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Oligohydramnios
Wikipedia
CS1 maint: DOI inactive as of December 2020 ( link ) ^ Johnson JM, Chauhan SP, Ennen CS, Niederhauser A, Magann EF (2007). "A comparison of 3 criteria of oligohydramnios in identifying peripartum complications: a secondary analysis". ... Gynecol . 197 (2): 207.e1–7, discussion 207.e7–8. doi : 10.1016/j.ajog.2007.04.048 .PDGFB, PDGFRA, PDGFRB, PDGFA, PDPN, HYMAI, PIGV, OSGEP, WNT4, CEP55, RFWD3, FANCL, TMEM70, MKS1, BNC2, MAGEL2, FANCI, AGT, MBTPS2, WDPCP, DONSON, SLC25A24, GMPPB, UBE2T, PGAP2, COQ2, INVS, B9D1, NPHP3, FGF20, TCTN3, LARS2, TMEM216, RPGRIP1, RPGRIP1L, BRIP1, PIGW, NEK8, NALCN, EBF3, BMPER, AMER1, PGAP3, NEK9, TMEM67, PIGY, WDR73, PIGO, SLX4, TMEM107, B9D2, PDSS2, CEP290, GREB1L, TCTN2, CSPP1, TXNDC15, PALB2, DYNC2H1, TMEM231, ALG8, ALX4, FANCM, DOCK6, CC2D2A, ERGIC1, ADNP, POMT1, PUF60, LIFR, HSPA9, HBA2, HBA1, GLI3, GCDH, GATA6, FBN1, FANCG, FANCF, FANCB, FANCE, FANCD2, FANCC, FANCA, ERCC4, DHPS, DHCR7, ACE, CHRM3, C1QBP, BUB1B, BRCA2, BRCA1, ATRX, ATP5F1D, ASCL1, ALB, LHX1, MYH3, AGTR1, OPHN1, FBLN5, COG5, MAD2L2, COQ7, CERT1, FARSB, KIF14, SEC24D, PIGL, TRIP4, PHOX2B, ITGA8, ARID1A, XRCC2, UBE2A, HNF1B, TALDO1, SLC20A2, RET, REN, RAD51C, RAD51, POR, EXOSC9, PLAGL1, PKHD1, PBX1, RNU4ATAC
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Hughes–stovin Syndrome
Wikipedia
The syndrome is also identified as being "characterized by pulmonary/bronchial artery aneurysms and thrombophlebitis, without diagnostic features of Behçet's disease (BD)." [4] Management [ edit ] There is currently no satisfactory treatment for this condition. [4] This is partly due to its rarity; the Orphanet Journal of Rare Diseases claims that fewer than forty cases of the disease have been described in English medical literature. [5] Immunosuppressive therapy is the most common treatment, involving a mix of glucocorticoids and cyclophosphamide . ... "Hughes-Stovin Syndrome: a case report and review of the literature" . Cases J . 2 : 98. doi : 10.1186/1757-1626-2-98 . PMC 2649053 .
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Tethered Spinal Cord Syndrome
Wikipedia
Please help improve this article by adding citations to reliable sources . ... Thieme Medical Publishers, Inc. p. 90. ISBN 978-1-60406-241-0 . The diagnosis of TCS is primarily based on neurological and musculoskeletal signs and symptoms. ... "Pediatric urodynamics: basic concepts for the neurosurgeon" . Neurosurg Focus . 23 (2): E8. doi : 10.3171/FOC-07/08/E8 . PMID 17961012 . ^ Hadley, H. ... "Management of Recurrent Adult Tethered Cord Syndrome". Neurosurgical Focus . 29 (1): E5. doi : 10.3171/2010.3.FOCUS1073 .MTHFR, PAX3, PDGFRA, VANGL2, PCMT1, CFL1, PON1, CHKA, CCL2, TXN2, PCYT1A, FGFR2, RNF2, SUZ12, MTRR, MTR, MTHFD1, BRCA1, SLC25A1, PTCH1, DLL4, FLI1, FANCL, RFWD3, FANCI, TRIM36, FANCC, SUFU, PSAT1, UBE2T, PHGDH, FANCF, HAAO, MEOX1, PTCH2, MAD2L2, LMX1B, RBM8A, BMS1, KIF22, FANCG, GDF3, FANCB, CREBBP, BRIP1, BRCA2, RAD51C, SLX4, RAD51, PALB2, FANCE, RMRP, PORCN, XRCC2, GDF6, SLC25A19, FANCM, ERCC4, FANCA, FANCD2, ZIC2, DHFR, GRHL3, FUZ, BHMT, CELSR1, TYMS, PTK7, CBS, NOS3, LEPR, NAT1, PAX1, PRCP, SLC19A1, TIMP2, CYP26A1, GRHL2, CBSL, AFP, PGPEP1, FOLR1, FOLR2, SCRIB, COMT, BMP1, ZIC1, VSIR, PKD2L1, VANGL1, ANKEF1, CD200R1, PRICKLE2, UCP2, PCSK9, TP53, SLC5A11, SLC39A4, CCDC88A, ALDH1A2, ISYNA1, TGIF1, TRIM26, FZD3, FKBP8, BHMT2, GPR161, CUBN, DVL1P1, FOXN1, ALDH1L1, MTHFD2, TNIP1, NKX2-8, NNMT, TGFB1, SOX3, GCKR, FOSB, FOS, FOLH1, FLT4, GPC5, FGF3, FAP, ERCC2, EPHA4, DVL3, DVL1, DPP4, TRDMT1, SARDH, CSF2, CRABP2, ABCC2, CD38, CASP8, CASP3, BMP4, BDNF, ARSA, APOE, APOB, APEX1, APAF1, ABO, GLI2, GNAS, UTS2R, LAMC2, SLC2A1, SKI, RFC1, PRKCB, PRKCA, NAT2, NGF, MS, CD200, MMP2, LRP6, LMNB1, LEP, JUND, HK1, JUNB, JUN, JARID2, ITPK1, IL18, IL13, IL10, HOXD@, HOXC@, HOXB@, HOXA@, HMOX1, HLA-DRB4, RN7SL263P
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Haemophilus Meningitis
Wikipedia
A child in the presence of family members sick with Haemophilus meningitis or carrying the bacteria is 585 times more likely to catch Haemophilus meningitis. [6] Additionally, siblings of individuals with the Haemophilus influenzae meningitis receive reduced benefits from certain types of immunization. [7] Similarly, children under two years of age have a greater risk of contracting the disease when attending day care, especially in their first month of attendance, due to the maintained contact with other children who might be asymptomatic carriers of the Hib bacteria. [3] Diagnosis [ edit ] This section is empty. You can help by adding to it . ( February 2019 ) Prevention [ edit ] Before the widespread use of the Hib vaccine, Haemophilus meningitis accounted for 40%-60% of all meningitis cases in children under the age of fifteen, and 90% of all meningitis cases in children under the age of five. [3] Vaccination can reduce incidence. [8] Vaccination has reduced the occurrences of Haemophilus meningitis by 87-90% in countries with widespread access to the Hib vaccine. [3] Rates are still high in areas with limited levels of vaccination. [9] Less-developed countries as well as countries with medical infrastructure that has been damaged in any way, such as from warfare, do not have such widespread access to the vaccine and thus experience higher rates of meningitis cases. ... Retrieved 30 October 2014 . ^ Ward JI, Fraser DW, Baraff LJ, Plikaytis BD (July 1979). "Haemophilus influenzae meningitis. ... "Siblings of patients with Haemophilus meningitis have impaired anticapsular antibody responses to Haemophilus vaccine". J. Pediatr . 103 (2): 185–91. doi : 10.1016/s0022-3476(83)80342-4 .
