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Enteroinvasive Escherichia Coli
Wikipedia
Enteroinvasive Escherichia coli Specialty Infectious disease Enteroinvasive Escherichia coli ( EIEC ) is a type of pathogenic bacteria whose infection causes a syndrome that is identical to shigellosis , with profuse diarrhea and high fever. ... Enterohemorrhagic E. coli (EHEC): A type of EHEC, E. coli O157:H7, can cause bloody diarrhea and hemolytic uremic syndrome (anemia and kidney failure). Enterotoxigenic E. coli (ETEC) produces a toxin that acts on the intestinal lining, and is the most common cause of traveler's diarrhea . ... Retrieved June 8, 2015 . ^ Escherichia coli , enteroinvasive Material Data Safety Sheets External links [ edit ] Classification D ICD - 10 : A04.2 ICD - 9-CM : 008.03 v t e Escherichia coli Outbreaks 1993 Jack in the Box 1996 Odwalla 2000 Walkerton 2005 South Wales (O157) 2006 North American (spinach; O157:H7) 2006 North American (multiple; O157:H7) 2009 United Kingdom 2011 Germany (O104:H4) 2015 United States Genes CPS operon DnaG Fis FNR regulon OmpT RecBCD RpoE RpoF RpoN RpoS Strains Enterohemorrhagic Enteroinvasive Enterotoxigenic O104:H21 O104:H4 O121 O157:H7 Verotoxin-producing Related Aerobactin Coliform index Long-term evolution experiment EcoCyc Enteroaggregative Molecular biology Hok/sok system LacUV5 Min System Pathogenic EnvZ/OmpR Rho factor T4 rII system Theodor Escherich 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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Mental Retardation, X-Linked, Syndromic, Houge Type
Omim
A number sign (#) is used with this entry because of evidence that Houge-type X-linked syndromic mental retardation (MRXSHG) is caused by hemizygous or heterozygous mutation in the CNKSR2 gene (300724) on chromosome Xp22. Description The Houge type of X-linked syndromic mental retardation is characterized by delayed development, intellectual disability, speech and language delay, and early-onset seizures.
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Pityriasis Lichenoides Et Varioliformis Acuta
Wikipedia
External links [ edit ] DermNet scaly/pityriasis-lichenoides Classification D ICD - 10 : L41.0 ICD - 9-CM : 696.2 External resources eMedicine : derm/334 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 Papulosquamous disorders Psoriasis Pustular Generalized pustular psoriasis ( Impetigo herpetiformis ) Acropustulosis / Pustulosis palmaris et plantaris ( Pustular bacterid ) Annular pustular psoriasis Localized pustular psoriasis Other Guttate psoriasis Psoriatic arthritis Psoriatic erythroderma Drug-induced psoriasis Inverse psoriasis Napkin psoriasis Seborrheic-like psoriasis Parapsoriasis Pityriasis lichenoides ( Pityriasis lichenoides et varioliformis acuta , Pityriasis lichenoides chronica ) Lymphomatoid papulosis Small plaque parapsoriasis ( Digitate dermatosis , Xanthoerythrodermia perstans ) Large plaque parapsoriasis ( Retiform parapsoriasis ) Other pityriasis Pityriasis rosea Pityriasis rubra pilaris Pityriasis rotunda Pityriasis amiantacea Other lichenoid Lichen planus configuration Annular Linear morphology Hypertrophic Atrophic Bullous Ulcerative Actinic Pigmented site Mucosal Nails Peno-ginival Vulvovaginal overlap synromes with lichen sclerosus with lupus erythematosis other: Hepatitis-associated lichen planus Lichen planus pemphigoides Other Lichen nitidus Lichen striatus Lichen ruber moniliformis Gianotti–Crosti syndrome Erythema dyschromicum perstans Idiopathic eruptive macular pigmentation Keratosis lichenoides chronica Kraurosis vulvae Lichen sclerosus Lichenoid dermatitis Lichenoid reaction of graft-versus-host disease
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Alzheimer Disease
Medlineplus
Some evidence indicates that people with Down syndrome have an increased risk of developing Alzheimer disease. Down syndrome, a condition characterized by intellectual disability and other health problems, occurs when a person is born with an extra copy of chromosome 21 in each cell. As a result, people with Down syndrome have three copies of many genes in each cell, including the APP gene, instead of the usual two copies. Although the connection between Down syndrome and Alzheimer disease is unclear, the production of excess amyloid beta peptide in cells may account for the increased risk. People with Down syndrome account for less than 1 percent of all cases of Alzheimer disease.APP, ACE, TREM2, ADAM10, APOE, PSEN1, GSK3B, HFE, MAPT, PLAU, NPY, BCL2, CASP3, BDNF, IDE, INSR, IL1B, LEP, BACE1, IGF2, IGF1R, ATP5F1A, INS, BAX, CR1, A2M, ABCA7, TOMM40, CD2AP, BIN1, EPHA1, CLU, PICALM, NOS3, PSEN2, APOC1, MPO, SORL1, VSNL1, INPP5D, NECTIN2, MS4A4A, PCDH11X, CASS4, BCHE, MIR146A, CYP46A1, DHCR24, CHRNA7, NCSTN, VEGFA, DPYSL2, PRNP, ESR1, PPARG, RELN, HMOX1, ACHE, CST3, MAOB, TNF, MTHFR, IGF1, CD33, TFAM, IL6, CYP2D6, CRH, SOD2, UNC5C, PLCG2, TF, ABI3, WWOX, SLC30A6, CHRNB2, ARC, PGRMC1, F2, CALM1, EIF2S1, HLA-DRB5, ENO1, TPI1, IGF2R, SLC30A4, MIR296, SLC2A4, MIR100, IQCK, MIR375, AMFR, SNAR-I, ADAMTS1, MAPK14, PIN1, PYY, PTGS2, S100B, PPARGC1A, NOS2, NGFR, NGF, NFE2L2, SOD1, SYP, CDK5, NGB, MIR505, GAPDHS, MME, MAP2, CTNNB1, TPP1, LRP1, IRS1, CHAT, GAPDH, MIR4467, MIR3622B, AGER, MIR766, MIR708, CAV1, NTRK2, PTGS1, APLP2, ADAM17, MFN2, DNM1, HSF1, GSR, IL33, CCR5, HSPD1, HSPB1, CIB1, CASP8, IKBKB, SERPINF1, ATP7A, MT2A, ADAM9, INS-IGF2, BCL2L2, CASP9, GAB2, PTK2B, PLCB1, ABCA1, GRN, CASP12, SQSTM1, FERMT2, HLA-DRB1, NFIC, CSF1R, APOB, MARK4, HSPG2, MS4A6A, CELF1, VCP, SYNJ1, ZCWPW1, MS4A4E, APH1B, APOC2, F13A1, EXOC3L2, PLXNA4, ADAMTS4, AKAP9, MADD, DST, PILRA, FRMD4A, LAMP1, SLC24A4, GLIS3, SPON1, CADPS2, IL34, COL18A1, TRIP4, SPI1, TGFB2, BCL3, MTHFD1L, AICDA, IL6R, DCHS2, MEGF10, SLC16A7, EPHX2, NDUFAF6, DSG2, OSBPL6, CELF2, UBE2L3, SPPL2A, MAPK7, CDH13, LAMA1, SGK1, SUCLG2, LUZP2, PTPRG, ST6GAL1, AP2A2, RBFOX1, SORCS3, TSPOAP1-AS1, TLN2, ZAP70, ALDH1A2, TCF7L2, FMN2, OTOF, EXOC4, HSD17B10, DNM1L, ALOX5, GULOP, HTR2A, AHCYL1, SDR42E2, HTR6, GTF2H1, GRM5, IAPP, AHSA1, STAG3, ALB, FARP1, TSHZ1, HRES1, AGFG2, DCAF7, SIGMAR1, BCKDK, RTN3, TPPP, HSPA4, HCLS1, HSP90AA1, G3BP1, PGAM5P1, BACE1-AS, KHDRBS1, ALDH2, CFH, HCRT, GPC6, ABCA8, GLP1R, NR3C1, TNRC6A, IL19, PARVB, DDX25, BZW2, FCN2, FGF10, GOLIM4, LINC00476, HPGDS, FANCD2, PDE7B, SIGLEC7, TSPAN16, TRPC4AP, POLDIP2, CNTNAP2, RNF19A, BACE2, UBQLN1, ITSN2, GRIN2B, ZGLP1, BCAS3, EPDR1, TMED9, ENO2, CYCS, ANXA1, EPHB2, EPO, RAPGEF6, APH1A, LARS1, EYA4, SNX9, ESR2, WAC, SLC8A1-AS1, DCTN4, RMDN1, QPCT, MTOR, SGK3, FBXL7, SZT2, GIP, ACSL6, WWC1, CLEC16A, KAZN, LINC01672, PRRC2C, COLGALT2, PLD3, HECW1, ZNF292, MYO16, DKK1, SIRT2, ACOT7, PSIP1, CLASRP, LINC00271, SIRT3, SIRT1, GFAP, NUP62