAN1, YAP1, CBLIF, AIMP2, GLRX, TFEB, GAS6, IL18BP, OSM, NTN1, MIR323A, RAPGEF3, MIR542, MIR1224, CHP1, TMPRSS11D, ABCG2, AIM2, GGPS1, DUSP10, TRIM16, MIR328, MIR96, LINC02605, KLF2, MIR34B, P2RX2, MIR31, MERTK, FBLN5, KAT5, CXCL13, ATG7, SLIT2, H3P11, TRIP10, MIR30D, P2RX5-TAX1BP3, ATG5, MIR541, RAMP2, ATP6AP2, MIR506, PPARGC1A, TNFSF13B, GAB2, MIR5100, MIR486-1, MIR454, MIR455, DNM3OS, CAPN9, FAM72A, NEU3, FAM72B, MIR627, HDAC6, SPATA2, RPL17-C18orf32, JTB, KHDRBS1, PLF, MIR448, PLXNC1, MIR4516, MIR449A, SIRT1-AS, CDR1-AS, PCLAF, ABCG1, H4C15, RGS6, LRPPRC, MIR503, CD226, TMX2-CTNND1, B3GAT3, ATG4B, ACKR3, TRPV4, GER, H4-16, SLCO6A1, ROMO1, TRIB3, PRX, MRTFA, RCN3, RMDN2, ASPRV1, KMT5AP1, PCBP4, TCIM, SULF1, SPHK2, RHOV, TMPRSS4, PARD3, PGAM5, MYDGF, SULF2, HDAC8, PAG1, IL26, MFN1, PRSS55, ZEB1-AS1, RXFP1, FKBP10, SCGB3A2, SMOC2, SPZ1, RETNLB, ING5, CRISPLD2, LOXL3, HAVCR2, CD276, ADAM33, WNT10A, ZC3H12A, GRHL2, NAF1, MMP28, ELOVL6, TRPM8, WNK1, CDCP1, IL25, MUC16, PRRT2, DEPTOR, NREP, SEMA4A, IFIH1, IL17F, UCN3, FBXO32, SYBU, EBF3, ELMOD2, ADGRE2, TBK1, SETD2, IL17B, BBC3, LATS2, FGF21, KISS1R, PHGDH, MIR185, PART1, MIR193A, MIR19A, MIR19B1, MIR205, MIR210, PRDX5, NUP62, MIR221, DDAH1, PIGN, MIR27A, TRAM1, MIR27B, CBX5, HEY1, PPP1R13B, MIR301A, MIR146A, DELEC1, RMDN3, MIR144, SARS2, EGLN1, ROBO4, NPNT, IFNL3, POLE3, LAMA1, PWAR4, GSTK1, SIRT7, GTSE1, MALAT1, FENDRR, SNX9, CSAD, CHST15, CRNKL1, TNFRSF12A, MIR126, MIR130A, MIR130B, MIR139, RMDN1, ADIPOR1, MIR141, MIR142, FOXP3, GORASP1, SFRP4, CRLF1, GRP, FUT8, GAB1, GATA3, GLS, CCR10, CXCR3, GPT, GTF2H1, HPGD, HDAC2, CFHR1, NRG1, HLA-A, HLA-B, HLA-C, HLF, FOSB, FLT3LG, FLT3, FLT1, ESR1, ETS2, F2, F2RL2, F3, F10, FAP, FCGR3A, FCGR3B, FGF13, FGFR2, FGL1, VEGFD, FOXF1, FOXD1, NR4A1, HSPA1A, ERN1, JUNB, ITGAE, ITGAX, ITGB3, EIF6, IVD, JAK1, JUN, JUND, HSPA1B, KCNMB1, LEP, LMNA, LRP6, LTBR, LUM, MARCKS, ITGA9, ISG20, ITGA6, INPP5D, HTR2A, ID1, IFNB1, IGF2, IGFBP2, IGFBP5, IL2, IL2RA, IL4R, IL6ST, IL7R, IL11, IL11RA, IL15, TNFRSF9, FBL, ERBB3, MEN1, CAST, KLF9, TSPO, C3, C3AR1, C5AR1, VPS51, DDR1, CASP1, CDKN2A, RUNX2, RUNX3, CBS, CD28, CD59, ADGRE5, CD151, BSG, BMPR2, BMP3, BGN, ADA, ADAM10, ADM, AEBP1, AGTR1, AIF1, AKT2, ALB, ANGPT2, ANXA11, APOA1, APRT, ARG1, BARD1, BCL2, CDH5, CDKN2B, ERBB2, E2F4, CYP27B1, DES, NQO1, DIO2, DNAH8, ARID3A, E2F1, ECE1, CHAT, ECT2, S1PR3, EFNB2, EPHA2, EIF4E, EP300, STX2, CYP2E1, CYLD, CX3CR1, CTSK, CHIT1, CHRM3, CHRNA4, CLU, ACKR2, CNR1, COL11A2, COX8A, CREB1, ATF2, CRIP1, CRYZ, CSNK1D, CSRP1, CTNND1, MCAM, MFAP1, XPR1, TNFRSF1A, TGFB2, TGFBR1, THAS, THBS1, TIAM1, TIMP3, TLR3, TNNC1, WT1, TPH1, CRISP2, TRPC6, TSC2, TNFSF4, VCAM1, VDR, TMBIM6, PPP1R11, TRBV20OR9-2, TAZ, SHH, SIX1, SKI, SKP2, SNAI2, SNCA, SOX2, SPINT1, SRC, SREBF1, SRF, STC1, STK11, SYT1, TAGLN, TRPV1, XIST, SFRP1, MBD2, AOC3, EIF3A, MBTPS1, TNFSF10, CCN6, CCN5, SGPL1, TRPA1, FOSL1, F2RL3, TM4SF5, SYT7, P2RX6, ATG12, LPAR2, IL1RL1, BHLHE40, ENC1, RASAL1, ULK1, HMGA2, H3-4, H4C9, FZD7, H4C1, H4C4, H4C6, H4C12, H4C11, H4C3, H4C8, H4C2, H4C5, H4C13, H4C14, ACO2, SELPLG, MID1, PAWR, P2RX3, P2RX4, P2RX5, P2RY1, P2RY2, P4HB, FURIN, PCNA, PIP, PDE1A, PDK1, PECAM1, ATP8B1, ABCB1, PHB, SERPINE2, P2RX1, DDR2, NTF3, NOTCH4, MAP3K11, MMP3, MMP10, MMP14, MMP19, MPG, MRC1, MSR1, MST1, NEDD8, NEU1, NFKB1, NINJ1, NM, NOTCH1, PIN1, PLA2G4A, SELE, ROCK1, RASA1, RBP2, OPN1LW, RELA, RGS2, BRD2, RNH1, ROS1, PLAUR, RPL17, S100A6, S100A9, SARS1, SERPINB3, CCL24, SDC4, RARRES2, RAG2, RAF1, RAC2, PLK1, POU2AF1, PPL, PRH1, PRH2, PRKCA, PRKCB, PRKDC, EIF2AK2, PTCH1, PTGER4, PTHLH, PTPN13, PTPRJ, RAC1, H3P10
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Eclabium
Wikipedia
"Types of congenital nonsyndromic ichthyoses" . Biomedical Papers . 164 (4): 357–365. doi : 10.5507/bp.2020.050 . 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 Category:Lip disorders
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Arachnoid Cyst
Wikipedia
"Haemorrhage into an arachnoid cyst: a serious complication of minor head trauma" . Emerg Med J . 19 (4): 365–6. doi : 10.1136/emj.19.4.365 . PMC 1725893 .
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