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Molybdenum Cofactor Deficiency
Wikipedia
Nucleosides, Nucleotides & Nucleic Acids . 25 (9–11): 1087–91. doi : 10.1080/15257770600894022 . ... Retrieved May 13, 2010 . [ dead link ] External links [ edit ] Classification D ICD - 10 : E72.1 OMIM : 252150 DiseasesDB : 29821 External resources eMedicine : ped/2172 Orphanet : 99732 v t e Metabolic disorders of vitamins , coenzymes, and cofactors B7 Biotin / MCD Biotinidase deficiency Holocarboxylase synthetase deficiency Other B B5 ( Pantothenate kinase-associated neurodegeneration ) B12 ( Methylmalonic acidemia ) Other vitamin Familial isolated vitamin E deficiency Nonvitamin cofactor Tetrahydrobiopterin deficiency Molybdenum cofactor deficiency
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Superior Mesenteric Artery Syndrome
Wikipedia
While research establishing an official mortality rate may not exist, two recent studies of SMA syndrome patients, one published in 2006 looking at 22 cases [11] and one in 2012 looking at 80 cases, [17] show mortality rates of 0% [11] and 6.3%, [17] respectively. ... "Late superior mesenteric artery syndrome in paraplegia: case report and review" . Spinal Cord . 40 (2): 88–91. doi : 10.1038/sj.sc.3101255 . PMID 11926421 . ^ Barsoum, M. ... Journal of Pediatric Surgery . 42 (10): e5–e8. doi : 10.1016/j.jpedsurg.2007.07.002 . ... "Superior mesenteric artery syndrome: an uncommon cause of intestinal obstruction". South. Med. J . 93 (6): 606–8. doi : 10.1097/00007611-200006000-00014 .
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Border Disease
Wikipedia
Viral disease of sheep and goats caused by Pestivirus D Pestivirus D Virus classification (unranked): Virus Realm : Riboviria Kingdom: Orthornavirae Phylum: Kitrinoviricota Class: Flasuviricetes Order: Amarillovirales Family: Flaviviridae Genus: Pestivirus Species: Pestivirus D Synonyms . [1] Border disease virus Border disease ( BD ) is a viral disease of sheep and goats , primarily causing congenital diseases, but can also cause acute and persistent infections. It first appeared in the border regions of England and Wales in 1959, and has since spread world-wide. Lambs that are born with BD are commonly known as 'hairy shakers' due to the primary presentation of the disease. ... A slight fever and a mild leukopenia may be seen with a short-lived viremia , detectable between days 4-11 post infection, at which point the virus is neutralized by the animal's immune system. [6] Fetal infection [ edit ] While the level of evident maternal infection may be minimal, the consequences for the fetus are serious before day 85 of gestation . After day 85, the lamb is most likely to be born normal with antibodies to the virus, given the state of the fetal immune system at this stage in gestation. ... The 'hairy shakers' are born with hair (not wool) and the shaking comes from cerebellar hypoplasia. [5] Persistent viraemia [ edit ] Feti that are infected between 60–85 days of gestation have a 50% chance of survival.
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Placental Insufficiency
Wikipedia
. ^ McCormack, RA; Doherty, DA; Magann, EF; Hutchinson, M; Newnham, JP (October 2008). ... British Journal of Obstetrics and Gynaecology . 84 (9): 656–63. doi : 10.1111/j.1471-0528.1977.tb12676.x . ... British Journal of Obstetrics and Gynaecology . 98 (11): 1163–7. doi : 10.1111/j.1471-0528.1991.tb15371.x . ... Archives of Disease in Childhood: Fetal and Neonatal Edition . 84 (2): F96–F100. doi : 10.1136/fn.84.2.f96 . ... American Journal of Obstetrics and Gynecology . 177 (5): 1079–84. doi : 10.1016/s0002-9378(97)70018-8 .
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Pilon Fracture
Wikipedia
"Decisions and staging leading to definitive open management of pilon fractures: where have we come from and where are we now?". J Orthop Trauma . 26 (8): 488–98. doi : 10.1097/BOT.0b013e31822fbdbe . PMID 22357091 . ^ Crist, BD; Khazzam, M; Murtha, YM; Della Rocca, GJ (Oct 2011). ... Journal of Orthopaedics, Trauma and Rehabilitation . 24 : 84–89. doi : 10.1016/j.jotr.2017.08.001 . ^ Jacob N, Amin A, Giotakis N, Narayan B, Nayagam S, Trompeter AJ (November 2015). ... "Tibial pilon fractures: which method of treatment?". Injury . 41 (11): 1183–90. doi : 10.1016/j.injury.2010.08.041 .
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Bird Fancier's Lung
Wikipedia
See also [ edit ] Hypersensitivity pneumonitis Farmer's lung References [ edit ] ^ Hashisako, Mikiko; Fukuoka, Junya; Smith, Maxwell L. (2018), "Chronic Diffuse Lung Diseases", Practical Pulmonary Pathology: A Diagnostic Approach , Elsevier, pp. 227–298.e5, doi : 10.1016/b978-0-323-44284-8.00008-9 , ISBN 9780323442848 ^ King, Thomas C. (2007), "Respiratory Tract and Pleura", Elsevier's Integrated Pathology , Elsevier, pp. 197–216, doi : 10.1016/b978-0-323-04328-1.50014-0 , ISBN 9780323043281 ^ King, Thomas C. (2007), "Respiratory Tract and Pleura", Elsevier's Integrated Pathology , Elsevier, pp. 197–216, doi : 10.1016/b978-0-323-04328-1.50014-0 , ISBN 9780323043281 ^ King, Thomas C. (2007), "Respiratory Tract and Pleura", Elsevier's Integrated Pathology , Elsevier, pp. 197–216, doi : 10.1016/b978-0-323-04328-1.50014-0 , ISBN 9780323043281 Hargreave FE, Pepys J, Longbottom JL, Wraith DG (1966).