, FYN, CBLC, INHCAP, TRIM51CP, GABPA, GABRA2, GABRG3, DAPK2, SMUG1, GAP43, GATA1, GCG, GCHFR, TARDBP, NCS1, GDNF, HDAC6, RAB3D, MVP, OGG1, LINC02268, LINC02325, SOAT1, ACTG2, ACTG1, SNCG, SNCA, SNCB, SNAP25, NOS1, ACTB, MEF2C-AS1, SLC6A4, NPC1, SLC6A3, GEMIN7-AS1, SLC1A2, LINC01508, LINC01725, NEFL, COX2, TNFRSF1B, STAG3L5P, TLR4, TLR2, MSH2, THY1, MT3, TH, SST, STAG3L5P-PVRIG2P-PILRB, TGFB1, TFF1, RNR2, LINC02653, LINC01712, TCF3, NRGN, CX3CL1, ELMO1, CCL2, PIK3CG, ABCA2, PLA2G1B, EIF2AK2, SERPINA3, PLG, MAPK8, MAPK1, PRKCB, PRKCA, PRKAB1, PRKAA2, PRKAA1, PMS2P1, POLD1, PTPA, PON1, PIK3CD, PIK3CB, PIK3CA, MOK, UPK3B, SORT1, ROS1, SERPINE1, REST, REN, RELB, RAC1, LINC01965, PVR, PVALB, PTPRA, LINC00972, ABCB1, LINC02008, MTCO2P12, TP53, OVCH1-AS1, MOBP, MNAT1, SLC4A8, AGT, INSIG1, AZIN1-AS1, EIF3E, FHL5, IRF2, GSTO1, ITM2B, GRAP2, LIPG, ADIPOQ, KL, MSC, LRAT, AP4M1, CCRL2, IL18, IL17A, IL12A, ST18, IFNG, ARL17B, AKT1, AIF1, KRBOX1, IGFALS, HDAC9, PHF14, IL10, IL1A, ALOX12-AS1, MICAL2, IL2RB, IL4, CLOCK, CXCL8, KCNN2, MPZL1, HERC2, VDR, TFEB, MAOA, COX10-AS1, ZNF232, YWHAZ, VLDLR, PARP1, UTRN, BCAM, UCHL1, UBB, TYROBP, AFF1, TTR, TRPM1, MMP9, AIMP2, LTBP2, KNG1, CRADD, CACNA1G, LAMC2, RPSA, CDK5R1, SUCLA2, LCN2, LDLR, BECN1, LPL, PDE5A, ABCB11, APOC4-APOC2, KHSRP, DENR, AGPS, LPA, CDKAL1, PPARA, MEIKIN, COL4A4, CRK, CEACAM22P, SCIMP, CREB1, CR1L, ZNF862, SH2D4B, CP, PNPLA7, SIMC1, GGACT, COMT, COL12A1, FAM181A, BRCA2, PPP1R37, GPR141, TENM3-AS1, CNR2, L3MBTL4, UBXN11, ACKR2, TMEM132C, CASTOR3, CLPTM1, STRADA, FNIP1, CDCA5, NLRP3, APOA1, CRMP1, KAT8, CSMD1, CLMN, PINK1, CYP8B1, AHNAK, MIR132, MIR107, CUX1, POTEM, PPP1R3B, FAS, SAP30L, ANKRD55, CTSD, CTSB, GEMIN7, EHMT1, LINC01184, CTNNA2, LINC01185, TMC5, THSD4, CCDC134, SP6, LINC01567, PDCD1LG2, SETD7, APOD, BHMG1, CSF2, HYI, BLOC1S3, TSPO, CHRNA4, CHRNA2, TAS2R62P, C3orf67, C9orf72, CCDC83, CCDC89, KDM1B, CD14, TGM6, ATXN7L1, RSPO4, ADGRF2, STH, TAS2R64P, CALHM1, RUNX1T1, PPP1R42, ALPK2, PCSK9, CAT, ANKRD31, CASP6, NKAIN3, TRIQK, CALB1, STEAP1B, CASP1, EPHA1-AS1, CAPN1, APOC4, FAM181A-AS1, NKPD1, SPRED2, CD36, SCARB1, PLPP4, MED12L, ARAP2, CHN2, CHI3L1, ACTBL2, C10orf71, MCIDAS, LRRK2, AKR1C4, ANO4, AGBL1, CEACAM20, ZNF813, RMDN3, CETP, CDR1, LINC00343, TCAM1P, APOC1P1, IGSF23, RMDN2, CDK1, SLC25A48, NKAIN2, FSIP1, CD68, BMPER, C3, CD40, CYP19A1, CRP, NIT2, ANO3, DLG4, ARHGAP20, RCAN1, WDR41, NDUFA12, STK32B, EDEM2, DSCAML1, RNF165, SH3RF1, DYRK1A, MIR29A, SYBU, AQP4, APBB1, DLX5, DBN1, PALM2AKAP2, CEACAM19, DPP4, IL6-AS1, ARVCF, CDC42SE2, DMXL1, TULP4, DAPK1, PMS2CL, POTEKP, MIR34A, VAT1L, OLR1, HDAC2, LRP8, GSN, CCL11, S100A9, COL25A1, POTEF, KLK6, BLMH, HSD17B7, P2RX7, COX8A, ABCB6, PRRT2, IL2, SORCS1, NR1I2, MAPK3, ITGAM, CASR, ATP7B, VDAC1, EGR1, PDE4A, RAB5A, SUMO1, NRG1, OXER1, NTRK1, TFCP2, ANK1, CSNK1D, DLST, APLP1, BLVRA, NFIB, IL1RN, HTT, ACAT1, PLA2G4A, NFIX, NLRP1, GPRC6A, HMGCR, PPID, LPAR3, FZD4, REG1A, MRGPRX1, LRP2, DBH, PSENEN, VPS35, ESCO1, HSD11B1, VN1R17P, SOX2, AGTR1, XBP1, MIR155, MRGPRX4, MRGPRX3, GAL, GPR151, IL13, PAEP, OGDH, GPR166P, STAT3, SET, NFIA, PLB1, AR, LGR6, DHRS11, ABCG2, C4A, KCNIP3, HSD17B13, ABCG1, TTBK1, NOTCH1, EIF2AK3, SLCO6A1, CHMP2B, RBM45, CD44, RIPK1, APBA1, GSTK1, ADNP, ICAM1, BRCA1, APCS, TNFRSF1A, NFKB1, CNTF, MMP3, KLC1, LBP, CTNNA3, SGSM3, FGF2, C4B, HIF1A, CREBBP, SERPINA1, TMEM106B, GRIA1, GRIA2, ECE1, C4B_2, GSAP, OGA, TFRC, PLA2G6, ST3GAL4, PAWR, MFAP1, KAT5, GSTM1, APRT, COX1, HP, NTF3, MIR206, FPR2, CDC42, FUS, MARK1, FGF1, PREP, C5AR1, PON2, MIR29C, CALB2, PDIK1L, SYK, S100A1, CH25H, SREBF2, COX5A, GRIN2A, VCAM1, TMED10, GSTP1, KLK8, PHF1, CXCL10, MEFV, SP1, GJA1, IGFBP3, SLC17A7, CYP3A4, FOXO3, HMGA1, SLC11A2, XPR1, MARK2, PPIF, CRHR1, SHANK3, MYC, CD40LG, CPOX, FKBP5, ANPEP, CAST, C1D, FKBP4, HSPA1A, FLT1, MIF, PLA2G2A, CX3CR1, CSF3, IFNB1, KALRN, PLTP, STXBP3, DDR1, PWAR1, PRDX2, TP63, VIM, IL23A, F2RL3, MMP14, MEF2C, TREM1, TMED10P1, NAT2, MIR342, SAMD9, RAB7A, PGR-AS1, TRPM2, EGFR, ADRB2, CLDN5, ETS2, SYT1, TIMP1, NME8, ELANE, F2R, CD59, EPHA4, CBS, MSMB, APLN, MMP2, MYCL, CALML5, SYN1, XRCC1, TGM2, EEF2, PLA2G7, ELAVL2, EDN1, TMEM97, HMGB1, MIR455, HTRA1, BPIFA2, SLC52A2, NQO1, TUBA1B, FOS, CRYAB, SLC2A1, GPR3, LGMN, SLC2A3, RIDA, FN1, ABCA4, HSPA1B, PECAM1, PTEN, HSPA8, HLA-A, PTPN1, HAMP, TXNIP, GRM2, P4HB, LIN28A, PSPH, GSTT1, CCN2, DECR1, CPLX1, BCYRN1, NES, POU5F1P4, MIR21, GRK5, POU5F1, NTSR1, MIR212, PRKN, LINC02210-CRHR1, HSPA5, DLD, DAB1, HTRA2, POU5F1P3, MIR137, DNAH8, MAPK10, GH1, SERPING1, ADAMTS2, EEF2K, GSTO2, ROCK2, NEDD9, SPTBN1, NTN1, CEBPD, GDF2, CEBPB, PWAR4, SYNM, IGFBP2, GLUL, ABCC9, ATM, PSPN, PTPRC, MIR29B1, RANBP9, NDRG2, CNR1, RTN4R, PTBP1, AQP1, PDK1, MIR106B, PDE4D, ARNTL, PRDX1, ADM, RENBP, POMC, PTPN4, MS, PDGFRB, P2RY2, MIR142, PDE9A, SSTR4, KLK3, BCL2A1, C2, SRPK2, NFATC2, ADCYAP1, LRRTM3, PLD1, NUBP1, MIR424, ATF4, BSG, MIR29B2, PPY, BMP4, TBP, SLC18A3, POLB, NOTCH3, SLC18A2, NPTX2, MTR, SI, MIR222, SH3GL2, ND2, NR4A2, SELENOP, CXCL12, CCL5, ATXN1, CALM3, ITGAX, IFNA13, DISC1, OPTN, HTR1F, HTR4, WNT3A, COL11A2, C20orf181, IFNA1, KEAP1, HDAC4, KLK4, SEMA6A, LRRC4, CRTC1, IL9, DAO, ALOX15, AGTR2, IDO1, SLC25A27, ABCG4, CD55, APOA4, MCOLN1, REM1, ATCAY, EBPL, HSPB2, HSPA9, PLK2, GAD1, NANOG, DCX, COASY, UBE2K, DDIT3, TREML2, APBB2, MAP1LC3B, SRRM2, GZMB, FXN, HNRNPA1, HPSE, RAB10, CIP2A, FOLH1, STIM2, DIO2, MMP24, CEBPZ, GBA, CDR2, ITPR3, CDKN2A, MELTF, SLC30A3, ADRA2B, FTO, FNDC5, GGA3, XPNPEP1, VGF, NR1H2, UGCG, MFGE8, MGAT3, CXCR4, TLR9, APOC3, GPT, ELK3, NEAT1, ADORA2A, MMEL1, TRPC6, EIF4E, CAMK2A, MS4A6E, SRR, HSPA14, IRS2, MGAM, C1orf52, HDAC3, PABPC4, ACKR3, LGALS3, FAM20C, WNK1, DRD4, CYP2C9, MBTPS1, DRD1, LRP6, GRK2, CYP2B6, OGT, LIPA, AD11, GORASP1, PTGDS, SPEN, MIR200B, NPTXR, DNMBP, MIR200A, NCOA6, MIR181C, RBP4, RELA, OPN1LW, EFHD2, MIR188, TPH1, HNRNPA1P10, CTNNBL1, SLC40A1, PNO1, CHCHD2, SDF4, RETN, GOLM1, PPP3R1, PYCARD, PAG1, CCR2, DDIT4, RCBTB1, SBNO1, PPARD, CD274, PCBP4, ACE2, PROS1, PRND, PPP1R15A, CIZ1, MIR26B, TPSG1, GGA1, CFAP97, MAP2K1, AATF, SHANK2, PRL, RBMS3, LOC107987479, MAP2K2, PAXIP1, CHCHD10, SBNO2, PTGES, SPHK1, LPAR2, PPIG, NRXN3, MED23, SPP1, MAPK8IP1, BAG3, APBA3, TAP2, PRDX6, CARTPT, SNAP91, SV2A, MALAT1, MAK16, SYVN1, GDF11, TAC1, TAT, SLC6A2, TRPV1, CISD3, TPT1, TSC2, TM7SF2, TXN, UBE2I, TLE1, TIMP2, XK, CNTN2, TGFBR2, YY1, GOLGA6A, ANP32A, TAM, TERT, DCP1B, TNFSF10, PPP1R1B, GPHN, RGS2, ADAM30, SAA1, METAP2, IMMT, SDS, ADAP1, RYR3, ECHDC3, RYR2, RXRA, SCD, RPS6KB1, CIT, RPS6, CTXN3, LMTK2, NLGN1, ROCK1, RGS4, ATXN2, SRL, STUB1, SHBG, LILRB2, AKR1A1, OLFM1, SKIL, SLC9A6, CREB3, PITRM1, SCGN, CXCR6, OCM, RIN3, SGCA, SFPQ, NCKAP1, CPLX2, TP73, EDAR, CCL3, NPS, BEST1, HPS1, CXCL1, GLO1, LIF, CDH1, LHCGR, CDK4, PCNA, PCK1, L1CAM, GPR42, GPX1, GRB2, ANGPT1, ANGPT2, CETN1, MYD88, GLB1, AKT2, LMNA, DNMT3B, TSC22D3, CD38, PER1, CD69, DRD3, LOX, CD74, LMNB1, DNM2, GAS6, AVP, GC, DMRT1, SARDH, GRIN1, ANXA5, BACH1, P2RY1, INPPL1, CSF1, CS, NEFM, NTS, APEX1, STS, HTC2, NEUROD1, NPTX1, NPPA, ATF2, HTR2C, ARRB2, IGFBP7, HMGCS2, CLK1, CKB, APBA2, CYP17A1, GSTM3, CHGA, CYBB, JUN, CTSS, ORM1, ITPR1, CHRM1, CHRM2, OPRK1, OPRD1, CTRL, HK1, ADRB1, LAMP2, CASP2, EDNRA, PLD2, CAPN2, F2RL1, ACO1, ERBB4, FAT1, FGFR3, CALM2, BRS3, CALCA, CAD, EGF, CASP4, FCGR3B, FDPS, LYZ, FCGR3A, FLNA, MECP2, FABP3, ADRA1A, PLXNA2, MBP, FAAH, ENPEP, F12, BAG1, MEOX2, HOMER1, ITGB2, DBA2, ITGAL, ITGB1, AIM2, AZIN2, CD80, ITIH4, CD46, VIP, CHRNA3, ATG5, TREML1, MCL1, GPRASP2, VWF, APOA5, TMEM119, KLF4, SOCS6, WNT1, XBP1P1, FOXQ1, C3AR1, OPN4, USF1, C1QA, CXCR2, VPS26A, MOGAT3, CCR3, IL6ST, IL5, IL1RAP, LMF2, IL1R1, CREB3L1, UNG, MCU, CLSTN3, SNPH, IL9R, NPEPPS, NAPSA, USF2, MEF2A, ING1, CGB8, FTMT, CHM, VAV1, IMPA1, C1R, ILK, ADAMTS3, IL16, MAP3K5, IL15, GDF15, CGB5, CA2, KCNB1, TSPOAP1, SMAD2, DPPA2, SGO1, LIG3, IFNL3, TNK1, CP20, APCDD1, HSD17B6, CDKN1A, TTBK2, CDKN1B, SLC2A14, CFLAR, STMN1, LIPC, TAB3, CHIT1, BRAP, SPARCL1, MLKL, PTCRA, CD47, LGR5, CD8A, CCT, NR4A3, USP9X, MSRB3, CDR3, CCK, LNPEP, CASP7, CHRFAM7A, CAMP, PER3, YES1, CGA, MARK3, CGB3, SYNGR1, CALCR, IL1RL1, ARHGEF2, PER2, SLC33A1, TPH2, CHEK1, RAB7B, NOG, MBL2, CFL2, HSPB6, AHSA2P, SLC30A1, CD200R1, SOCS3, KDR, KIF5A, HAP1, CALR, CES1, TRPA1, HSPB3, WASF1, SLC32A1, ARHGEF7, CAMK4, COL3A1, H3P40, SCRN1, PTCD1, SPHK2, ATN1, PPIL2, POU2F1, FOSB, GCA, FLT4, SH2B1, APPL1, DNMT1, FLG, FOXO1, DUSP1, DUSP6, HHAT, HSPB8, E2F1, PLXNA3, DOCK2, PNPLA2, ADI1, GMFB, GPI, GPC1, KIF21B, NMNAT2, TRIB3, ALS2, DLG2, DLG3, GLS, PDSS2, ASTN2, MCF2L, GLI2, KIDINS220, CBLIF, SYNE1, DMD, GGT1, FKBP1A, SIT1, SV2C, GDE1, FOXP3, ASCC1, TMED7, FIS1, PRLH, CRYL1, ADIPOR1, LSR, F11, MBL3P, SIRT6, TRMO, NRN1, LCMT1, PRRX2, ERN1, BIN2, UBR5, HEBP1, GEMIN4, PDCD4, TBK1, SLC25A38, FGF14, PCSK1N, TRPM7, DLL1, FLVCR1, AHI1, SETD2, ELK1, IL22, NCAPH2, ELN, PADI1, BPTF, NRBF2, FABP5, EP300, PLA2G3, GRHL3, CXCR3, NAV3, SIRPB1, FLOT1, MET, KCNMB2, CRISPLD2, ARHGAP24, HNMT, SNX27, NPL, BHLHB9, TRIM13, HMOX2, KLF2, CSNK1E, LPAL2, CPQ, PPP1R2C, RAPGEF3, TET1, CRYZ, SORBS3, CTBP1, BCL2L11, COL17A1, NCAPD2, COX10, UBASH3B, NR1I3, ACOT8, PTPN5, PPP1R9B, TOM1, MINDY4, CPE, HTR7, NR1H3, HTR1B, HTR1A, LRPPRC, PDIA6, RHBDD1, NAA25, HLA-C, TPX2, BCAN, ADAMTS13, MOAP1, TNMD, GRIA3, NEUROD6, CHEK2, PADI2, HRH3, PHB2, SIL1, MGLL, FFAR1, GADD45A, MMRN1, DEFA1, IL21, NLRC4, GPR17, AZI2, HHIP, CTF1, HCRTR2, HLA-B, CTNND2, HHEX, HGF, CTSG, HDAC1, CTCF, DHX40, PTGES3, STIP1, CTSZ, CXADR, CARD14, CYP1A2, PDE10A, LILRB1, EHMT2, PDIA2, UMOD, ANGPT4, MIR339, SYN2, MSD, ACP3, APEH, ST8SIA1, AZU1, PI4KA, NCAM1, MIR144, SMIM10L2B, MSI1, NAP1L1, PRSS3, PEBP1, MASP1, SIM2, TIA1, MIR15B, ATD, RPL29, ABCC1, NCAM2, MIR125A, TLR5, SERPINF2, TNFAIP1, CXADRP1, MAPK9, ZFHX3, GGTLC4P, AD10, SGCG, MIR451A, CDR1-AS, TPTEP2-CSNK1E, MIR384, ITSN1, CBSL, MPZ, NFATC4, PKM, NCL, NTF4, LOC643387, SLC1A3, APOA2, THAS, PSMB6, SERPINB6, PSMB9, RHOA, ARMCX5-GPRASP2, SMPD1, REG3A, ATP4A, MIR193B, RFC1, NOTCH4, SLPI, PGF, AEBP1, MIR214, MIR219A1, SLC19A1, MIR22, PCSK1, ALPP, AMD1, MTNR1A, TGFBR1, COX3, ATP12A, NM, ADD3, PSD, TGM1, ARR3, NPM1, PAK1, TMED7-TICAM2, PNP, MIR195, MTHFD1, ADH1B, AMPH, ND4, AMD1P2, ARG1, SULT2A1, RRAS, PDE7A, TTPA, TYK2, TXNRD1, PPP1R1A, PPP1R10, SPG7, SPAST, RAB4A, PPP2CA, OTC, PPP2R2B, MMP1, ARMS2, RAB3A, GGTLC3, RTL1, P2RX4, ST13, SPARC, ALAS1, PPP3CA, NEFH, SEL1L, TYR, RAB6A, MICB, PPIA, CCL4, BST1, TICAM2, BNIP3, MIR326, OPRL1, PON3, BMP6, OPRM1, AHSG, H3P17, SDC2, AGRN, TYRP1, PPP1CA, BMI1, TYRO3, PNMT, DEFA1B, GGT2, ORI6, SMIM10L2A, CISD2, ARSA, EIF2AK4, PRKAR1A, LRP1-AS, SRSF2, MIR98, MIRLET7B, CD200, PDCD1, RAP1A, GGTLC5P, CCND1, ANXA6, FXYD1, S100A6, NFATC3, PLK1, ABO, PTGER3, APC, S100A12, ASL, HSP90B2P, SETMAR, PRRX1, PZP, STAT1, ODC1, CFB, CDNF, ZBTB4, PARK16, SUGP1, DIO1, SORCS2, MAGEE1, ALDH1A1, MIR1306, DES, DIAPH1, LSM2, MIR1229, XPO5, HCN3, CFD, MIR664A, KIF17, WDR48, MTRNR2L12, PRX, DHFR, EPG5, SEPTIN1, FAS-AS1, RNF213, MIR320E, MIR1908, HECW2, LINC00672, NUFIP2, ABCD1, DLG1, QRFP, ZNF410, AOC2, NBEAL1, CYP11A1, OPN1MW2, AD6, P2RY12, NMNAT1, DEPTOR, TNS3, CYP2D7, FAM72A, NUCKS1, CLEC7A, CYP26A1, ARAP3, GREM2, CDKN2B-AS1, CYP2J2, UBE2Z, MIR1246, TSPY3, MIR632, CTSK, GTDC1, CTSL, MIR650, MIR660, SNORD118, TNFAIP8L2, LYNX1, MUL1, PAGR1, CYLD, MAPKAP1, APOF, PDCL3, CYP2C19, NOC3L, CYP27A1, DPEP2, MFT2, PROK2, HPSE2, AD14, AKR1C2, ALPI, TRPV4, NTN4, PRM3, PDF, JAM2, ALOX5AP, TSPY10, DEFB4A, DEFB4B, ALOX12, PTBP2, DCN, NECAB3, FKBPL, NEUROG2, DGKQ, SLC25A4, MIR873, MIR301B, CENPK, DAXX, GFRA4, GOLPH3, ERVK-6, MTUS1, DBI, MIR937, ANG, ACE3P, SOD2-OT1, ANK3, DRD2, ZNF608, NAT10, DYM, LOC102724334, TRIT1, EIF4G2, TET2, EIF5, SERPINB1, ELAVL4, PDP1, ACO2, THRA1/BTR, UGT1A1, CCHCR1, CPVL, SMOX, TOLLIP, TERF2IP, SNTG1, EMP1, LOC102723407, EIF4EBP1, MIR6845, EIF2S3, ADCY2, NUDT11, EGR2, MSTO1, ADARB1, SLC6A15, ADA, TAPBPL, TESC, MIR6840, ACVRL1, FOCAD, EIF4A1, CASZ1, QRICH1, PGPEP1, EIF4A2, NDE1, ASIC2, CTTN, ACADVL, GSKIP, LNCRNA-ATB, ATP6V1H, H3P7, TDP2, ERBB2, CINP, ZCCHC17, H3P13, DTL, GPRC5B, ERCC1, DCDC2, NAT8B, GULP1, H3P23, ERG, H3P28, H3P11, PPIL1, STIN2-VNTR, NANS, EPHA8, H2BS1, POLE3, ACACA, SLC29A1, FXYD6, LRP1B, CST12P, SIRT1-AS, INPP5K, MSRB1, ARID4B, EPOR, ABL1, AAVS1, NR2F6, ERVK-32, LOC110366354, MNS16A, EFNA5, SLC47A1, ALAD, EEF1A1, SNHG19, MICA, DNTT, SOX21-AS1, DOCK3, DPYSL3, MIR626, XAB2, MFF, DUSP22, ARNTL2, SPPL2B, MCCC1, TMX2-CTNND1, ANKS1B, DPYSL5, FXYD6-FXYD2, BARHL1, DSC1, TWSG1, TLE5, DNASE1, DNA2, OCLN, NLN, AMIGO1, AHR, PLEKHG5, SLC24A3, SPC25, TTC7A, PELI1, JAG1, TMEM159, RTN4, APMAP, CD177, CAMK1D, PLAAT1, NR0B1, TIGAR, P2RX5-TAX1BP3, PARD3, GKN1, ADH6, INAVA, CDK5RAP2, OGDHL, LINC01080, ATF7IP, IPO9, VAC14, DVL1, PPP4R3A, OPN1MW3, EBM, OTUB1, SOX6, SLC30A10, SMPD3, MEG3, PLIN2, FBXW7, TDP1, ADORA1, DSC3, ACSS2, BTNL2, KIAA1217, ZNF253, CFC1, MIR4668, DSG1, APOM, MYO5C, MIR4487, NOTCH2NLC, USE1, SELENOS, GDNF-AS1, DSPP, ADCY10, ADRA2A, ZNF415, LINC-ROR, NARS2, CSF2RB, MIR616, MIR20A, CDC25C, PROM2, ATP6V1E1, IL23R, GLIS1, PM20D1, PHF13, CDH2, ZNF569, MIR191, CDK9, MIR192, PRIMA1, CDKN2D, MIR196A1, OR2AG1, LAYN, PIWIL4, MIR19B1, GPBAR1, CDC25B, GDF7, ZDHHC15, MIR139, CD63, SGMS2, MIR140, TMPRSS6, RHBDL3, AVPR2, MIR15A, CBLL2, MIR186, PRUNE2, AMOTL1, CD81, MIR18A, SLC2A12, CDA, MIR181A2, ATP5PO, SESN3, ATP6V1B2, UBR1, ATP5PF, PPME1, MIR224, LYZL4, KCNH8, MTERF4, MIR23A, CPO, ACMSD, MIR23B, BHLHE23, MIR25, CFL1, OSCAR, SPNS2, SEZ6, SLC38A10, MSI2, CFTR, MIR27A, MIR223, ALDH7A1, MIR221, SELENOM, ATP5MC2, CACUL1, HECTD2, SREK1, CTCFL, CBLN4, CDSN, ATP5MC1, DEFB104A, OCIAD2, MAGEC3, MIR210, CEACAM5, CECR, PPARGC1B, ATP5F1B, IL31RA, GNPDA2, SCARB2, NSMCE1, SOCS4, UBE2L1, BNC1, CACNA1C, SLC25A20, SERPINA13P, BLM, SREK1IP1, MIF-AS1, C20orf203, SYPL2, ZNF763, CCL4L1, BID, BGN, ZSCAN1, ZADH2, SMIM20, MILR1, PGP, GOLGA6L2, TMEM189-UBE2V1, TMEM189, IL31, C4BPA, BTK, AMIGO2, HCN1, NHLRC2, ATP9B, SBSN, BMP1, OSTN, C5, CFAP410, BARHL2, NANOS3, C9, STING1, GADL1, ARMH1, VPS51, HCAR2, CAPG, LINC00639, TMEM201, LIN28B, CD5L, MIR127, CD19, KIF6, MS4A1, MS4A3, HYLS1, STOX1, FOLH1B, OR8J1, TRIML2, CD28, KHDRBS2, GAPT, CENPV, KLHDC8B, MIR134, CD86, PIKFYVE, SLC29A4, CCNC, KRIT1, PTF1A, DAOA-AS1, BDKRB2, HCA1, BRD3OS, ASPM, BCS1L, SGMS1, BCR, MIRLET7D, MIR122, RUNX1, ANKK1, BCL6, PHYHD1, BAK1, MIR10A, EBF3, CCKAR, MIR28, FRMD6, MIR613, ADAMTS10, TMEM175, XIAP, MAF1, BIRC3, SLA2, ANTXR1, ASCC2, CRHBP, EVA1A, QRFPR, MAGT1, NCALD, LOC646506, ROPN1L, L3MBTL2, GMNC, SCFV, CSE1L, RNF146, PHF6, HOOK3, BRSK1, MBOAT4, COX15, MIR497, MFSD2A, MIR501, ACCS, ARG2, FAM126A, CPB1, CPN1, ECSCR, MAP1LC3A, MIR484, AQP9, CPS1, SNORD35B, CPT1A, ABLIM2, FASLG, NETO1, DOCK8, RNFT2, C1QBP, TM2D3, ASRGL1, PTGES2, PANK2, MIR590, SCD5, CSNK2A1, VCAN, ZC3H14, CSPG4, CTBS, MIR592, MIR598, CAMKMT, CTNS, SLTM, PTCD2, CTNND1, MIR603, NUBPL, WDR26, SPHKAP, GSTT2B, TMEM163, NCF1, LBH, SPAG11A, SFTPA1, CSF3R, ZNF436, CSN2, NDFIP1, MIR545, SLC44A4, SLC19A3, FAM72B, AIRE, IQCJ, CSNK1G2, DNAJC5, CSNK1G3, LINGO1, ATG4C, ATP2B4, MIR346, SERPINC1, CISH, ASPA, CLC, UCN3, TMEM54, ASS1P1, CLCN3, NACC1, ASIP, STX1B, IFT43, MIR133B, MIR151A, CLK2, TP53INP1, MIR330, MIR335, MIR338, MIR93, SLC26A7, OMA1, CHGB, PLD4, TDRD9, CHD1, MIR299, ATIC, ATHS, H4-16, LRIG3, EXOSC6, CHRM3, MIR30B, MIR30E, AGAP2, MIR31, MIR34C, MIR9-1, GRIN3B, GRIN3A, ASAH1, MIR369, H2BC12, KPRP, LRSAM1, MIR429, H4C15, SHF, GADD45GIP1, COL11A1, ZNF628, MIR431, HNP1, NAV2, MIR409, SLC31A1, RPPH1, SNORD14E, SNORD14D, SNORD14C, SNORD14B, COX6B1, MIR485, CNTN1, DNM1P33, CNTFR, CHRDL1, CLN3, MIR361, MYOCD, PRDM6, DNER, SPECC1, MIR377, CLN5, EXOC3L4, CNP, MIR425, ARRB1, ZNF804A, BDNF-AS, NLRP12, CCR6, ABCC2, DEFB104B, LRRC15, POU3F4, HOOK1, TERC, NAT1, MCM2, EZR, MDH1, VEGFC, MDH2, MDM4, MEF2D, UVRAG, UROD, UQCRC1, UGT1A, SLC35A2, UCP2, UBTF, UBP1, MID1, UBE3A, UBE2V1, CXCL9, ATXN3, UBE2D2, UBE2A, UBC, MAP3K10, MC1R, WARS1, WAS, ZMYM2, MANF, SCG2, FZD5, SMAD7, MAG, MAP3K12, MAP1A, MAP1B, ZNF236, ZNF224, ZNF217, RNF112, WEE1, MZF1, ZIC1, MARS1, MAS1, MAT1A, MAT2A, MAZ, XIST, WT1, WNT2B, WNT5A, UBA52, KMT2A, MLLT3, THBS1, TLR3, TLE3, MSH3, TKT, TIMP4, TIMP3, MSR1, MSRA, THRA, THOP1, THBS4, CYTB, MRE11, NUDT1, TGFBI, TGFB3, ND1, TFF3, TFDP1, MTNR1B, MTRR, TRNL1, MUC1, TERF2, TSPAN7, MRC1, TWIST1, TRAF2, TUBA4A, NR3C2, TTN, TSPY1, TSHR, TSG101, TSC1, MMP7, MMP8, TRPC1, TRH, NR2C2, TNFAIP6, MMP13, TPM1, MOG, MOV10, TP53BP2, TP53BP1, MPG, TNR, TNNI3, MPI, MPST, SLBP, REEP5, DEK, SNX3, TNFRSF6B, RAB11A, LDHA, LEPR, LGALS4, LGALS9, GPAA1, RNMT, GBF1, ADAM19, URI1, TRADD, LCK, B3GALT4, LIFR, LIG1, SOCS1, NUMB, LIMS1, AOC3, PDE8B, USO1, TNFSF11, STK16, LCT, CES2, KMO, KLRC1, BRSK2, KCNQ1, KIR2DL2, NOL3, ATP6V0E1, SELENBP1, USP13, KLKB1, CDK5R2, RAB29, MBD2, KIF11, TMEM11, ENDOU, EIF2S2, TAX1BP1, NAE1, KRT14, KRT18, LAMC1, LBR, PROM1, LCAT, SOCS2, PRKRA, DEGS1, DDX39B, PABPN1, EOMES, BAP1, LTF, H4C9, COLQ, DYSF, CHAF1B, LYN, NRIP1, COIL, SLC7A5, AD5, H4C1, FGF23, ADAM12, BRD3, PSCA, ARHGEF5, TFPI2, FZD3, GHS, M6PR, MARCKS, SMAD1, LTC4S, H4C4, BHLHE40, IRS4, MAPKAPK5, LMO4, LOXL1, CST7, DDO, DGKZ, GAS7, PIK3R3, PKP4, PPFIA1, LRPAP1, SORBS2, H4C6, CUL4A, GNPAT, LTB, H4C14, H4C13, H4C5, H4C2, H4C8, H4C3, H4C11, H4C12, TERF1, MUC4, KCNMA1, TDO2, PCP4, CDK18, RBM3, RBL2, RBBP6, RB1, RASGRF1, RASA1, RARRES2, RAN, RAF1, RAD52, PCYT1A, RAD23B, RAC2, PDB1, RAB27B, RAB27A, PDC, PDE2A, PURA, PDGFB, ENPP2, PDYN, PTPN13, PC, PAX6, PARN, RPL15, P2RX1, S100A8, P2RX3, P2RX5, P2RY4, RREB1, RPS23, RPS21, RPS6KB2, P2RY6, RPS3A, RPL13, RET, RPA1, PAFAH1B2, RORA, ROM1, SNORD15A, BRD2, RNASE1, RHO, RHD, PAK3, TRIM27, PTPN11, PENK, PTN, PMM2, PLAUR, PLCL1, PLEK, PRKCE, PRKCD, PLP1, PRKAR1B, PRKACB, PRKACA, PLXNB1, PML, PRG2, PLAT, PMP22, PRB1, PPT1, PPP2R5E, POLG, PPP2R1A, PPP1CB, PPL, PPIC, PPIB, POR, MAP2K3, PLAG1, PFDN5, PSMD2, PFKFB3, PTGER2, PTGER1, PGD, PTGDR, PTCH1, PGR, PHB, PSMD9, PSMD7, PSMD3, PSMB2, PITX2, SERPINE2, SERPINI1, KLK10, PIK3C3, PIK3R1, KLK7, PIK3R2, PRS, PROS2P, PIN4, PROC, S100A10, OXT, OXA1L, SQLE, STAR, ST14, ST2, NDUFA6, SSTR3, SSTR2, NDUFA9, NDUFB8, SRM, SRF, NEDD4, SEPTIN2, STC1, SP4, NEU1, SOX5, SOX3, SOS2, SOS1, SOD3, NFE2L1, NFKB2, SNRPG, SNRNP70, NDUFA5, STIM1, NME1, MYH9, TRBV20OR9-2, TCP1, TCN2, MMUT, MUTYH, TCF4, ELOC, TBX2, MX1, MYH6, TARBP2, MAP3K7, STK11, MYO6, TACR2, NACA, VAMP2, VAMP1, SURF1, ABCC8, SUOX, NDP, STXBP1, STX1A, NINJ2, NME2, SAA2, OMP, SFTPC, TRA2B, SRSF6, SRSF5, SRSF3, SRSF1, SFRP1, OCA2, MAP2K4, ODF1, SELE, OPA1, OAS3, CXCL11, CCL21, CCL20, CCL19, CCL8, CCL1, SCP2, SCN1A, ORM2, OSM, TSPAN31, OAT, SGSH, SUMO2, SLC8A3, SMPD2, SLN, SLIT3, SLC22A5, SLC22A2, NQO2, SLC18A1, SLC16A1, SLC12A3, SLC11A1, SLC10A2, SLC8A1, NUP98, SLC6A12, NPHP1, SLC6A1, SLC5A2, NRCAM, NRDC, SLC1A1, NRF1, PMEL, YBX1, NT5E, NAT8, SEMA5A, ESRRA, RAB31, MACF1, HEY2, BRD4, TRAM1, CBX5, ANGPTL2, OPN1MW, GRIP1, KCNH4, MSTN, GFER, GFRA1, SIRT5, COTL1, GFRA3, GHR, ZNF629, UBR4, GHSR, WASHC4, GLI1, NUP160, CLUH, GLI3, SCFD1, KCTD2, CLCF1, SEC14L2, NR5A1, SLC24A2, PRPF6, TFIP11, MAFF, EID1, RAB38, FSHR, TMEFF2, PLA2G15, SLC7A11, FTH1, SNHG1, TSPAN15, GAST, ACKR1, G6PD, GAB1, NTSR2, GABBR1, GAD2, GALNS, DDAH1, PADI4, GART, NBEAL2, GMPR, PLEKHM2, WDHD1, GPR39, CARD8, ARHGEF15, AAK1, SYNPO, GPX4, ECD, PARK7, KLF8, TREX1, WIF1, WDR45, ATF6, CORO1A, TBC1D8, SLC7A9, GRIA4, FAF1, GRIK4, RER1, GRM1, STMN2, RAPGEF4, ADRM1, MSRB2, RAB3GAP1, GNA12, ZNF423, ATG4B, UBXN4, RCOR1, SEPTIN8, STAB1, GNAI1, MAPK8IP3, GRAMD4, GNB3, NFASC, KIF1B, GOLGA2, GPER1, SETX, GOLGA4, PDZD2, SAMD4A, KDM1A, GPM6A, RAB21, GPR6, P2RX2, GPR20, SNW1, FRK, FBXO7, BRI3, SNX12, SOCS7, CD209, FABP6, TBX21, NOP53, FABP7, SLC2A8, UBQLN2, A1CF, PSAT1, FANCG, HOOK2, DELEC1, FASN, SNX8, NPC1L1, BLNK, MS4A2, FCGR1A, FCGR2A, MYLIP, SCG3, DROSHA, TMEM230, NOX4, PCA3, SPCS1, VRK3, ETFA, SLC25A37, TLR8, SLC22A17, ECSIT, CD320, EZH2, DNAJC27, CLEC1B, NT5C3A, MZB1, F2RL2, HP1BP3, F3, F9, IRAK4, SAR1B, UTP11, F13B, SH3GLB1, SIDT2, SHANK1, TRAT1, F11R, RGCC, TMEM176B, NOCT, FBXO2, NPTN, TPK1, VCX, GREM1, FKBP1AP2, FKBP1AP3, AGO1, SEZ6L2, FKBP1AP4, FGF21, CLDN17, NOC2L, SND1, FOXM1, EPC2, ATRNL1, LRP10, FLNB, FMR1, POU2F3, TXN2, FBXL2, FOLR1, FOLR2, FKBP1AP1, B3GAT1, IGHV1-68, TNFRSF21, FEB1, FES, FGF9, RABGEF1, PRPF19, FGF13, FGFR1, FGFR4, PDLIM3, RND1, KLHL20, COQ2, CACYBP, HCAR1, FHL2, VPS4A, IL37, GLS2, NAAA, CYTH4, DKK2, DKK3, BBC3, SDCBP2, GRM3, IL24, SPAG9, CXCL2, PCLAF, IGFBP1, ACAP1, IGFBP5, SART3, KDM4A, IGHG3, SDC3, SH3PXD2A, RGS6, SNCAIP, TCL1B, IL4R, IL7, BCAR1, CCL4L2, CXCR1, BAG2, IL12B, BAG5, TMEM59, TBPL1, GAL3ST1, AKAP5, STX8, PIEZO1, BMS1, PTDSS1, IDH1, SH2D3C, GNE, SH2B3, IRF8, SRA1, TANK, KCNE3, HNRNPDL, CCS, NUP153, MED12, HS3ST1, TOMM20, RBM8A, IDH2, CFI, SV2B, TECPR2, IFI27, TOMM70, KIAA0319, IFIT3, IFNAR1, IGBP1, INSRR, PCYT1B, IL27RA, CCNE2, NOLC1, TIAF1, JUND, ZMYM3, KCNC4, KCNJ13, HGS, SYNGR3, ATG12, CBFA2T2, RABEP1, P2RX6, RAB11B, SLC16A3, SLC16A4, ATP6V0D1, RGN, USP10, USP2, USP14, DNAJA3, CLDN1, CLDN8, ARTN, JUNB, GPR50, PICK1, ITPKB, IRAK1, HOMER2, IREB2, IRF3, IRF6, IRF7, ITGAV, CYP7B1, ITGB3, NRXN1, SLC22A8, ITPR2, AIMP1, JAG2, ITGBL1, LHX2, SLIT2, TAOK2, CD163, JAK2, GPR37L1, PIWIL1, MAPKAPK2, PDLIM7, IARS1, TNC, IL18BP, CCT2, HCK, NRG3, USP39, DCTN6, CD226, HDC, HDLBP, CAMKK2, HIP1, TXNRD2, NPC2, SLC35A1, HBG2, PRDX4, ZNRD2, HYOU1, HLA-DQA1, SEMA4D, HLA-DQB1, NXF1, HLA-DRA, ATP5PD, COG5, GPNMB, CHL1, HAS3, FAM3C, GYPA, GSK3A, COPS5, GSM1, GSTM2, EBNA1BP2, PRSS21, PRDX3, GSTZ1, GTS, GUSB, C1QL1, GYPB, HAS1, GYPC, CCL27, ALDH1L1, GYPE, HAGH, WASF3, HSPH1, GJB6, HARS1, ARPP19, DHS, HLA-DRB4, HLA-G, PQBP1, MPHOSPH6, STAM2, GLYAT, HOXA@, RABEPK, HPCA, CALCOCO2, HRC, OLIG2, DDX39A, TOPORS, EIF1, HSD17B1, RAMP2, WASF2, HSD17B4, HSPA2, HSP90AB1, DNAJB1, NAMPT, BCAP31, CTDSP2, TSPAN3, ACTR2, CERT1, ABCC4, HNRNPK, HMBS, NPM3, CFDP1, PRMT5, HMGB2, YAP1, IFITM3, SPAG11B, PEMT, RACK1, SYCP2, TUBB4B, SEMA3A, WARS2, HNRNPC, FOXA1, CCL26, TLR6, FOXA2, LAMC3, LANCL1, HNF4A, TCIRG1, APBB3, APC2, HNRNPA2B1, MTCH2
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Sensorineural Hearing Loss
Wikipedia
More than 40 genes have been implicated in the cause of deafness. [2] There are 300 syndromes with related hearing loss, and each syndrome may have causative genes. ... The most common cause of recessive genetic congenital hearing impairment in developed countries is DFNB1 , also known as Connexin 26 deafness or GJB2 -related deafness. The most common syndromic forms of hearing impairment include (dominant) Stickler syndrome and Waardenburg syndrome , and (recessive) Pendred syndrome and Usher syndrome . ... The hearing loss in this condition is often ANSD (auditory neuropathy spectrum disorder) a neural cause of hearing loss. Muckle–Wells syndrome , a rare inherited autoinflammatory disorder, can lead to hearing loss. ... Congenital [ edit ] Infections: Congenital rubella syndrome , CRS, results from transplacental transmission of the rubella virus during pregnancy. ... Abnormal development of the inner ear can occur in some genetic syndromes such as LAMM syndrome (labyrinthine aplasia, microtia and microdontia), Pendred syndrome , branchio-oto-renal syndrome , CHARGE syndrome GATA2 deficiency , a grouping of several disorders caused by common defect, viz., familial or sporadic inactivating mutations in one of the two parental GATA2 genes .GJB2, SLC26A4, MYH9, GJB3, TMC1, LHX3, COL2A1, LRP2, SOX2, COL11A2, DMXL2, RNF13, COL9A1, ABHD12, FGF3, ACTB, IRX5, LRTOMT, YME1L1, EDNRB, FADD, GLIS3, EIF3F, RIPOR2, KCNJ10, PTGDS, SLITRK6, EYA4, PRPS1, GJB6, BSND, CAT, WFS1, COCH, SLC7A8, ATP6V1B1, ATP1A1, ATP1B1, SLC12A2, SOD2, IGF1, OPA1, TECTA, MYO15A, OTOF, GATA3, MYH6, USH2A, GIPC3, ATP1A3, RNR1, COQ6, HARS2, DIAPH1, CLCNKB, STRC, NLRP3, MYO7A, SOX10, BCS1L, SLC4A11, CEP250, COL4A5, CDH23, TMPRSS3, PMP22, KARS1, USH1C, PTPN11, TRNS1, BCAP31, GATA2, DNMT1, DLX5, ZMPSTE24, VPS13B, PCARE, FGFR3, MRPS2, PCDH15, GRHL2, POLG, ERCC2, PDZD7, PTRH2, FKBP14, PEX1, SLC52A2, HOMER2, PRKCB, TBC1D24, TP63, SMPX, NDP, SLC52A3, KMT2D, WHRN, MITF, RPE65, XPA, IARS2, SPATA5, BTD, COX2, SIX1, OTOA, PAX3, KDM6A, CLRN1, RERE, NIPBL, SLC17A8, PNPT1, ILDR1, RAF1, LMNA, LMX1A, FGFR1, GRAP, THRB, GFER, TBL1Y, COX8A, GJA1, CHD7, COL11A1, TFAP2A, TRPV4, ABCC9, DNM1L, TOPORS, NR2E3, SEMA3A, PRPF8, ARHGEF18, YAP1, CNOT1, ARSG, FASTKD2, DOLK, MRAS, LDB3, PRDM5, PRSS23, PNPLA6, SNRNP200, AMMECR1, STAG2, POGZ, PPIP5K2, EBP, TXNRD2, SLC19A2, SMCHD1, SPTLC1, NEBL, CIB2, SEMA3C, CAP2, COG5, MERTK, MED12, AARS1, RBM8A, MAFB, XPC, MOGS, SEM1, CSRP3, AAAS, IFT88, GDF5, LZTR1, SMC1A, FZD4, OFD1, PEX3, KCNAB2, CDC14A, TCAP, WNT10B, CLIP2, BEST1, TPM1, NKX2-1, TMPO, TNNC1, TNNI3, TNNT2, TOP3A, TTN, VHL, TUB, TULP1, TWIST1, TYR, SLC35A2, VCL, CASK, DCHS1, CD164, BAG3, SNAP29, LONP1, PLAA, HS6ST1, PEX16, CYP7B1, GTF2IRD1, NOG, IFT140, DHX38, PTDSS1, OSBPL2, ARNT2, MFN2, S1PR2, LRAT, PEX11B, AP1S2, SUCLA2, HESX1, FGF17, PROM1, ST3GAL5, SGPL1, PHOX2B, AIFM1, BTRC, TAF1A, BAZ1B, EXOSC2, PRPF4, PRPF3, SMC3, MLXIPL, CRB1, COX14, COA8, COL25A1, ZNF469, KISS1R, MYPN, LOXL3, SERAC1, NEXN, CEP78, NLRP12, RFT1, NDUFAF2, CDHR1, REEP6, PRRT2, COX20, FAM161A, ARL6, HAAO, ZNF408, SEMA4A, ROBO3, FTO, ALG12, NDUFAF5, FAT4, PPCS, DHDDS, ADGRV1, DCAF17, NUBPL, SLC44A4, DIAPH3, SBF2, SPRY4, ESPN, CATSPER2, TTC8, USH1G, AGRN, SUMF1, TPRN, EYS, NDUFS7, KIF7, CERKL, SLC26A5, CEACAM16, TMEM132E, FEZF1, MIR96, CISD2, PJVK, PRCD, PET100, DUX4, CCDC141, RBM20, SEMA3D, UBR1, SPNS2, MICOS13, NDUFA11, SYT2, PROKR2, TANGO2, ZNF513, HGSNAT, A2ML1, RDH12, CCBE1, AQP4-AS1, CCDC50, C8orf37, TRPV3, XYLT2, PERP, PRDM16, NDUFAF1, RRM2B, ATP6V0A4, IMPG2, TBX22, SOST, MAP3K7, ABHD5, TACO1, TMCO1, TIMMDC1, MBTPS2, DCDC2, SUFU, RAB23, MAP3K20, CLIC5, SCAPER, GMPPA, GMPPB, NDUFAF4, SLC39A14, KAT6B, CLDN14, ARL2BP, FLRT3, PRPF6, FSCN2, NDUFAF3, NSMF, PRPF31, IFT172, PTPN22, TBL2, ANKRD1, COQ2, TSPEAR, NDUFB11, ELMO2, SLC7A14, GJC2, SALL4, PRR12, ARID1B, HACE1, KIAA1549, GBA2, EPG5, IL17RD, GATAD1, NLRC4, EPS15L1, SLC5A7, AGBL5, PROK2, TRAPPC11, PNPLA2, TWNK, DIABLO, ANKH, AHI1, BCOR, SETD5, SLC29A3, FOXRED1, POMGNT1, PIGV, PEX26, WDR11, SPATA7, VPS11, KIZ, TMEM126B, HDAC8, KLHL7, TAZ, VAMP1, TACR3, GUCY2D, HARS1, HLA-DPA1, HLA-DPB1, HOXA1, HOXA11, HOXB1, HSD17B4, IDH3A, IDH3B, IDUA, IGBP1, IMPDH1, ANOS1, KCNH1, KRAS, HSD17B10, GUCA1B, GPC4, GTF2I, FGFR2, FHL2, FOXC1, FOXI1, FOXE3, FLNA, FLNB, FRG1, GAB1, GABRD, GALE, GDNF, GLA, GLI3, GNAS, LAMA4, LIMK1, LMX1B, LORICRIN, ND5, ND6, TRNE, TRNF, TRNH, TRNI, TRNK, TRNL1, TRNN, TRNP, TRNQ, TRNS2, TRNV, TRNW, MYBPC3, ND4, ND3, ND2, MET, LRP4, LRP5, ABCA4, MAK, MAN2B1, MEOX1, MGAT2, ND1, KITLG, KMT2A, MPZ, ATP6, COX1, COX3, FGF8, FKTN, MYO9A, CCND1, BMP4, BRAF, BTK, CA4, CACNA1A, CD151, CDC42, CHAT, CHN1, CKMT1B, ERCC8, CLCNKA, CNGB1, CNGA1, COL4A3, BCR, BBS2, FBN1, ATRX, ACOX1, ACTC1, ACTN2, ACVR1, ACY1, AHR, FAS, AQP4, ARHGDIA, ARL3, ASAH1, ASCL1, ATP1A2, ATP6V1B2, ATP6AP1, COL9A2, COL9A3, COL13A1, COX6B1, DUSP6, ECE1, TYMP, ECHS1, EDN3, EFNB1, ELN, ERCC1, ERCC3, ERCC4, ERCC5, ERCC6, ESRRB, MECOM, EYA1, DSG2, DNASE1L3, DMP1, CTLA4, COX10, COX15, CRKL, CRX, CRYAB, CRYM, DAB1, DMD, DCC, DDB2, DES, DGUOK, DHCR7, DLX6, MYH7, MAF, PRTN3, SIX6, RAD21, PDE6G, RAP1A, PDE6A, PCNT, PAX2, OTX2, RAP1B, RASA2, TNFRSF11B, PDGFRB, RBP3, PRPH2, REST, RET, RFC1, RFC2, RGR, RHO, RIT1, PDE6B, PDK3, PIK3R1, PEX13, POLD1, PHYH, PGM3, POLR2F, PEX14, MAPK1, MAP2K1, DNAJC3, PSEN1, PEX12, RAC1, PSEN2, PEX10, PEX7, PEX19, PEX6, ENPP1, PEX2, PEX5, ALDH18A1, RLBP1, NRTN, ROM1, SNAP25, SLC18A3, SLC25A1, NDUFS4, NDUFV1, NDUFS3, NDUFS2, NDUFS1, SNAI2, NDUFB10, SOS1, NRL, SOS2, NDUFB9, NDUFB3, NDUFA6, NDUFA1, NAGA, SOX3, STXBP1, SURF1, NDUFS6, NDUFS8, NDUFV2, NEK2, NRAS, NOTCH3, RP9, RP1, RP2, RPGR, RPL10, RPS6KA3, RRAS, SAG, SALL1, SCN1A, NF2, SCN5A, SCO1, SDHA, SGCD, NEU1, SKI, PLN, KCNQ4, MYO6, GSDME, MPZL2, KCNQ1, GPSM2, OTOGL, MYO1A, MYO1C, F11, MYH2, CDK5RAP2, SERPINB6, TBL1X, GJB1, GH1, ATOH1, PTCRA, B3GALNT2, MYO1F, CXCR6, ACKR3, SLC35G1, B2M, TRS-AGA2-3, BDNF, TMTC2, CKAP4, TUBB2A, SLCO6A1, SLC9A1, SLC6A8, BRS3, ATP2B2, SLC4A1, RBM45, COG4, MTHFR, RUNX2, SDHD, NOP56, CDKN1C, CDKN2A, CDKN2D, UVRAG, SNRPD1, TNF, IMMT, KLHDC8B, MTCO2P12, ABR, ACADVL, LINC00273, TRBV20OR9-2, ACTG1, DFNA54, IKZF2, GRXCR1, TFAP2B, ADCYAP1, DFNB40, ADRA1A, ADRA2B, JAG1, THOP1, AK2, GSTK1, DFNA42, ABCD1, APOE, CDKL5, AQP2, SSTR4, H19, TK2, TMIE, NEUROG1, LARS2, NEUROD1, NFATC4, MMP3, PRL, HPT, EDNRA, ESRP1, EPHA2, HLA-DRB1, HLA-DQB1, ANO1, HGF, PTN, PTGS2, NTN1, GSTM2, F5, F9, LDAH, VWF, CLDN9, FGF2, GSTM1, GRM7, POU4F3, FOXF2, POU3F4, GPR42, LPAR2, MLANA, GLRX, MSC, TGM5, MEPE, MYO3A, RIPK1, IL1B, PDE5A, SERGEF, EHF, MARS2, COL4A4, NFKB1, NGF, DESI1, CHRDL1, NOS3, AKR1A1, TSFM, NT5E, NTF3, LGALS1, RFX3, RFX1, GPR143, OGDH, TIMM8A, DFNX3, DFNB20, KIT, REG1A, RDX, SCO2, KCNE1, NPL, ATN1, IL23A, H3P13
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Choreoathetosis
Wikipedia
It is a symptom of several diseases, including Lesch–Nyhan syndrome , phenylketonuria , and Huntington disease and can be a feature of kernicterus (rapidly increasing unconjugated billirubin that cross the blood-brain-barrier in infants). ... External links [ edit ] Classification D ICD - 10 : G25.5 ICD - 9-CM : 333.5 DiseasesDB : 16662 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 sclerosis This medical sign article is a stub .PRRT2, FRRS1L, NKX2-1, HPRT1, KCNA1, ATP1A3, APTX, ST3GAL5, OPA3, SLC30A9, NUP62, PIGN, PIK3R5, SETX, PNKP, XPR1, TUBB4A, KMT2B, NDUFA13, PIGQ, AP1S2, CASK, XPA, SYT1, PNKD, ADAR, PIGP, GTPBP2, ARX, SIK1, NADK2, MICOS13, PNPT1, TRIM8, CLPB, DCAF17, PANK2, SLC25A22, NDUFAF5, MRPS34, IRF2BPL, GUF1, GJC2, ELP2, ATM, SUOX, STXBP1, CDKL5, KCNQ3, SPR, IREB2, HSPD1, HSD17B10, GNAS, GNAO1, GCH1, GCDH, FTL, ERCC6, ERCC2, ATN1, DLAT, DDC, CACNA1C, CACNA1B, ATP1A2, KCNQ2, SLC25A42, PDHA1, PURA, QDPR, POLG, PLP1, MECP2, NEUROD2, NDUFA9, SCN2A, SCN8A, NDUFA1, MMUT, ATP6, SLC2A1, MIPEP, PTS, CACNA1A, FSIP1, LRP2, TOR1A, GLDC, PDE10A, MCF2L, KCNA5, ATP8A2, KCNA6
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Hystrix-Like Ichthyosis With Deafness
Medlineplus
Because the GJB2 gene mutation identified in people with HID also occurs in keratitis-ichthyosis-deafness syndrome (KID syndrome), a disorder with similar features and the addition of eye abnormalities, many researchers categorize KID syndrome and HID as a single disorder, which they call KID/HID.
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Chromosome 22q13 Duplication Syndrome
Omim
A number sign (#) is used with this entry because of evidence that this hyperkinetic neuropsychiatric disorder is caused by heterozygous interstitial duplication in chromosome 22q13 (Chr22:49.5-49.7 Mb, NCBI36) involving the SHANK3 gene (606230). Clinical Features On the basis of the phenotype of Shank3-overexpressing mice (see ANIMAL MODEL), Han et al. (2013) hypothesized that SHANK3 overexpression may have a role in hyperkinetic neuropsychiatric disorders in humans. Han et al. (2013) sought and identified 2 patients with small duplications within chromosome 22q13 involving the SHANK3 gene. One patient was an 11-year-old girl diagnosed with ADHD, combined type, who also had developmental delays and learning problems, kleptomania, destructive behavior, auditory overstimulation, and hyperphagia. She experienced 2 generalized tonic-clonic seizures at the age of 2 years without associated fever or other precipitants.
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Autosomal Recessive Cutis Laxa Type 2
Orphanet
The spectrum ranges from patients with classic autosomal recessive cutis laxa type 2 (ARCL2, Debré type) to patients with a milder form of the disease, wrinkled skin syndrome (WSS). Epidemiology Around 40 patients with classic ARCL2 have been reported so far. ... Mutations in the PYCR1 gene have recently been identified in patients with ARCL2 and in patients with a phenotype (wrinkly skin, osteopenia and progeroid features) overlapping with classic ARCL2 and WSS, and the closely related syndromes, gerodermia osteodysplastica (GO) and de Barsy syndrome (DBS; see these terms).
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Glutaryl-Coa Dehydrogenase Deficiency
Orphanet
Differential diagnosis includes encephalitis, Reye's syndrome, familial infantile bilateral striatal necrosis, familial megalencephaly, postencephalitic Parkinsonism (see these terms), dystonic cerebral palsy, battered child syndrome with chronic subdural effusions, sudden infant death syndrome and vaccine induced brain-injury.
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Head And Lateral Line Erosion
Wikipedia
Effects of full-stream carbon filtration on the development of head and lateral line erosion syndrome (HLLES) in ocean surgeon. . ^ http://microcosmaqx.typepad.com/jay_hemdal/2009/02/hlle-survey.html ^ "Mastering Freshwater Aquarium Ecosystems" . Tony Griffitts (2012) . aquaworldaquarium.com. v t e Fish diseases and parasites Pathogens Aeromonas salmonicida Nervous necrosis virus Columnaris Enteric redmouth Fin rot Fish dropsy Flavobacterium Hematopoietic necrosis Heterosigma akashiwo Hole in the head Hypodermal and hematopoietic necrosis Infectious pancreatic necrosis Koi herpes virus Mycobacterium marinum Novirhabdovirus Pfiesteria piscicida Photobacterium damselae ssp piscicida Salmon anemia Streptococcus iniae Spring viraemia of carp Taura syndrome UDN VHS White spot Yellowhead Parasites Abergasilus Amoebic gill disease Anisakis Carp lice Ceratomyxa shasta Clinostomum marginatum Dactylogyrus vastator Diphyllobothrium Cymothoa exigua Eustrongylidosis Epizootic ulcerative syndrome Flukes Glugea Gyrodactylus salaris Henneguya zschokkei Ich (freshwater) Ich (marine) Kudoa thyrsites Lernaeocera branchialis Microsporidia Monogenea Myxobolus cerebralis Myxosporea Nanophyetus salmincola Pseudorhabdosynochus spp.