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Hypertension
Wikipedia
A chest X-ray or an echocardiogram may also be performed to look for signs of heart enlargement or damage to the heart. [23] Classification in adults [ edit ] Classification in adults (Persons with systolic and diastolic in different categories are assigned to the higher category. [7] ) Category Systolic , mmHg Diastolic , mmHg Hypotension < 90 < 60 Normal 90–119 [7] 90–129 [83] 60–79 [7] 60–84 [83] Prehypertension (high normal, elevated [7] ) 120–129 [7] 130–139 [83] [84] 60–79 [7] 85–89 [83] [84] Stage 1 hypertension 130-139 [7] 140–159 [83] 80-89 [7] 90–99 [83] Stage 2 hypertension >140 [7] 160–179 [83] >90 [7] 100–109 [83] Hypertensive crises ≥ 180 [7] ≥ 120 [7] Isolated systolic hypertension ≥ 140 [7] < 90 [7] Isolated diastolic hypertension [85] [86] < 140 ≥ 90 In people aged 18 years or older hypertension is defined as either a systolic or a diastolic blood pressure measurement consistently higher than an accepted normal value (this is above 129 or 139 mmHg systolic, 89 mmHg diastolic depending on the guideline). [5] [7] Other thresholds are used (135 mmHg systolic or 85 mmHg diastolic) if measurements are derived from 24-hour ambulatory or home monitoring. [73] Recent international hypertension guidelines have also created categories below the hypertensive range to indicate a continuum of risk with higher blood pressures in the normal range. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure (JNC7) published in 2003 [27] uses the term prehypertension for blood pressure in the range 120–139 mmHg systolic or 80–89 mmHg diastolic, while European Society of Hypertension Guidelines (2007) [87] and British Hypertension Society (BHS) IV (2004) [88] use optimal, normal and high normal categories to subdivide pressures below 140 mmHg systolic and 90 mmHg diastolic. ... Hypertension is classified as "resistant" if medications do not reduce blood pressure to normal levels. [27] In November 2017, the American Heart Association and American College of Cardiology published a joint guideline which updates the recommendations of the JNC7 report. [89] The 2020 International Society of Hypertension guidelines define hypertension based on office blood pressure ≥140/90 mmHg or home monitoring blood pressure ≥135/85 mmHg, or 24-hour ambulatory blood pressure average ≥130/80 mmHg (daytime average ≥135/85 mmHg or nighttime average BP ≥120/70 mmHg). [90] Children [ edit ] Hypertension occurs in around 0.2 to 3% of newborns; however, blood pressure is not measured routinely in healthy newborns. [33] Hypertension is more common in high risk newborns. ... High blood pressure must be confirmed on repeated visits however before characterizing a child as having hypertension. [91] Prehypertension in children has been defined as average systolic or diastolic blood pressure that is greater than or equal to the 90th percentile, but less than the 95th percentile. [91] In adolescents, it has been proposed that hypertension and pre-hypertension are diagnosed and classified using the same criteria as in adults. [91] The value of routine screening for hypertension in children over the age of 3 years is debated. [92] [93] In 2004 the National High Blood Pressure Education Program recommended that children aged 3 years and older have blood pressure measurement at least once at every health care visit [91] and the National Heart, Lung, and Blood Institute and American Academy of Pediatrics made a similar recommendation. [94] However, the American Academy of Family Physicians [95] supports the view of the U.S. ... Annals of Internal Medicine . 162 (3): 184–91. doi : 10.7326/M14-0773 . PMID 25531552 .PPARG, APOA1, HSD11B2, MMP2, NOS3, ATP2B1, APOE, NR3C1, ECE1, GJA1, HIF1A, IL1B, CAV1, CAT, CYBA, AVP, NOX4, NOS2, CCL2, AGT, NPPB, ADRB1, REN, RGS2, AGTR2, KLK1, NPPA, NPR1, TNF, ADD1, CD36, MMP9, CRP, ACE, ACE2, TGFB1, LEP, IGF1, CYBB, EDNRA, PTGS2, EDN1, HMOX1, SERPINE1, AGTR1, UCP2, VWF, TH, UTS2, INS, HP, BDKRB2, PPARA, SOD1, GLP1R, ATP1A1, RGS5, AR, KCNMB1, SOD3, SOD2, SLC12A2, TRH, AQP1, GRK2, GJA5, TIMP1, OLR1, MTOR, VCAM1, BCL2, GPX1, ADRA2A, RELA, JUN, GSK3B, FOS, GAL, PRKCD, ADCY5, IKBKB, WNK1, WNK4, OXT, ATP1A2, ELN, HRH3, SCNN1B, SCNN1G, UMOD, ANXA1, SLC9A3R2, SCNN1A, TP53, GNAS, GUCY1A1, GCH1, CBS, FN1, COL3A1, PTH, POMC, COL1A1, GSTT1, TLR4, EPO, GNB3, CALCA, LPL, NEDD4L, SLC12A3, F12, VDR, CYP1A1, CYP11B1, ADIPOQ, KNG1, IL6, ALB, LEPR, STK39, GCG, ENG, HSD11B1, PLAT, ICAM1, FBN1, LOX, SELP, DRD2, SLC6A2, CCN2, AHR, EGFR, PLG, THBD, NCF1, C3, PRKG1, OXSR1, SH2B3, CXCR2, INPPL1, TRPC3, ERAP1, CMA1, ORAI1, PTPN1, CACNA1C, CLCNKA, GJA4, TGM2, CETP, AOC3, ALOX15, SLC6A18, STIM1, GCLC, TACR1, GSTP1, CRHR2, HTR2B, ALAD, VAV3, PTEN, DUSP5, KCNJ1, F11, IER3, MYO6, TRPC5, STK11, AOC1, UCN, ATP2B3, PROC, RPS6KB1, ITM2B, CELA2A, CHGA, CACNA2D1, NPTN, RALBP1, PPBP, GSTM1, NPY, ADRB2, ADRA2B, ADRA1A, GJC1, GSTT2, ADM, EDN3, CXCL2, ESR2, ATP6AP2, SLC9A3, MME, MYH7, MDH1, GNRH1, TPM1, APLN, FXYD2, LGALS3, ABCC1, CYP4A11, MYD88, GSTA5, ATOX1, REG3G, KL, LHB, MC2R, SLC5A2, NFE2L2, LTF, IL10, GP1BA, KDR, AGER, XDH, F3, MAS1, EDNRB, ARG1, CYP19A1, PNMT, NOS1, SLC8A1, CLOCK, AKT1, GSTM2, ACSM3, COMT, CHI3L1, IL1RN, DBH, MFN2, F11R, UTS2R, KCNQ1, APP, ADD2, AVPR1A, EPHX2, KCNA5, MMP7, CCR5, FADS1, HAVCR1, CDKN2A, SST, HDAC6, RAG1, SLC2A1, ALOX5, ADA, AQP2, FGF2, BDKRB1, ARG2, ARID1B, HSPD1, BECN1, EGLN1, NQO1, CRHR1, CNR1, ADAMTS16, BAX, MIF, CASP3, PDGFRB, AKT2, GNAI2, MAPK8, HTR1B, PRKCA, PTK2B, SRF, KYNU, CPS1, GRK5, AGTRAP, SLC6A3, CCL28, KCNJ11, TAC3, YWHAZ, HDAC8, SLC4A4, HSD3B1, TRHR, STS, UCP3, LRP2, CYP11A1, RHOA, NCF2, CTSC, ALOX12, NPY1R, SLC6A19, PLCD1, PRKCB, POSTN, CYP4F12, PDGFRA, IGF1R, RAMP2, F2R, SLC9A3R1, S1PR1, ABCC9, OPA1, IGFBP2, NISCH, NGF, LIPG, F7, KCNJ8, CLDN16, ENO1, ITGAV, KCNAB1, ATG7, CYP11B2, CYP17A1, ABAT, CORIN, AQP4, MTPN, HSPG2, CUL3, APOB, DUSP1, RFFL, DRD3, ACTC1, DYNLL1, TJP2, HSD17B4, CYP4A22, CD82, SQSTM1, FADD, GRK3, ADD3, GABBR1, ADORA1, RESP18, BAD, GNAI3, TNFRSF11B, ARHGDIA, H2AX, SLC2A3, NFKBIA, NGFR, KLHL3, RNPEP, RGS4, MAP1LC3A, CASP8, CASP9, RAD51, ATF2, OXTR, QDPR, PTPRJ, CCNE1, PTK2, PDGFB, ENTPD2, SERPINE2, PIK3R1, PKD1, PRKCE, MYOD1, COX5B, NR3C2, TACR3, FAH, ARRB2, HSD3B2, EP300, MC4R, ATP2A3, ATP5F1A, AVPR2, CDO1, NR2F2, TBXAS1, EIF4G2, MSX2, NUDT1, MYH9, SRC, COX2, BMPR2, BRCA1, KCNK3, LDLR, KCNJ5, ENPEP, PKD2, NOTCH3, FLT1, ACVRL1, PDE3A, FGF5, HFE, CACNB2, CFH, COX1, TGFBR2, JAK2, TRPC6, CDKN2B-AS1, ABCB6, ABCC6, CASZ1, STOX1, ENPP1, CACNA1H, PCSK9, ARHGAP42, LMNA, SMAD3, NT5C2, CFHR3, CCND1, SERPINA6, LYZ, CTLA4, ARMC5, PKHD1, FMR1, TET2, NOTCH1, NF1, MYH11, ANTXR2, B2M, FOXF1, MGP, TGFBR1, ALMS1, VHL, WT1, FMO3, CNNM2, ULK4, MKKS, GLA, PGPEP1, TGFBR3, RBM47, PLCE1, NFU1, TNFRSF11A, NOD2, TGFB3, TBX2, KRT8, SMAD6, CD46, MEF2A, HMBS, MOV10, L3MBTL4, ND1, MTTP, CFHR1, MYLK, ANGPTL6, FURIN, PLIN1, PMM2, PRKACA, PRTN3, ABCG8, IFIH1, GATA5, ATXN2, GRK6, RPTOR, H19, CD2AP, FGA, CYP21A2, CACNA1D, ACAT1, NKX2-5, CLCN2, ACTN4, COL4A1, CALR, BRCA2, CPOX, SRGAP3, OFD1, SESN2, MIR21, LRIG2, OR5B12, PDE11A, FGD4, BORCS7, TTC8, ADRB3, SLC25A11, DNAAF1, GPR101, ZNF831, ITGA8, PLEKHG1, ELP1, DBP, AGAP1, COL4A3, ZNF536, PAM16, BNC2, PDE8B, CRIP3, RAPGEF5, LRRC10B, PSTK, DECR1, APOL1, EML6, VANGL1, BMS1, CYP4F2, ARL6, BBS5, DIS3L2, PDE5A, MACROD2, STN1, EDA, PIK3CG, SMARCAL1, ERCC8, TRIM28, ND5, COQ7, SUGCT, MICALL2, XRCC4, ZMPSTE24, CFI, IDUA, DARS2, BBS10, ABCB1, PGF, LINC02875, SLC2A10, TMEM212, MKS1, INSR, MAFB, DPEP1, PLEKHH2, FAM131A, MFAP5, CEP290, IL17A, FGF23, TMEM70, BAG6, DPP4, FUZ, SGCZ, KRT18, WDPCP, COL4A4, COL4A5, TRNQ, TRNS1, TRNS2, SLC33A1, DNAJB11, TRNV, TRNW, MUC1, TAF1C, SELENBP1, P4HA2, TRIP13, SLC52A3, ALDH2, PHF21A, PGR-AS1, MYO9B, DYRK1B, ADA2, BBIP1, TMEM67, ND6, MTHFR, CYTB, COX3, TRNE, AIP, TRNC, TRNF, MMP14, TRNH, CST3, USP8, CERS5, TRNK, MPL, TRNL1, CEP19, BORCS7-ASMT, NLRP3, COL5A1, LPA, LZTFL1, LMX1B, CYP2J2, COL5A2, CYP3A4, NOTCH2, HOTTIP, ANGPT2, CYP3A5, MLXIPL, KLK4, NPHP1, TUBB6, IQCB1, PRRX1, BANF1, LRP6, NDUFS3, SMAD4, MAT2A, TARID, APLNR, ZDHHC2, KLHL29, NFATC2, NFIX, CYP2B6, PTPMT1, ADAMTSL4, CYP2C19, LYN, ANGPT1, APBB1IP, CCHCR1, LSP1, WRN, YES1, WNT2B, ERCC4, MTCO2P12, BBS2, GRK4, GPR39, CDH23, BBS4, GPR20, PTPN22, SWAP70, KIF1B, IFT172, ALX4, CAD, HPSE2, NSMCE2, HOXA-AS2, TRAF3IP1, GPT, TRIM32, SLC39A8, POU6F2, REST, ACACA, CAPZA1, ERCC6, BSCL2, TGFB2, ESR1, ABCG5, EIF4BP8, BBS1, CEP164, PON1, RNU1-4, EXT2, F2, FGF21, GML, LDLRAP1, EDA2R, LRRC7, G6PC, ZNF318, FRMD3, SLC12A1, BST1, KCTD1, ZFAT, COPD, SLC37A4, CC2D2A, NPHP4, WDR35, LEMD3, FOXE3, ARHGAP31, HECTD4, LINC00862, RGL3, GPC3, GH1, TRPV4, FES, VPS51, CFB, CUX2, RPGRIP1L, STK3, SGK1, FGFR2, LARS2, SHBG, RETN, SIRT1, SLC12A9, GBA, WDR19, NPHP3, HSPB8, ND4, HOXA3, BBS9, HLA-DPA1, HLA-DPB1, SLC22A7, CCDC28B, SDCCAG8, TM7SF2, HMGCS2, CDH18, PRKAR1A, ACTA2, PTPN11, C8orf37, TNXB, BBS12, TMEM237, PTGIS, HOXB7, HOXA11, FGD5, ATM, YY1AP1, TLR1, HBB, THPO, OSGEP, BBS7, IKZF5, INF2, POR, IFT27, RARRES2, INVS, POU3F4, AFG3L2, HGD, SLC52A2, VEGFA, ACTB, PPARGC1A, CLDN19, SPP1, FTO, CSK, CTNNB1, NOX1, HCRT, LCN2, HGF, GDF15, GSTK1, RNLS, DDAH1, CYP2C9, GABPA, PTX3, CSF2, F5, SLCO6A1, PIK3CD, GPR42, CABIN1, MAT2B, HSPA4, LPAR2, MMP3, PIK3CB, ACKR3, ANO1, CASR, PIK3CA, IL1A, RAC1, BEST1, HMGB1, NPR3, BDNF, BRS3, CLCNKB, THBS1, CXCR6, TXNRD3, MAPK3, LAMC2, EPAS1, SGSM3, SIRT3, PPIG, FAAH, IFNG, SSTR4, ARTN, TLR2, TRPV1, CD34, MOK, PITX2, ROS1, APRT, APOC3, BMP4, STAT3, SLC26A4, KLK3, PTGS1, ADAM17, PDC, SPHK1, MIR155, OR10A4, IRS1, SETD2, ROCK2, GPER1, MFAP1, AGRP, HPGDS, OSR1, IL18, DRD1, COL18A1, TNFRSF1B, ACR, MAPK1, CD59, CHDH, STK24, CYP2D6, ANPEP, ARSA, PPIA, MIR214, MIR29B1, APOA5, CHST3, MIR29A, P2RX7, DYM, ADORA2B, MIR204, IL4, CXCL8, ADRA1D, EGF, MIR145, MLC1, CRH, EMILIN1, RBP4, MTRR, SELPLG, TAC1, CYP1B1, CYP1A2, HDLBP, SELE, DUOX2, FAS, LOC102724197, PER1, ADM2, CX3CL1, MIR223, SLBP, SLC6A4, GCK, BTBD8, IGF2, SLC7A1, G6PD, GPR151, PPARGC1B, PLA2G7, MRGPRX1, LPAR3, SERPINA5, DAPK2, CCR2, KLF15, STAM2, MIR29B2, HLA-B, FLNA, CAST, ATP5PF, OXER1, OGA, AZU1, HEBP1, EIF2AK4, VN1R17P, S100A6, PRKAA2, RAMP1, S100A12, TRPM8, CRY2, TOR2A, PHACTR1, GPR166P, SCN10A, HTR2A, LGR6, GPRC6A, TLR3, PRKD1, ND2, FZD4, MRGPRX4, PIEZO1, MINDY4, KCNMA1, DUOX1, DAPK3, APEX1, CTH, CRY1, MRGPRX3, GAL3ST1, PTGES, AFP, CYP2C18, MYOCD, DLD, GGTLC1, PAH, HAP1, MIR146A, MBD2, CD44, UCP1, TXN, CD40LG, SULT1E1, ABCA1, TSC1, CX3CR1, ISYNA1, C5AR1, SERPINA3, PSMD9, MMP1, MAPK9, CLIC4, GGT1, NR1I2, S100A4, ROCK1, SUCNR1, SHMT1, SLC4A5, GDF2, CDH13, RYR2, PRKAB1, LIPC, PRKAA1, FGF1, ARHGEF40, CRK, DDR1, MIR130A, CAPN10, FABP3, FASN, BTN2A1, MBL2, BCHE, ACCS, CST12P, COX8A, FABP2, GRAP2, ASIC1, POLDIP2, BMP10, JAG1, CYP2C8, MIR17, IL33, CRMP1, VNN1, TNNI3, SLC9C1, UTRN, CD14, INSRR, FGB, TBX4, CXCL12, ATP1B1, ACSS2, AHSA1, CENPJ, PRCP, DDAH2, PADI4, MAPK14, EHMT1, BSND, PHA2A, SLPI, DENR, AIMP2, HNP1, EDN2, SLC9A1, PLA2G15, DNM1L, MALAT1, CLU, ADCYAP1, SESTD1, DMD, PHEX, SLC25A3, PFN1, PDE4D, JPH3, CNN1, PARP1, PECAM1, DIO2, TESC, P2RX3, MIR143, NUCB2, MPO, ITGB2, IAPP, SLC2A5, SLC35A1, DNMT1, SIK1, ADIPOR1, MPI, RNF19A, HTN3, VEGFC, VIP, EGR1, LBP, LAD1, CIMT, TNC, YAP1, PART1, SERPINF2, FOXO1, SLC5A4, RNF213, ADRA2C, CMKLR1, COMMD5, DHX40, ID2, HDAC9, MIR424, SMUG1, SULF2, USE1, HNF1A, SNAI1, AKR1B1, ZC3HC1, CLTRN, BCL2A1, SRM, ST2, BGLAP, ABCC8, POU2F3, TXN2, NOG, ULK3, SIRT6, NNT, PRDX2, DST, MIR518C, TBX1, SERPINA7, BMP2, ATP2B2, SV2C, IGF2BP2, TMED7-TICAM2, GGT2, GGTLC3, CPQ, WNT5A, GNA14, APC, VCL, SORBS1, UGT1A1, UQCRFS1, SLCO1B1, PDLIM5, GOSR2, ANXA5, SCGB1A1, ARSD, CD274, CNBP, PXDN, RHOBTB1, HBHR, FOXP3, ADRA1B, NR4A3, IL22, NOX3, ZGLP1, TMED7, GGTLC4P, TRPM7, ADORA2A, ADH1B, DEGS1, TUG1, CXCR4, NAMPT, SLC4A7, TWIST1, TFAM, TTR, MCM3AP, ALDH7A1, THBS4, B3GAT1, RN7SL263P, ATR, AKAP10, AMH, ABO, GPR182, SLC17A5, TGFA, MMRN1, SEPHS1, ERAL1, DKK1, FBXO8, ADAMTS13, SDS, C1QL1, TPT1, IMPACT, TSHR, TRPM2, GGTLC5P, SERPINC1, EBP, CRISP2, ATP2A2, MIR510, FOXRED1, NFAT5, NES, ANGPTL3, TNFRSF1A, TMSB4X, ABCG2, ARNTL, NECTIN1, PLN, MIR142, PRSS8, CD40, NLRC3, IL16, PRL, PRKCH, HBG2, HCRTR1, CD68, CD69, SLC9B2, ELK3, MS, PPP3R1, ARID3A, PTPA, TICAM2, ENTPD1, PSEN1, FSD1, ZBTB7C, AGXT2, CD5L, CD28, IFNB1, ETS1, PTGER4, PTGER1, PTGDS, COL17A1, FBL, ELANE, SETD3, PRSS55, BPIFB4, UBE2Z, CD38, FNDC1, NFYA, SMARCA4, ETV3, MIR23A, SERPINB2, PLEKHA7, SPZ1, MIR150, MIR221, CPB2, PEAR1, MIR22, TLX2, CCNL2, PDK1, CLCN6, NEFH, PDE3B, HPT, RETNLB, PCSK1, EPHB1, MIR25, NOX5, MIR26B, CDK6, SLC29A1, CDKN1A, NRG1, PPARD, EPHB6, FSD1L, EPHB2, HT, P2RY6, HLA-DRB1, PCSK6, MIR27B, PLXNA2, LRPAP1, MIR27A, PAEP, NFIL3, GSTM3, CCL5, SCT, SLC2A2, LGALS2, SHC1, HJV, IDE, SFTPC, SFRP5, GATA4, GCGR, GDNF, SDHB, SCPEP1, CCL21, GEM, GFAP, NPPC, CTSB, MAP6, SLC2A4, NPNT, HCCAT5, SLC22A2, SEMA6A, LRP1, BSG, BTF3P11, CYP4F3, SMAD2, FOSL2, MAOB, LIPA, FSHMD1A, TRIB3, FSHR, ARHGEF25, C1QTNF1, SLC3A1, GHRH, NPL, GHSR, FBRS, CAPN1, KCNJ13, GPR35, DHFR, RFC1, CYB5R3, RENBP, NTS, EFNB3, SLC39A12, OPN1LW, RCN2, CSMD1, GRN, CXCL1, GSR, MIR34A, OGG1, MIR192, DCN, NT5E, MIR126, LCT, IGAN1, SAI1, CTSL, KLKB1, RYR3, RYR1, MDK, LINC01194, GOLPH3, EFEMP1, GNA12, FABP1, CBLN2, SIK1B, SENP1, PADI1, CD300LG, APCDD1, TRPM5, GRHL1, GNPDA2, PSAT1, TDRD9, SLC26A9, MIR107, SLC22A12, MIR103A2, MIR100, MRPL4, ATL1, MIRLET7B, FIS1, GSTO2, CYP2R1, SOST, MAP3K15, CYCSP25, FOPNL, NDUFS7, LYPLAL1, BOLA3, TAS2R13, IL31RA, CD164L2, TRIM69, TRPM6, ARMS2, SRXN1, CACUL1, ENHO, KLK12, KCNIP3, RHOD, MYLIP, XPO5, TICAM1, CNTNAP2, EPHA6, SDK1, ADGRE4P, MARCHF8, LOC107987479, ZNF260, RXFP4, ATOH7, DLEU7, HYLS1, TSPAN33, NUPR1, ITGB1BP2, CPP, FOLH1B, SLC36A1, PABPC1, DNM3, GLCE, DROSHA, SLC29A4, NPW, LDOC1, PGP, IFNL2, IS1, BRD1, COL6A5, SLC24A2, KLK9, QPCT, GCA, CASC2, EBF3, FNDC5, VAMAS6, ADGRA2, SH2B1, CMYA5, FLCN, DCP1B, RLS1, LCE1C, RABGEF1, PCSK1N, AMOT, CBSL, SLC2A12, MCAT, CNTN4, SLCO4C1, RMDN2, FAM78B, REM1, IL23R, MOB3C, FLVCR1, RGCC, SLC35F3, PACERR, PAQR7, XIRP1, GPR162, CRPP1, NLRP6, GOLGA6A, MCIDAS, SNX5, HCAR1, CAVIN4, ADAMTS18, DDX53, CERNA3, TCEANC, LINC02210-CRHR1, PDCD4, SLC30A8, LCE1A, BMPER, RMDN1, CNTN5, C1QTNF6, PLXNA3, MTMR9, LGR4, WNK3, SAGE1, MIR30A, ACD, SLC30A10, POU5F1P4, SLC26A6, MIR31, MIR96, RNPC3, MIR33A, P2RY12, SYBU, POU5F1P3, MFSD1, PDIA2, MIR34B, GORASP1, STYK1, MIR585, MIR593, VKORC1, TTC21B, GSTCD, MSTO1, MCPH1, MIR296, PNPO, RMDN3, MIR637, ADIPOR2, SAP130, RCBTB1, MIR621, BHLHE41, PPP6R3, SLC29A3, MIR608, DRAM1, CARD14, TMEM38A, SLC48A1, MIR509-1, OXR1, HAMP, ZNF77, SLC2A9, MIR202, NGB, GRHL3, PLF, CISD2, SPHK2, MEPE, FAM20C, MIR506, MIR410, MIR425, MIR429, IBD7, PCBP4, MIR451A, BEND3, MIR431, VARS2, KCNQ5, IL21, MIR495, SLC5A7, MIR503, ARHGEF28, MIR499A, MIR98, MIR17HG, XYLT2, XYLT1, VPS11, TRIM67, PAG1, SLC28A3, SRR, GAS5, ANGPTL8, MIR328, PDGFC, BTNL2, SULT1A4, TRPV5, TREML2, MAP9, ANGPTL4, CCNQ, PPP1R14A, IL23A, MUC16, MIR132, MIR140, GHRL, PPR1, ASIC5, ORAI3, SLCO1C1, TSLP, CA14, TRIM47, GPR88, SOX18, MCU, WNT4, KNSTRN, TERF2IP, UCN2, PRRT2, OSER1, MRAP2, SFMBT1, HSPA14, MIR10A, C1QTNF3, PIPOX, GOLM1, MIR122, KCNK9, LOC102723407, CYGB, TLR8, TMEM54, MEX3C, BIRC6-AS1, GLCCI1, TAOK3, MIR4513, ANGPT4, IL17F, PRKAG2, SSH1, TAF7L, MIR222, CDKAL1, MIR200A, MIR200B, WBP1L, HDHD2, MIR206, EMILIN2, MIR1224, MIR543, MIR210, COL21A1, PTPN5, TUBB1, COASY, PDGFD, MIR212, FHOD3, RUBCNL, PTGES2, SVEP1, SLC52A1, CHCHD5, ERCC6L, HOPX, MIR19B1, SLX1A-SULT1A3, PPP1R9B, LINC01672, MIR185, MIR190A, ROBO4, SPATA6, KIF2B, MIR195, NDFIP2, MIR199A1, MIR199A2, CROT, ROPN1, ZGPAT, ALL2, NT