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Hyperreflexia
Wikipedia
But hyperreflexia can be developed via many other causes, including medication and stimulant side effects, hyperthyroidism , electrolyte imbalance, serotonin syndrome , severe brain trauma, multiple sclerosis, Reye syndrome , and preeclampsia . ... External links [ edit ] Classification D ICD - 10 : R29.2 ICD - 9-CM : 796.1 MeSH : D012021 NIH/Medline Diseases Database (DDB): 20760 Arch Phys Med Rehabil v t e Symptoms and signs relating to movement and gait Gait Gait abnormality CNS Scissor gait Cerebellar ataxia Festinating gait Marche à petit pas Propulsive gait Stomping gait Spastic gait Magnetic gait Truncal ataxia Muscular Myopathic gait Trendelenburg gait Pigeon gait Steppage gait Antalgic gait Coordination Ataxia Cerebellar ataxia Dysmetria Dysdiadochokinesia Pronator drift Dyssynergia Sensory ataxia Asterixis Abnormal movement Athetosis Tremor Fasciculation Fibrillation Posturing Abnormal posturing Opisthotonus Spasm Trismus Cramp Tetany Myokymia Joint locking Paralysis Flaccid paralysis Spastic paraplegia Spastic diplegia Spastic paraplegia Syndromes Monoplegia Diplegia / Paraplegia Hemiplegia Triplegia Tetraplegia / Quadruplegia General causes Upper motor neuron lesion Lower motor neuron lesion Weakness Hemiparesis Other Rachitic rosary Hyperreflexia Clasp-knife responseABAT, ATXN7, TTPA, PMP22, CHRNB2, CYP7B1, UBE2T, COQ2, HTRA2, PCLO, SETD2, NDUFAF4, TBK1, PYCR2, GMPPA, PSAT1, SCAPER, KCNK4, UQCRQ, CYFIP2, TBL2, BSCL2, SACS, HIBCH, IFT172, PRPF31, ABHD12, AUTS2, CHMP2B, PARS2, NDUFAF3, TMEM186, COG4, ATXN10, FSCN2, IMPG2, EXOSC3, DSTYK, ATP8A2, LINS1, RFWD3, DARS2, MTPAP, ANO10, FANCL, NSUN2, GDAP2, VPS13C, NDE1, AHI1, GTPBP2, TMEM106B, TREM2, ERAP1, ATL1, WWOX, ZFR, LIPT1, SPG21, REEP2, PCDH12, UBAP1, GLRX5, TACO1, CHCHD2, RLIM, MECR, MLXIPL, NDUFA13, FBXO7, PRPF6, TBX4, KIF1C, FARS2, ERLIN1, PRPF8, NOP56, MERTK, MAD2L2, WARS2, TFG, APC2, SIGMAR1, STUB1, GPHN, TOPORS, ALG3, PQBP1, HUWE1, NR2E3, KIF14, AP5Z1, WASHC5, RUSC2, DNAJC6, DHX38, MATR3, FRMPD4, IFT140, RUBCN, CEP135, GTF2IRD1, AP4B1, WDR4, FANCI, PNPLA6, NUP62, ARL2BP, PIGN, AP4E1, CRB1, ATP13A2, ARHGEF18, RPGRIP1L, NCAPD3, BICD2, DDHD2, DENND5A, PLCB1, PMPCA, ANKLE2, NFASC, SPART, SETX, SNRNP200, CEP152, NT5C2, RAB3GAP1, PARK7, CHP1, ERLIN2, AP4S1, POLR3A, CIT, CLP1, VPS13D, ELP2, ZNHIT3, RFT1, ZNF513, CPT1C, WDR81, MTFMT, TTC8, ISCA2, TRAPPC6B, LRRK2, TOE1, SLC46A1, MARS2, REEP6, CDHR1, NDUFAF2, C12orf65, NDUFAF6, TMEM67, GFM1, ALG2, WDR73, ATAD1, MFSD2A, GPT2, FAM126A, NKX6-2, SLX4, RNASEH2C, FAM161A, ARL6, BRIP1, GLYCTK, HGSNAT, MAP11, JMJD8, OCLN, PET100, PRCD, ATXN8, SDHAF1, CCDC88C, ALG11, PCARE, CERKL, NDUFS7, TUBB2B, EYS, TGM6, SLC6A19, UBAC2, RDH12, WDR62, ASPM, NALCN, BRAT1, SAMD9L, C9orf72, VWA3B, IBA57, ARX, SASS6, C8orf37, SIK1, IL23R, TTBK2, JAM3, C19orf12, ISCA1, MCCC1, TRMT5, CC2D2A, KIDINS220, MYORG, SCYL1, JPH3, MCOLN1, GJC2, KNL1, RARS2, COQ9, COQ8A, PRDM8, MFF, INPP5E, CLPB, KLHL7, NDUFA12, KIZ, CENPJ, SPATA7, CDK5RAP2, CCDC88A, POLR3B, VAC14, PEX26, POMGNT1, FOXRED1, SLC29A3, CWF19L1, KIAA1549, ALS2, FANCM, GBA2, DDHD1, SLC19A3, CEP63, NUBPL, SPG11, OPA3, PGAP1, PANK2, DHDDS, TCTN2, ZNF408, ALG9, SLC25A22, NARS2, PALB2, MCPH1, NDUFAF5, MRPS34, REEP1, PINK1, NSD1, SEMA4A, IRF2BPL, IFIH1, SLC39A8, MCCC2, TRAPPC11, AGBL5, SLC7A14, PEX16, COPB2, TRIP12, GRIN1, IL12A, IL10, IGHMBP2, IDH3B, IDH3A, HSPD1, HRAS, HPRT1, HLA-B, HEXB, HTT, GUCA1B, GTF2I, GRM1, GRN, FUS, GNAQ, GM2A, GLUL, GLRB, GLRA1, GLDC, GCLC, GJA1, GCSH, GCH1, GBA, GARS1, GAMT, B4GALNT1, IMPDH1, IREB2, ITPR1, KCNA1, NDUFA4, NDUFA2, NAGA, TRNW, TRNV, TRNL1, TRNK, ND6, ND5, ND4, ND3, ND2, ND1, ATP6, ATXN3, MEFV, MECP2, MAT1A, MAPT, MAN2B1, MAK, LMNB1, LIMK1, L1CAM, KRAS, KIF5A, KCNJ6, KCND3, KCNC3, GAD1, FTL, NDUFA10, BBS2, COX10, CNGA1, CNGB1, CCR1, TPP1, CDK6, CACNA1E, CACNA1A, CA8, CA4, C4A, BRCA2, BRCA1, BCS1L, AUH, FANCG, KIF1A, ATRX, ATP6V1A, ASNS, ARSA, ARL3, FAS, AMT, AMPD2, AHR, ADCY5, ADAR, ACOX1, ABCA4, COX15, CRAT, CREBBP, CRX, FANCF, FANCB, ACSL4, FANCE, FANCD2, FANCC, FANCA, EYA1, ERCC4, ERCC3, ERCC1, EP300, ELN, EIF2S3, PHC1, ECHS1, DPAGT1, DNMT1, DYNC1I2, DLAT, DGUOK, TIMM8A, DDX3X, DDC, DCTN1, DARS1, CYP27A1, CTNNA2, CSF1R, NDUFA9, NDUFS1, ADGRG1, SPTBN2, CLRN1, USH2A, UCHL1, UBE3A, TULP1, TUB, TLR4, TAF13, TAF2, VAMP1, SURF1, ABCC8, ELOVL4, STAT4, SPTAN1, ATXN1, SPR, SPG7, SPAST, SOD1, SNCA, SLC20A2, SLC18A2, SLC16A2, SLC2A1, SLC1A4, STIL, SDHD, SDHA, SCN8A, VCP, VLDLR, BEST1, VRK1, ABCB7, LRAT, AP4M1, SLC6A5, AIFM1, PRPF3, PRPF4, BAZ1B, CACNA1G, AP1S2, SQSTM1, PROM1, PEX11B, GPAA1, CTSF, SLC25A12, PRKRA, CASK, CNTNAP1, PEX3, OFD1, PLA2G6, KLRC4, KDM5C, GAN, IFT88, AAAS, XRCC2, CLIP2, ATXN8OS, SAG, NDUFS2, PAX1, PEX14, PEX13, PEX12, PEX10, PEX6, PEX1, PDYN, PDHA1, PDGFRB, PDE6B, PDGFB, PDE6G, PDE6A, CHMP1A, PRKN, RTN2, PAH, OPA1, NTRK2, NRL, NRAS, NEU1, NEK2, NEK1, NEFH, NDUFV2, NDUFS8, NDUFS4, NDUFV1, NDUFS3, PIGA, PLG, PLP1, EXOSC9, RPE65, RPGR, RP2, RP1, RP9, ROM1, RLBP1, RHO, RGR, RFC2, PRPH2, RBP3, RARS1, RAD51C, RAD51, ALDH18A1, PEX5, PEX2, PEX19, PTS, PSEN1, PSAP, HTRA1, PRPH, PRNP, PRKCG, PPP3CA, PPP2R2B, PODXL, IL12A-AS1
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Neutrophilia
Wikipedia
External links [ edit ] Classification D DiseasesDB : 8995 External resources eMedicine : med/3209 v t e Diseases of monocytes and granulocytes Monocytes and macrophages ↑ -cytosis : Monocytosis Histiocytosis Chronic granulomatous disease ↓ -penia : Monocytopenia Granulocytes ↑ -cytosis : granulocytosis Neutrophilia Eosinophilia / Hypereosinophilic syndrome Basophilia Bandemia ↓ -penia : Granulocytopenia/agranulocytosis ( Neutropenia / Severe congenital neutropenia / Cyclic neutropenia Eosinopenia Basopenia ) Disorder of phagocytosis Chemotaxis and degranulation Leukocyte adhesion deficiency LAD1 LAD2 Chédiak–Higashi syndrome Neutrophil-specific granule deficiency Respiratory burst Chronic granulomatous disease Neutrophil immunodeficiency syndrome Myeloperoxidase deficiencyPTAFR, RAC2, CSF3, IL6, MVK, CXCL8, OTULIN, SLC35C1, IL17A, IL1B, CRP, IL1A, TNF, IL10, CXCR2, MMP9, IFNG, CSF2, ELANE, CXCL1, IL5, IL25, IL33, GSTM1, IL4, NFE2L2, IL13, CXCR4, BRD4, SLC27A5, ITGB2, CD274, JAK2, ABCA1, GPT, TLR4, PTGDR, CXCL5, ALB, TAC1, NLRP3, IL17F, TEK, PARP9, CEL, TLR2, MYDGF, ABL1, TGFB1, FEV, TYROBP, SPP1, TNFRSF1A, PPM1D, SLC6A2, CCL4L2, TCN1, TACR1, TP53, TLR3, TG, BECN1, DDX58, TRAF3IP2, CD177, CCL4L1, FFAR4, PGP, CLEC9A, COPD, CRTC2, CABS1, WDR26, MAP3K19, CRTC3, ROBO3, LTB4R2, CYSLTR1, SARS2, TLR9, IL23A, BPIFA1, TBX21, SIGLEC9, SETBP1, SELE, SMUG1, PADI4, CCL27, SFTPD, PREP, CXCL12, CCR1, GSTM2, CXCL2, NR3C1, GABPA, ESR1, EPHB1, ELK3, EGFR, CSF3R, COX8A, MAP3K8, COL1A1, CLCA1, HIF1A, CEBPB, CEACAM5, CD47, CALCA, BCHE, AR, FAS, APOA1, BIRC3, APC, AHR, ADA, GZMB, IL1R1, CCL11, PDE4A, CCL5, CCL4, SCNN1B, SARS1, RNASE3, PLAAT4, MAP2K3, MAPK3, CTSA, PPARG, PON2, SLC26A4, MYD88, IL1RN, MUC5AC, MPO, MMP8, MIF, MCAM, LTA4H, LGALS3, ITGAM, CXCL10, IL15, IL7, IL4R, MUC5B
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Reticular Erythematous Mucinosis
Wikipedia
Reticular erythematous mucinosis Other names Midline mucinosis , [1] Plaque-like cutaneous mucinosis , [2] and REM syndrome [2] Specialty Dermatology Reticular erythematous mucinosis (REM) is a skin condition caused by fibroblasts producing abnormally large amounts of mucopolysaccharides . ... External links [ edit ] Classification D ICD - 10 : L98.5 ( ILDS L98.540) v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum This cutaneous condition article is a stub .
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Enteric Duplication Cyst
Wikipedia
External links [ edit ] Gastrointestinal duplications at Medscape v t e Congenital malformations and deformations of digestive system Upper GI tract Tongue , mouth and pharynx Cleft lip and palate Van der Woude syndrome tongue Ankyloglossia Macroglossia Hypoglossia Esophagus EA/TEF Esophageal atresia: types A, B, C, and D Tracheoesophageal fistula: types B, C, D and E esophageal rings Esophageal web (upper) Schatzki ring (lower) Stomach Pyloric stenosis Hiatus hernia Lower GI tract Intestines Intestinal atresia Duodenal atresia Meckel's diverticulum Hirschsprung's disease Intestinal malrotation Dolichocolon Enteric duplication cyst Rectum / anal canal Imperforate anus Rectovestibular fistula Persistent cloaca Rectal atresia Accessory Pancreas Annular pancreas Accessory pancreas Johanson–Blizzard syndrome Pancreas divisum Bile duct Choledochal cysts Caroli disease Biliary atresia Liver Alagille syndrome Polycystic liver disease
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Autoimmune Disease, Multisystem, Infantile-Onset, 2
Omim
Clinical Features Chan et al. (2016) reported a brother and sister, born of unrelated Caucasian parents, with onset of a systemic autoimmune disorder in the first months of life. The boy developed nephrotic syndrome at age 9 months, and renal biopsy showed mild IgG deposition with widespread foot process effacement consistent with minimal change disease. ... His sister developed bullous pemphigoid at 1 month of age, followed by inflammatory colitis, proteinuria in the absence of nephrotic syndrome, and autoimmune hypothyroidism. ... INHERITANCE - Autosomal recessive ABDOMEN Gastrointestinal - Inflammatory colitis GENITOURINARY Kidneys - Nephrotic syndrome (1 patient) - IgG deposition (1 patient) - Effacement of podocytes (1 patient) - Minimal change disease (1 patient) - Proteinuria SKIN, NAILS, & HAIR Skin - Blistering skin disease - Bullous pemphigoid ENDOCRINE FEATURES - Autoimmune hypothyroidism (1 patient) HEMATOLOGY - Autoantibodies to factor VIII (1 boy) IMMUNOLOGY - Autoimmune disorder - Autoantibody production - Decreased numbers of CD8+ T cells - Diminished proliferative response of T cells MISCELLANEOUS - Onset in infancy - A brother and sister from 1 family have been reported (last curated June 2016) - Both patients had resolution of symptoms after hematopoietic stem cell transplantation MOLECULAR BASIS - Caused by mutation in the zeta-chain-associated protein kinase gene (ZAP70, 176947.0006 ) ▲ CloseZAP70, ADCY7, CPT1C, RMI2, C1QTNF6, ANKRD30A, KCNH7, NKD1, NEURL4, ARID5B, ANKRD55, CARD9, ERAP2, BACH2, PLEKHA1, ARHGAP31, ZMIZ1, ATG16L1, UBASH3A, LRRK2, IL23R, PTPN22, PUS10, LINC02341, LINC00993, PTCSC2, LINC00824, LINC01250, MIR3681HG, LINC00271, INS-IGF2, IRF1-AS1, C1orf141, LINC02649, C12orf42, LURAP1L, CCDC88B, CUTALP, SPATA13, MB21D2, IGF2-AS, TMEM131, ALDH2, CRB1, RAB5C, RAB5B, PTPN2, PSMD5, TNFRSF11B, NTRK1, SMAD3, LPP, JAK1, IRF5, IL2RA, GPR35, FUT2, FLT3, FAP, DAG1, CAMK4, SLC22A5, STAT4, SUOX, RASGRP1, ADGRL2, FNBP1, ATXN2L, CD226, VAV3, DLEU1, PLXNC1, SH2B3, TG, TNFSF15, ELMO1, SH2D2A, CCN4, UBE2L3, TYK2, TPO, LINC02357
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Fissure Of The Nipple
Wikipedia
External links [ edit ] Classification D ICD - 10 : N64.0 , O92.1 ICD - 9-CM : 611.2 v t e Breast disease Inflammation Mastitis Nonpuerperal mastitis Subareolar abscess Granulomatous mastitis Physiological changes and conditions Benign mammary dysplasia Duct ectasia of breast Chronic cystic mastitis Mammoplasia Gynecomastia Adipomastia (lipomastia, pseudogynecomastia) Breast hypertrophy Breast atrophy Micromastia Amastia Anisomastia Breast engorgement Nipple Nipple discharge Galactorrhea Inverted nipple Cracked nipples Nipple pigmentation Masses Galactocele Breast cyst Breast hematoma Breast lump Pseudoangiomatous stromal hyperplasia Other Pain Tension Ptosis Fat necrosis Amazia v t e Pathology of pregnancy , childbirth and the puerperium Pregnancy Pregnancy with abortive outcome Abortion Ectopic pregnancy Abdominal Cervical Interstitial Ovarian Heterotopic Embryo loss Fetal resorption Molar pregnancy Miscarriage Stillbirth Oedema , proteinuria and hypertensive disorders Gestational hypertension Pre-eclampsia HELLP syndrome Eclampsia Other, predominantly related to pregnancy Digestive system Acute fatty liver of pregnancy Gestational diabetes Hepatitis E Hyperemesis gravidarum Intrahepatic cholestasis of pregnancy Integumentary system / dermatoses of pregnancy Gestational pemphigoid Impetigo herpetiformis Intrahepatic cholestasis of pregnancy Linea nigra Prurigo gestationis Pruritic folliculitis of pregnancy Pruritic urticarial papules and plaques of pregnancy (PUPPP) Striae gravidarum Nervous system Chorea gravidarum Blood Gestational thrombocytopenia Pregnancy-induced hypercoagulability Maternal care related to the fetus and amniotic cavity amniotic fluid Oligohydramnios Polyhydramnios Braxton Hicks contractions chorion / amnion Amniotic band syndrome Chorioamnionitis Chorionic hematoma Monoamniotic twins Premature rupture of membranes Obstetrical bleeding Antepartum placenta Circumvallate placenta Monochorionic twins Placenta accreta Placenta praevia Placental abruption Twin-to-twin transfusion syndrome Labor Amniotic fluid embolism Cephalopelvic disproportion Dystocia Shoulder dystocia Fetal distress Locked twins Nuchal cord Obstetrical bleeding Postpartum Pain management during childbirth placenta Placenta accreta Preterm birth Postmature birth Umbilical cord prolapse Uterine inversion Uterine rupture Vasa praevia Puerperal Breastfeeding difficulties Low milk supply Cracked nipples Breast engorgement Childbirth-related posttraumatic stress disorder Diastasis symphysis pubis Postpartum bleeding Peripartum cardiomyopathy Postpartum depression Postpartum psychosis Postpartum thyroiditis Puerperal fever Puerperal mastitis Other Concomitant conditions Diabetes mellitus Systemic lupus erythematosus Thyroid disorders Maternal death Sexual activity during pregnancy Category This medical article is a stub .
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Nephronophthisis
Medlineplus
Nephronophthisis can occur as part of separate syndromes that affect other areas of the body; these are often referred to as nephronophthisis-associated ciliopathies. For example, Senior-Løken syndrome is characterized by the combination of nephronophthisis and a breakdown of the light-sensitive tissue at the back of the eye (retinal degeneration); Joubert syndrome affects many parts of the body, causing neurological problems and other features, which can include nephronophthisis.
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Nevus Sebaceous
Wikipedia
External links [ edit ] Classification D ICD-O : M8410/0, M8410/3 v t e Cancers of skin and associated structures Glands Sweat gland Eccrine Papillary eccrine adenoma Eccrine carcinoma Eccrine nevus Syringofibroadenoma Spiradenoma Apocrine Cylindroma Dermal cylindroma Syringocystadenoma papilliferum Papillary hidradenoma Hidrocystoma Apocrine gland carcinoma Apocrine nevus Eccrine / apocrine Syringoma Hidradenoma or Acrospiroma / Hidradenocarcinoma Ceruminous adenoma Sebaceous gland Nevus sebaceous Muir–Torre syndrome Sebaceous carcinoma Sebaceous adenoma Sebaceoma Sebaceous nevus syndrome Sebaceous hyperplasia Mantleoma Hair Pilomatricoma / Malignant pilomatricoma Trichoepithelioma Multiple familial trichoepithelioma Solitary trichoepithelioma Desmoplastic trichoepithelioma Generalized trichoepithelioma Trichodiscoma Trichoblastoma Fibrofolliculoma Trichilemmoma Trichilemmal carcinoma Proliferating trichilemmal cyst Giant solitary trichoepithelioma Trichoadenoma Trichofolliculoma Dilated pore Isthmicoma Fibrofolliculoma Perifollicular fibroma Birt–Hogg–Dubé syndrome Hamartoma Basaloid follicular hamartoma Folliculosebaceous cystic hamartoma Folliculosebaceous-apocrine hamartoma Nails Neoplasms of the nailbed This Epidermal nevi, neoplasms, cysts article is a stub .
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Ophthalmodynia Periodica
Wikipedia
Ophthalmodynia periodica Other names Needle-in-the-eye syndrome, sharp short-lived head pain, [1] jabs and jolts syndrome [2] Ophthalmodynia periodica is also known as " ice-pick headache ", is a primary headache disorder , so it is not caused by any other conditions. ... External links [ edit ] WebMd article on Ice Pick Headaches Healthline article on Ice Pick Headaches Primary Stabbing Headaches Classification D ICD - 10 : G44.800 v t e Headache Primary ICHD 1 Migraine Familial hemiplegic Retinal migraine ICHD 2 Tension Mixed tension migraine ICHD 3 Cluster Chronic paroxysmal hemicrania SUNCT ICHD 4 Hemicrania continua Thunderclap headache Sexual headache New daily persistent headache Hypnic headache Secondary ICHD 5 Migralepsy ICHD 7 Ictal headache Post-dural-puncture headache ICHD 8 Hangover Medication overuse headache ICHD 13 Trigeminal neuralgia Occipital neuralgia External compression headache Cold-stimulus headache Optic neuritis Postherpetic neuralgia Tolosa–Hunt syndrome Other Vascular