5C1A, ALL1, TRPM4, A2M, SELL, AMACR, HNRNPD, HSPA1B, HSPA1A, AGFG1, HPX, HPV18I2, HPCAL1, HNRNPF, SLC29A2, HSPA2, HNF4A, NR4A1, HMOX2, HMGCR, HLA-C, HLA-A, UBE2K, HSPA1L, HSP90AA1, HDAC1, IGFALS, IL4R, IL2RA, IL2, IL1R1, CCN1, IGFBP3, IGFBP1, IFNA13, HTN1, IFNA2, IFNA1, IFI27, IDH2, IDH1, ID1, HTR1E, HDAC2, HBG1, CXCR1, FPR2, GATA3, GALNT2, GAD2, XRCC6, GAST, NR5A1, FXN, FPR1, GHR, FOSB, FOLH1, FLT4, FLI1, FOXO3, FOXM1, FOXC1, GC, GIP, HBA2, GSTM5, HBA1, GYS1, GYPE, GYPB, GYPA, GUCY1B1, GUCA2B, GSTA1, GLI2, GRIA1, GPX3, CXCR3, NPBWR1, GPI, GOT2, GLO1, IL5RA, IL10RA, OGN, MMP8, MTHFD1, MT1A, MSR1, MPV17, MPST, MMP12, MMP10, KMT2A, TRNI, MAP3K10, CXCL9, MET, MEST, MAP3K5, MEFV, ADAM11, MTR, MVD, MBP, NFATC3, NPY2R, NPHS1, NPC1, NPAS2, NOVA2, NHS, NFKB1, NEDD9, MX1, NDUFS4, NDUFA10, PPP1R12A, MYOC, MYL3, MYL2, MYH6, MC3R, MAT1A, IL10RB, PDX1, ITGB3, ITGAX, ITGAM, ITGA2, ISG20, IRF1, IRAK1, INHA, ITPR1, IMPA1, ILK, ILF3, IL15, IL13, IL12B, IL11, ITGB8, ITPR3, MAOA, LCN1, SMAD9, SMAD7, LSS, LRP5, LLGL2, LHCGR, LGALS1, KRT16, JUNB, KRT5, KIT, KIR3DL1, KIR2DS5, KCNN3, KCNH1, JUND, FHL2, FHL1, FGFR4, BMP7, C4BPA, C3AR1, BUB1B, KLF5, BRAF, BNIP1, BMPR1A, BGN, C5, BCL6, BCL2L1, BAAT, ATP7A, ATP6V0A1, ATP5F1B, ATP4A, CAPN5, CA2, ATP12A, CAV3, CDSN, CDR1, CDKN2B, CDH2, SCARB2, CD86, RUNX1T1, CASQ2, CACNA1A, CASP1, CAMK2A, CAMK4, CALD1, CALCR, CALB2, SLC25A20, ATP2B4, ATIC, FGFR1, ACVR2A, AMBP, ALOX15B, ALOX5AP, AHSG, NR0B1, AGXT, ADCYAP1R1, ACP3, AMY1B, ACO1, ACLS, ACHE, ASIC2, ACADSB, ABCA4, ABCA3, AMY1A, AMY1C, ART1, AQP5, ARSL, ARSB, ARRB1, PHOX2A, ARHGAP6, ARHGAP1, ARF6, FASLG, AOC2, APOH, APOC1, APOA4, BIRC3, APEH, APCS, APBB1, AKR1C4, CHGB, CHRM2, DSC3, EIF4E, EFNB2, EFNB1, LPAR1, E2F1, DUSP2, RCAN1, DPAGT1, ENO3, DNTT, DNMT3A, SARDH, DLG4, DIO1, DES, DBI, EMD, EPHA3, CHRM3, F8, FGF10, FDXR, FCGR2B, FBLN2, FANCD2, FABP4, F10, F2RL1, EPHA4, EYA3, ETV5, ESRRG, ERCC3, ERBB2, EPOR, EPHX1, DAG1, DAB2, CYP27B1, CCR7, COL9A1, COL8A1, COL4A2, COL1A2, CNP, CNN2, ABCC2, CCR3, CYP24A1, CLCN7, CLCN3, CLC, CISH, CIRBP, CHRNA4, CHRNA3, COL9A2, COL9A3, COMP, KLF6, CYP7A1, CYP4B1, CYP3A7, CYP2A6, CTSK, CTSG, CTRL, CTF1, CTBP1, CSF3, CRYZ, CREBBP, CLDN7, COX4I1, SLC31A1, ODC1, OPRD1, PSD4, CRLF1, SLC22A8, SLC22A6, TRIP10, NREP, KLF4, ASIC3, GPR37L1, MSC, TGFBRAP1, MTA2, XPR1, SLC28A2, HGS, P2RX6, RGN, USP2, COX5A, NTN1, PKD2L1, ARHGEF10, FIG4, RB1CC1, TOX, SLK, PPP6R2, GREB1, PHF14, ABCG1, NCR1, CARTPT, NPEPPS, ADAMTS1, ADAMTS4, HOMER1, GSTO1, MED23, ANGPTL1, NAT8, RABGAP1L, TAM, RGS20, TNFSF11, FCN3, AGPS, SEMA7A, FOXN1, AXIN2, LAP, TP63, PRRC2A, ST8SIA4, SCG2, IL1R2, NPHS2, YY1, XRCC1, PSMG1, AKR1C3, SOCS3, CCN4, F2RL3, KALRN, TRPA1, MGAM, WASF1, PER2, ALKBH1, TMEM11, IRS2, NRP1, HESX1, IL18RAP, TNFRSF10B, TNFSF14, RNGTT, MBTPS1, WASHC5, PUM3, OPRK1, MLXIP, KDM1A, FAIM2, PDCD11, SCAP, SIRT2, SACM1L, CARD8, ZNF652, TBC1D9, PTGDR2, POLI, CHEK2, RASSF1, SLC2A6, WDHD1, CORO1A, NCDN, ZCCHC14, PDIA5, TRS-AGA2-3, ATP6V0A2, RBFOX2, MMD, TRAM1, NPTXR, HEY1, SF3B3, MLYCD, LPIN1, SIRT5, WWC1, ADGRL3, CLEC16A, TASOR, NBEAL2, RRS1, YWHAQ, BTG3, RBM8A, CEBPZ, RAMP3, ABCC4, MSLN, GDF11, ANGPTL7, CALCRL, TSHZ1, BCAP31, BET1, PTPRU, NR1H3, HDAC5, SRA1, SLC12A6, FGFBP1, MVP, STUB1, APBB3, GPR75, DCTN6, FGL2, HPSE, WASF3, GJB6, AHCYL1, KDM5B, TNFSF13B, TXNIP, AKR1A1, HEXIM1, P3H4, ZNRD2, APPBP2, STK25, TFG, TLR6, XPC, NSD2, LAT2, PROS1, PTGDR, TAS2R38, PTBP1, PYY, PSMB8, PSG5, PSEN2, PRNP, PTPRO, PRKCG, PRH2, PRH1, SRGN, PRF1, PPP6C, PPP1CB, PTPRD, PXN, PPIB, RLN1, RRAS, RRAD, RPS6, RPL13, BRD2, RMRP, RLN2, RIEG2, RAC2, RHO, RGS1, REG1A, RBM4, RASA1, RAP1B, RAP1A, PPL, CTSA, VTN, PAM, PDE2A, PCYT1A, PCOS1, PCNA, PC, PAX5, CNTN3, PAK3, PDR, PAK1, P4HB, P2RY2, P2RX4, P2RX1, OTC, OPRM1, PDPK1, PEE1, POU5F1, PLAU, PON2, PODXL, EXOSC10, PLOD1, PLD2, PLCG1, PLCB3, PLAG1, PFKFB3, PLA2G5, PLA2G4A, PLA2G1B, PKM, PIN1, SERPINA1, PHB, S100A1, SORT1, SAA1, TBXA2R, TERT, TEK, TDO2, TCOF1, TCN2, TCF7L2, TBX3, TBX5, TG, TAP1, TAGLN, SYT1, SULT1A3, STAT5A, STAT1, TRIM21, TFRC, THRA, SAA2, UBTF, VIPR2, VDAC3, VDAC2, VDAC1, VAV2, VASP, UGCG, TTN, TIMP2, PHLDA2, TRV-AAC1-4, TRIO, HSP90B2P, TPH1, TPD52, TNFAIP3, SRY, SREBF1, SPRR2A, SDHC, SLC5A1, SLC4A1, SLC3A2, ST3GAL4, SI, SGCA, SEMA3F, SDC1, SPARC, CXCL5, CCL22, CCL13, CCL11, CCL7, SCN8A, SCD, SMTN, SLC6A9, SLC16A1, SLC19A1, SP1, SOS1, SORL1, SORD, SNX1, FSCN1, SNAP25, SMS, SMO, SMN2, SMN1, HLTF, SLC22A5, SLC22A4, SLC22A3, H3P23
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Crouzonodermoskeletal Syndrome
Wikipedia
These cases occur in people with no history of the disorder in their family. [ citation needed ] Diagnosis [ edit ] This section is empty. You can help by adding to it . ( October 2017 ) Treatment [ edit ] This section is empty. You can help by adding to it . ( October 2017 ) References [ edit ] ^ Herman, TE; Sargar, K; Siegel, MJ (Feb 2014). ... "Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3". Am J Med Genet . 98 (1): 75–91. doi : 10.1002/1096-8628(20010101)98:1<75::AID-AJMG1010>3.0.CO;2-6 . ... "Let's call it "Crouzonodermoskeletal syndrome" so we won't be prisoners of our own conventional terminology". Am J Med Genet . 84 (1): 74. doi : 10.1002/(SICI)1096-8628(19990507)84:1<74::AID-AJMG14>3.0.CO;2-R .
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Arachnoid Cyst
Wikipedia
CS1 maint: multiple names: authors list ( link ) ^ a b Cameron AD. "Psychotic phenomena with migraine and an arachnoid cyst", Progress in Neurology and Psychiatry 2002 Mar-Apr 6(2) http://www.escriber.com/Progress/Features.asp? ... Wien. Klin. Wochenschr . 118 Suppl 2: 85–8. doi : 10.1007/s00508-006-0540-2 . ... "Suprasellar arachnoid cysts: endoscopy versus microsurgical cyst excision and shunting". Br J Neurosurg . 21 (3): 276–80. doi : 10.1080/02688690701339197 . ... "Endoscopic management of intracranial cysts" . Neurosurg Focus . 19 (6): E7. doi : 10.3171/foc.2005.19.6.8 . PMID 16398484 . ^ Van Beijnum J, Hanlo PW, Han KS, Ludo Van der Pol W, Verdaasdonk RM, Van Nieuwenhuizen O (May 2006). ... "Arachnoid cysts: case series and review of the literature" . Neurosurg Focus . 22 (2): E7. doi : 10.3171/foc.2007.22.2.7 . PMID 17608350 . ^ Weber F, Knopf H (January 2006).
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Pseudomonas Infection
Wikipedia
"Septicaemia in patients with AIDS". Trans. R. Soc. Trop. Med. Hyg . 84 Suppl 1: 14–6. doi : 10.1016/0035-9203(90)90449-o . ... The American Journal of Medicine . 91 (3): S72–S75. doi : 10.1016/0002-9343(91)90346-Y . hdl : 2027.42/29131 . ... PMID 10826790 . ^ López-Romalde S, Magariños B, Ravelo C, Toranzo AE, Romalde JL (2003). "Existence of two O-serotypes in the fish pathogen Pseudomonas anguilliseptica". Vet. Microbiol . 94 (4): 325–33. doi : 10.1016/S0378-1135(03)00124-X . ... Med . 76 (1): 62–8. doi : 10.1016/0002-9343(84)90751-4 . PMID 6419604 . External links [ edit ] Classification D ICD - 10 : B96.5, J15.1, P23.5 ICD - 9-CM : 041.7 , 482.1 MeSH : D011552 v t e Proteobacteria -associated Gram-negative bacterial infections α Rickettsiales Rickettsiaceae / ( Rickettsioses ) Typhus Rickettsia typhi Murine typhus Rickettsia prowazekii Epidemic typhus , Brill–Zinsser disease , Flying squirrel typhus Spotted fever Tick-borne Rickettsia rickettsii Rocky Mountain spotted fever Rickettsia conorii Boutonneuse fever Rickettsia japonica Japanese spotted fever Rickettsia sibirica North Asian tick typhus Rickettsia australis Queensland tick typhus Rickettsia honei Flinders Island spotted fever Rickettsia africae African tick bite fever Rickettsia parkeri American tick bite fever Rickettsia aeschlimannii Rickettsia aeschlimannii infection Mite-borne Rickettsia akari Rickettsialpox Orientia tsutsugamushi Scrub typhus Flea-borne Rickettsia felis Flea-borne spotted fever Anaplasmataceae Ehrlichiosis : Anaplasma phagocytophilum Human granulocytic anaplasmosis , Anaplasmosis Ehrlichia chaffeensis Human monocytotropic ehrlichiosis Ehrlichia ewingii Ehrlichiosis ewingii infection Rhizobiales Brucellaceae Brucella abortus Brucellosis Bartonellaceae Bartonellosis : Bartonella henselae Cat-scratch disease Bartonella quintana Trench fever Either B. henselae or B. quintana Bacillary angiomatosis Bartonella bacilliformis Carrion's disease , Verruga peruana β Neisseriales M+ Neisseria meningitidis/meningococcus Meningococcal disease , Waterhouse–Friderichsen syndrome , Meningococcal septicaemia M− Neisseria gonorrhoeae/gonococcus Gonorrhea ungrouped: Eikenella corrodens / Kingella kingae HACEK Chromobacterium violaceum Chromobacteriosis infection Burkholderiales Burkholderia pseudomallei Melioidosis Burkholderia mallei Glanders Burkholderia cepacia complex Bordetella pertussis / Bordetella parapertussis Pertussis γ Enterobacteriales ( OX− ) Lac+ Klebsiella pneumoniae Rhinoscleroma , Pneumonia Klebsiella granulomatis Granuloma inguinale Klebsiella oxytoca Escherichia coli : Enterotoxigenic Enteroinvasive Enterohemorrhagic O157:H7 O104:H4 Hemolytic-uremic syndrome Enterobacter aerogenes / Enterobacter cloacae Slow/weak Serratia marcescens Serratia infection Citrobacter koseri / Citrobacter freundii Lac− H2S+ Salmonella enterica Typhoid fever , Paratyphoid fever , Salmonellosis H2S− Shigella dysenteriae / sonnei / flexneri / boydii Shigellosis , Bacillary dysentery Proteus mirabilis / Proteus vulgaris Yersinia pestis Plague / Bubonic plague Yersinia enterocolitica Yersiniosis Yersinia pseudotuberculosis Far East scarlet-like fever Pasteurellales Haemophilus : H. influenzae Haemophilus meningitis Brazilian purpuric fever H. ducreyi Chancroid H. parainfluenzae HACEK Pasteurella multocida Pasteurellosis Actinobacillus Actinobacillosis Aggregatibacter actinomycetemcomitans HACEK Legionellales Legionella pneumophila / Legionella longbeachae Legionnaires' disease Coxiella burnetii Q fever Thiotrichales Francisella tularensis Tularemia Vibrionaceae Vibrio cholerae Cholera Vibrio vulnificus Vibrio parahaemolyticus Vibrio alginolyticus Plesiomonas shigelloides Pseudomonadales Pseudomonas aeruginosa Pseudomonas infection Moraxella catarrhalis Acinetobacter baumannii Xanthomonadaceae Stenotrophomonas maltophilia Cardiobacteriaceae Cardiobacterium hominis HACEK Aeromonadales Aeromonas hydrophila / Aeromonas veronii Aeromonas infection ε Campylobacterales Campylobacter jejuni Campylobacteriosis , Guillain–Barré syndrome Helicobacter pylori Peptic ulcer , MALT lymphoma , Gastric cancer Helicobacter cinaedi Helicobacter cellulitis
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Dysphrenia
Wikipedia
References [ edit ] Chouinard G, Jones BD. Neuroleptic-induced supersensitivity psychosis: clinical and pharmacologic characteristics.
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Oncovirus
Wikipedia
Please help improve this section by adding citations to reliable sources . ... PMID 16963733 . ^ Wiest T, Schwarz E, Enders C, Flechtenmacher C, Bosch FX (February 2002). "Involvement of intact HPV16 E6/E7 gene expression in head and neck cancers with unaltered p53 status and perturbed pRb cell cycle control" . ... Cold Spring Harb. Symp. Quant. Biol . 44 (1): 569–84. doi : 10.1101/sqb.1980.044.01.059 . ... New Science Press. ISBN 978-1-904455-99-8 . ^ a b c Levine AJ (February 2009). ... PMID 19150725 . ^ Scheffner M, Huibregtse JM, Vierstra RD, Howley PM (November 1993). "The HPV-16 E6 and E6-AP complex functions as a ubiquitin-protein ligase in the ubiquitination of p53".
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Beare–stevenson Cutis Gyrata Syndrome
Wikipedia
Diagnosis [ edit ] This section is empty. You can help by adding to it . ( April 2017 ) Treatment [ edit ] This section is empty. You can help by adding to it . ( April 2017 ) Incidence [ edit ] Beare–Stevenson cutis gyrata syndrome is so rare that a reliable incidence cannot be established as of yet; fewer than 25 patients with the condition have been reported. ... Retrieved 14 March 2019 . ^ http://ghr.nlm.nih.gov/condition/beare-stevenson-cutis-gyrata-syndrome The Genetic Home Reference entry on Beare-Stevenson cutis gyrata syndrome ^ a b Hall BD, Cadle RG, Golabi M, Morris CA, Cohen MM (September 1992).
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Channelopathy
Wikipedia
. ^ Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS, Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht JL, Salonen O, Barkovich AJ, Poduri A, Wilke M, de Wit MC, Mancini GM, Sztriha L, Im K, Amrom D, Andermann E, Paetau R, Lehesjoki AE, Walsh CA, Lehtinen MK (September 2018). "V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development" . Neuron . 99 (5): 905–913.e7. doi : 10.1016/j.neuron.2018.07.052 . ... The Channelopathy Foundation - Foundation for Ion Channel diseases Cystic Fibrosis Foundation Rare Diseases Clinical Research Network v t e Diseases of muscle , neuromuscular junction , and neuromuscular disease Neuromuscular- junction disease autoimmune Myasthenia gravis Lambert–Eaton myasthenic syndrome Neuromyotonia Myopathy Muscular dystrophy ( DAPC ) AD Limb-girdle muscular dystrophy 1 Oculopharyngeal Facioscapulohumeral Myotonic Distal (most) AR Calpainopathy Limb-girdle muscular dystrophy 2 Congenital Fukuyama Ullrich Walker–Warburg XR dystrophin Becker's Duchenne Emery–Dreifuss Other structural collagen disease Bethlem myopathy PTP disease X-linked MTM adaptor protein disease BIN1-linked centronuclear myopathy cytoskeleton disease Nemaline myopathy Zaspopathy Channelopathy Myotonia Myotonia congenita Thomsen disease Neuromyotonia / Isaacs syndrome Paramyotonia congenita Periodic paralysis Hypokalemic Thyrotoxic Hyperkalemic Other Central core disease Mitochondrial myopathy MELAS MERRF KSS PEO General Inflammatory myopathy Congenital myopathy v t e Diseases of ion channels Calcium channel Voltage-gated CACNA1A Familial hemiplegic migraine 1 Episodic ataxia 2 Spinocerebellar ataxia type-6 CACNA1C Timothy syndrome Brugada syndrome 3 Long QT syndrome 8 CACNA1F Ocular albinism 2 CSNB2A CACNA1S Hypokalemic periodic paralysis 1 Thyrotoxic periodic paralysis 1 CACNB2 Brugada syndrome 4 Ligand gated RYR1 Malignant hyperthermia Central core disease RYR2 CPVT1 ARVD2 Sodium channel Voltage-gated SCN1A Familial hemiplegic migraine 3 GEFS+ 2 Febrile seizure 3A SCN1B Brugada syndrome 6 GEFS+ 1 SCN4A Hypokalemic periodic paralysis 2 Hyperkalemic periodic paralysis Paramyotonia congenita Potassium-aggravated myotonia SCN4B Long QT syndrome 10 SCN5A Brugada syndrome 1 Long QT syndrome 3 SCN9A Erythromelalgia Febrile seizure 3B Paroxysmal extreme pain disorder Congenital insensitivity to pain Constitutively active SCNN1B / SCNN1G Liddle's syndrome SCNN1A / SCNN1B / SCNN1G Pseudohypoaldosteronism 1AR Potassium channel Voltage-gated KCNA1 Episodic ataxia 1 KCNA5 Familial atrial fibrillation 7 KCNC3 Spinocerebellar ataxia type-13 KCNE1 Jervell and Lange-Nielsen syndrome Long QT syndrome 5 KCNE2 Long QT syndrome 6 KCNE3 Brugada syndrome 5 KCNH2 Short QT syndrome KCNQ1 Jervell and Lange-Nielsen syndrome Romano–Ward syndrome Short QT syndrome Long QT syndrome 1 Familial atrial fibrillation 3 KCNQ2 BFNS1 Inward-rectifier KCNJ1 Bartter syndrome 2 KCNJ2 Andersen–Tawil syndrome Long QT syndrome 7 Short QT syndrome KCNJ11 TNDM3 KCNJ18 Thyrotoxic periodic paralysis 2 Chloride channel CFTR Cystic fibrosis Congenital absence of the vas deferens CLCN1 Thomsen disease Myotonia congenita CLCN5 Dent's disease CLCN7 Osteopetrosis A2, B4 BEST1 Vitelliform macular dystrophy CLCNKB Bartter syndrome 3 TRP channel TRPC6 FSGS2 TRPML1 Mucolipidosis type IV Connexin GJA1 Oculodentodigital dysplasia Hallermann–Streiff syndrome Hypoplastic left heart syndrome GJB1 Charcot–Marie–Tooth disease X1 GJB2 Keratitis–ichthyosis–deafness syndrome Ichthyosis hystrix Bart–Pumphrey syndrome Vohwinkel syndrome ) GJB3 / GJB4 Erythrokeratodermia variabilis Progressive symmetric erythrokeratodermia GJB6 Clouston's hidrotic ectodermal dysplasia Porin AQP2 Nephrogenic diabetes insipidus 2 See also: ion channelsSCN4A, SCN5A, KCNQ1, CACNA1A, SCN9A, TRPV4, SCN1A, RYR2, KCNK3, AQP4, GCK, TYRP1, STIM1, TBPL1, IDS, ABCC9, KCNJ6, GLUD1, KCNJ10, KCNE2, HADH, KCNA5, ABCC8, KCNJ18, TRPM4, CLIC2, CLCN1, CFTR, SHANK3, NALCN, PKP2, KCNH2, SPG7, SLC16A1, SLC2A1, SCN10A, FST, MHS3, KCNE3, MALAT1, HCN1, UNC80, ASB10, HVCN1, UNC79, LGALS14, ANO1, CNGB3, SEC61A1, MCTS1, MCAT, PANX1, SCN11A, AKAP9, SCN3A, ANK2, SCD, CLCA1, GJB1, CBLIF, EGR1, CNGA3, CMA1, CLCN5, CLCN2, CAV1, ATXN1, CACNA2D1, CACNA1S, CACNA1F, CACNA1D, CACNA1C, ATP1A3, ATP1A2, HSD17B10, UBE2K, HLA-DRB5, HSPB2, PMM2, PDC, P2RX7, ATP6, MECP2, KCNMA1, KCNK2, KCNJ11, KCNJ5, KCNJ3, KCNJ2, KCNE1, KCNA4, KCNA2, INSR, TRPM1
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Trichophagia
Wikipedia
"Fatal case of Rapunzel syndrome in neglected child". Forensic Sci. Int . 190 (1–3): e5–7. doi : 10.1016/j.forsciint.2009.05.008 . ... "Clinical characteristics of trichotillomania with trichophagia" . Compr Psychiatry . 49 (6): 579–84. doi : 10.1016/j.comppsych.2008.05.002 .
- Langerhans Cell Sarcoma Wikipedia