Disease

Systemic Lupus Erythematosus

About the Disease
Systemic Lupus Erythematosus, also known as lupus nephritis, is related to lupus erythematosus and autoimmune disease, and has symptoms including exanthema, pruritus and lupus-like rash. An important gene associated with Systemic Lupus Erythematosus is TREX1 (Three Prime Repair Exonuclease 1), and among its related pathways/superpathways are Innate Immune System and NF-kappaB Signaling. The drugs Sulfamethoxazole and Trimethoprim have been mentioned in the context of this disorder. Affiliated tissues include Umbilical Cord, bone marrow and skin, and related phenotypes are lupus nephritis and arthritis

Common Targets
CD226 | HSP90B1 | CALU | TPST2 | ERC2 | MIR1279 | CD1C | LOC105379395 | HLA-DQB1-AS1 | PIM2 | ATF6B | CALM2 | IL23R | TNFSF4 | GRB2 | MIR505 | IL18 | G7422 | MYO5C | CD40LG | CGAS | ASGR1 | ADAM10 | CD19 | HLA-C | Asialoglycoprotein Receptor (ASGPR) (nonspecified subtype) | KIR3DL2 | KLRC1 | DNASE1 | YDJC | FCN2 | OAS1 | PNPT1 | PER2 | TLR7 | WFDC8 | PTPN6 | TNFRSF9 | ITGAM | KIR3DS1 | KAZN | G238 | PIK3CG | TNFRSF6B | G114548 | Protein Phosphatase 2B | IRAK2 | CXCR5 | JAK3 | MYNN | TEC | FCGR2B | PIK3R5 | PPIA | CD36 | Interferon-alpha (IFN-alpha) (nonspecified subtype) | PVT1 | JAK1 | SOS1 | CCR10 | TLR5 | MPO | TNFRSF11B | IL22 | MIR210HG | PRPS2 | HLA-DQB1 | XRCC1 | PDE4D | CYSTM1 | PLD1 | ICOS | ID1 | Glucosidase (nonspecified subtype) | SPP1 | IL33 | G596 | LCE3B | TRIM22 | CSMD3 | G6714 | CD74 | GPBAR1 | DNASE1L3 | MEGF11 | KDR | CRBN | CD247 | TNFSF8 | RORC | MFGE8 | TRIM25 | TNFRSF25 | PADI2 | ECT2 | PTPN2 | SAMD9 | PXK | LCE3C | FLJ42969 | GAPDH | USP35 | CDK4/Cyclin D1 | CFB | CDH13 | GPR35 | TRAF2 | PADI4 | MAD1L1 | GSR | IFNB1 | IL-15 receptor | SP100 | MAN2B2 | CAMK4 | VSTM2B-DT | GFPT2 | TLR8 | PLD2 | MALT1 | LYST | G1956 | CIITA | IL23A | TIMD4 | G3845 | LOC728392 | ABL1 | RBFOX1 | PADI1 | ANXA3 | Interleukin 17 (nonspecified subtype) | TNPO3 | IFNA13 | TLR3 | C1S | ATP1B4 | PDK1 | TRIM15 | AMBRA1 | GTF2I | HLA-F | PHRF1 | IL12B | JAK2 | EVA1A | CD6 | LOC105370819 | IL1B | TNFRSF1B | KCNA3 | SFTA2 | G1026 | MAP2K7 | CPSF6 | MDK | FEN1 | GJB3 | HMGXB4 | HLA-DMB | TLR8-AS1 | DEF6 | SLFN12 | GSS | RIPOR2 | DHRS12 | WEE2-AS1 | MKNK2 | RNASEH2A | GREB1 | RABGAP1L | PHF11 | LRRK2 | SLC22A1 | GRIN1 | RSAD2 | UBE4A | PSMB9 | Tyrosine-Protein Kinases Src (nonspecified subtype) | JMJD7 | GLIS3 | LUM | ACSF3 | PTCHD1-AS | SLC7A7 | CMPK2 | G6774 | GHSR | Interleukin 21 receptor complex | IL1RN | Interleukin-1 (nonspecified subtype) | CALM3 | HCP5 | KRT1 | KIAA0319L | TNFSF13 | HDAC8 | LINC00299 | CSK | NOS1 | LTO1 | NFKB2 | MORC2 | IFNL3 | M6PR | PDE4B | MIR3202-2 | CHST12 | HPD | IKBKB | MIR1-1HG | SNRPB | G7015 | OAS2 | ADARB2 | PHTF1 | IFI44L | ADD2 | G3569 | SCLT1 | ZFP36L1 | TPMT | FCGRT | ANKS1A | PARP9 | HDAC6 | PRKCG | CTPS1 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | NDUFS4 | CLEC4A | LINC01281 | RARA | LY6E | DDX60L | IRF2 | CFD | FZD3 | G59272 | KLB | TMPRSS4 | FCHSD2 | AGRN | SNRPD1 | OAS3 | HERC5 | DHRS9 | CD101-AS1 | IL19 | IGHE | KCND3 | DNMT3A | BTK | VKORC1 | ADCY3 | Heat shock protein 90 (nonspecified subtype) | RASGRP3 | C5 | DGUOK-AS1 | XAF1 | HLA-DQB2 | CNR2 | CTSS | PCNX3 | ERC1 | IL17RA | LOC101927960 | LGALS3BP | MICALL1 | IFI27 | ELANE | IFIT5 | G595 | PRKCA | IL3 | ACTE1P | CALM1 | IRAK3 | Folate Receptor (nonspecified subtype) | ANKRD36 | TAF4 | APLNR | FKBP1A | CARD11 | TMOD2 | IRF3 | HDAC7 | CSTA | NPM1 | TNIK | IL2RA | G6352 | LTA | ZNF804B | PAX3 | SPPL2A | CCR4 | Matrix Metalloproteinase (MMP) (nonspecified subtype) | TGFB1 | NRAS | NR1H3 | EIF2AK2 | MECP2 | GEMIN4 | CDK6 | CHEK1 | BAK1 | ERG | MSH5 | NCF2 | TRIM56 | PPP3R2 | HLA-DQA1 | NID1 | RNF220 | IQGAP2 | LCK | MORC4 | ATP5IF1 | MC2R | PLSCR1 | EED | ATG5 | BMX | ABCG1 | SRI | CCDC88C | TSBP1-AS1 | Lipoxygenase (nonspecified subtype) | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | ENTREP2 | PAK5 | MAP3K8 | Protein kinase C (nonspecified subtype) | LYG2 | BACE2 | BRD2 | XXYLT1 | NF-kappaB (NFkB) | G7099 | TYK2 | FBN2 | IL1RL1 | HLA-DOB | ATP10A | TRAF6 | PIM3 | F3 | PPP3CC | LOC105377923 | TNFSF13B | HLA-G | APOH | BMP8A | MKNK1 | S1PR4 | S1PR2 | HSPE1 | mTOR complex 1 | IL4R | IL7R | CSF1R | PGPEP1L | BMP1 | UBE2L3 | ALPK1 | TNFSF10 | ZCCHC2 | G5133 | ATP6V1B1 | PARVG | EGR2 | ATG16L1 | ADAM17 | KEAP1 | HSF1 | PLD4 | DHODH | PSD3 | MAP3K14 | IL3RA | KCNN4 | CDK11A | TNFSF11 | CD14 | CD48 | SLC9A3 | CD3 Complex (T Cell Receptor Complex) | ESR2 | G4780 | MIDEAS | BTNL2 | PARP11 | HMGCR | TRANK1 | B4GALNT4 | LEP | IKZF1 | CD86 | TIRAP | PHLDB1 | NOTCH4 | CAST | PIK3CB | CDK4 | KIR2DL5B | HLA-B | MICB | CCDC113 | HLA-DQA2 | AKAP2 | IFITM1 | FAM200B | G29126 | FBLN7 | KIT | C1QC | NUDT1 | SCAMP2 | HIP1 | IL-2 receptor | ARG1 | DLEU1 | SLC15A4 | LDLRAP1 | MAPT-AS1 | RNF213 | ICAM1 | G7852 | PBX3 | LILRA4 | BCR | IL-20 receptor | CCDC136 | LGALS9 | TRAP1 | XKR6 | LOC105378019 | USP18 | CNR1 | CLEC4C | G6772 | ABCA1 | NAA10 | PECAM1 | IL32 | GRM7 | CELSR1 | XIAP | S100A5 | ARID5B | MEF2D | SLC44A4 | LOC105371388 | FCRL3 | G4137 | ITGA11 | TMEM187 | CPNE3 | HLA-DRB1 | CCN2 | BRD4 | WAKMAR2 | PIK3CD | EIF2AK4 | AIMP2 | ZNF875 | GIMAP8 | ADA | IL15 | S1PR3 | CCR2 | MIR21 | IL12RB2 | SELP | IL27 | SMURF1 | NCK1 | FLI1 | SYNGR1 | HLA-DPA1 | EVL | FOXN3 | ZAP70 | UBASH3A | SIGLEC14 | AP4B1-AS1 | MIR181A2HG | JAKMIP3 | SLC12A7 | PPARD | HSD11B1 | HSPA8 | PRSS54 | CD38 | XPO1 | IRAK4 | MPIG6B | R3HCC1L | CLDN10 | CD40 | CYP24A1 | ULK3 | CD22 | HLA-DRA | Interleukin-12 (IL-12) | PLXDC2 | ACOT8 | Pim Kinase (nonspecified subtype) | CDK6/Cyclin D1 | ITK | DPP4 | ICAM5 | FKBP5 | R3HDM1 | COPA | AKR1B1 | LAMC2 | NBDY | OR51E1 | SMYD3 | SYK | C1QA | TRPV1 | G581 | ADORA2A | STK32C | TET2 | MAP4K1 | LSP1 | MX1 | RTKN2 | PTPRM | STIM1 | DOCK1 | EPC1 | PRKCD | LOC105371664 | G3605 | KLK1 | MMP7 | PTPN5 | PRF1 | CSMD1 | HIPK4 | XDH | KLF2 | F2 | TASL | PRKD3 | RPS24 | IL15RA | G4170 | CROCC2 | HDAC1 | PTGS1 | RPP14 | PTPN1 | PSORS1C1 | FCGR3A | NMNAT2 | Immunoproteasome | PADI3 | HAVCR1 | C4A | SERPINE1 | GLRX2 | SHOC2 | PPARG | GPIHBP1 | RFX1 | SATB1 | BICD1 | SYNDIG1L | P2RY12 | JAZF1 | GPR19 | DDX60 | IFI44 | BIRC3 | PELI2 | TRIM31 | CYP2R1 | IL5 | ST8SIA4 | G920 | IFIT1 | MBL2 | CD82 | LOC102725019 | G9734 | Interferon (nonspecified subtype) | PSORS1C2 | CACNA1D | NADSYN1 | PELI1 | Polycomb Repressive Complex 2 | ICOSLG | GPR84 | DNAH17 | IRF5 | GPR183 | NLRC5 | LOC285626 | SLAMF1 | LST1 | LRRC8A | LRP1 | PNP | ERI3 | NRXN1 | LOC105376397 | HLA-A | KIR2DL5A | S100A9 | CXCL12 | LINC01845 | NUAK1 | DAPK1 | ELF1 | TNFAIP3 | GSTT1 | TLR2 | PLCG1 | MS4A1 | CCL17 | MALAT1 | DDO | OGA | LRRC18 | G2475 | LOC101928354 | GTF2IRD1 | PIK3R6 | MCM2 | G3480 | G3630 | GABRR2 | CXCL13 | C1QB | JADE1 | GNRHR | LIME1 | IL17F | KIR2DL1 | CCND3 | HDAC4 | RAB31 | C1QTNF4 | IKZF3 | TRIM21 | COL19A1 | ASB18 | NAA25 | SAMHD1 | TET2-AS1 | EPSTI1 | COG6 | MMP13 | SMPD3 | GRM3 | LPIN2 | ZBTB20 | PARP14 | ST3GAL1 | LEPR | STAT4 | G2099 | GGT1 | FAR2 | MAN1A1 | ARHGAP26 | TLL1 | KDM1A | CD80 | ITPA | SPI1 | AGA | LANCL2 | HLA-DRB3 | KRTAP10-2 | FBXO31 | RAD51 | CLEC16A | S1PR5 | TNFRSF13C | RUNDC1 | MEFV | FPR2 | G836 | CD3E | IFIH1 | GASK1A | C1orf21 | BTLA | DOT1L | MAP4K3 | CDH3 | OASL | ISG15 | IFNW1 | OPN1SW | SSB | MIR29A | SPRED2 | FASN | G4318 | TRIM34 | AHI1-DT | CDYL | B2M | IFNAR1 | NQO2 | ERAP1 | PIN1 | IL1RL2 | GMPS | TNFRSF17 | EPHA2 | TLCD3B | BLTP3A | TNK2 | NOL4L | KIR2DL2 | Poly [ADP-ribose] polymerase (nonspecified subtype) | IL12A-AS1 | LOC101929755 | NR3C1 | AP-1 Transcription Factor Complex | BLK | SIK2 | LINC00578 | PRKCB | KIR3DL3 | High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7 (nonspecified protein) | ITPK1 | SRRM2 | LMOD1 | GPR173 | LINC02273 | CTTNBP2NL | Janus Kinase (nonspecified subtype) | GP6 | SPATS2L | CDHR5 | CDKN1B | KIR2DP1 | ZNFX1 | HLA-DRB4 | IL1A | IL12A | RNF126P1 | KCNS3 | G196 | TLL2 | G7157 | PTPN22 | LINC01777 | IFITM3 | CCL21 | IRF7 | NOS3 | GC | CDK8 | LOC105374793 | HTT | IRF8 | Inosine 5'-monophosphate dehydrogenase (IMPDH) (nonspecified subtype) | TNXB | PIM1 | PON1 | SPINK2 | IKZF2 | UNC80 | HSPA1B | TMEM123 | IFIT3 | RPN1 | MYB | FCGR2A | LINC01490 | PSMB8 | TSIX | SYT13 | SLC6A4 | SYT1 | IFNL4 | BISPR | FNDC3A | EPB41L3 | PDE4A | LOC105376626 | IL2 | FASLG | C5AR1 | OTUB1 | ARHGAP31 | IL21 | Complement Complex | LRRC63 | PPP3CB | SCAMP5 | TIMP2 | TNFRSF4 | HRH1 | LINC00367 | FCGR2C | ANXA1 | CXCR2 | CSGALNACT1 | Integrin alpha1beta1 (VLA-1) receptor | LAP3 | HSD17B1 | TIGIT | PPP3R1 | PRKCQ | HLA-DPB1 | CMKLR1 | LYN | MIR29B1 | IL20 | PDE5A | KIR2DL3 | AGTR2 | ODF3B | SMIM29 | NEMP2-DT | CDK6/Cyclin D3 | GLT1D1 | TAP1 | DNM3 | RIBC2 | ITPKB | C3 | IL1R2 | CD79B | TREX1 | KLHDC7B | KIR2DS2 | SH2B3 | PNPLA1 | MAP2K2 | HCFC1 | LANCL3 | LHFPL3 | KIR2DL4 | AGTR1 | MMP2 | ANKRD13C | TNIP1 | CCL24 | FLII | HMSD | CFH | G3146 | SLC11A1 | AGER | NAMPT | KIRREL1 | ZFP90 | Tubulin | MIR146A | TNFRSF8 | APOB | PLCH1 | LRP1B | POLB | HCG20 | ANKRD45 | FAS | TLR9 | LOC101928512 | HLA-DRB5 | G5743 | WDFY4 | cGMP-inhibited 3',5'-cyclic phosphodiesterase 3 (PDE3) (nonspecified subtype) | KIR2DS1 | VDR | Ras GTPase (nonspecified subtype) | ARHGAP4 | MIR29B2 | FCGR3B | NOS2 | TSBP1 | POLR3A | FSTL1 | PXT1 | GATA3 | BST2 | CABP1 | IFNG | IRAK1 | KIR2DS3 | HLA-DPB2 | KRR1 | EEA1 | LRRC49 | FCER1A | NPLOC4 | TBC1D23 | GPSM3 | Immunoglobulin A | METTL15 | LINC02571 | CD28 | LOC107986092 | RAP1GAP | DMD | SERPING1 | HELZ2 | WDR20 | TBK1 | TRAF3IP2 | SOGA1 | CTLA4 | SH2D1A | IDS | Innate Repair Receptor (IRR) | MIF | UBN2 | PIK3CA | ATG16L2 | ABCC4 | STUM | DGKG | G2064 | GALC | TMEM161B-DT | IRF9 | AFG3L2 | STING1 | CCR5 | GIMAP5 | VSIR | CYP27B1 | LGALS1 | ZPBP2 | TRIM40 | RIPK1 | IKBKE | TNFRSF13B | PTPN11 | HRH4 | S1PR1 | DPH5 | GSTM1 | SIGLEC6 | SLC8A1 | KIR2DS4 | Peptidyl arginine deiminase (PAD) (nonspecified subtype) | TXK | PTPRC | Interleukin-7 receptor | TAP2 | NLRP3 Inflammasome | ATXN2 | SIK3 | CAMKK2 | OR2B11 | DHFR | G7124 | WDR25 | PDE7A | MICA | CCDC149 | KIR2DS5 | MATN2 | NR2F6 | PDGFRA | MIR6882 | SHKBP1 | IL6R | SLC6A3 | MTHFR | CD5 | Interleukin 23 complex (IL-23) | HLA-V | IL10 | VHL | FLT3 | LOC105379185 | CNTNAP4 | AP5B1 | IFNAR2 | IL4 | RHOA | LGALS12 | BANK1 | ICA1 | KIR3DL1 | IL21R | LOC100506023 | Proteasome Complex | S100G | CR2 | LY6E-DT | MIR1307 | PPT1 | ADAR | ZNF827 | NCF1 | ETS1 | C2 | CADPS | ZRANB2-DT | GRIN2B | MCCD1 | SMARCAL1 | RIGI | AHI1 | GPR55 | PARP10

疾病靶点研报
Systemic Lupus Erythematosus

Note: If you'd like to get a target analysis report for Systemic Lupus Erythematosus, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Systemic Lupus Erythematosus at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Motion Sickness | Rhabdomyosarcoma, Alveolar | Congenital Absence Of Vas Deferens | Glutaric Aciduria Type 2 | Headache | Actinomycetoma | Maternally Inherited Diabetes And Deafness | Branchiootorenal Syndrome | Klinefelter Syndrome | Fibrosis | Prolactinoma | Pendred Syndrome | Polydactyly | Dermatofibrosarcoma | Multifocal Motor Neuropathy | Sleep Apnea | Spondylometaphyseal Dysplasia | Meningioma, Benign | Cholelithiasis | Chondrosarcoma | Familial Advanced Sleep Phase Syndrome | Stroke | Chorea-acanthocytosis | Behavioral Variant Of Frontotemporal Dementia | Hyperparathyroidism, Primary | Liddle Syndrome | Diabetes Type 1 | Auriculocondylar Syndrome | Muckle-Wells Syndrome | Ichthyosis | Waardenburg Syndrome Type 1 | Tularemia | Hepatic Adenomatosis | Polyomavirus Nephropathy | Necrotizing Autoimmune Myopathy | Antisocial Personality Disorder | Fanconi Syndrome | Metatropic Dysplasia | Vertigo | Mitochondrial Disease | Malaria | Mucolipidosis Type IV | Pineoblastoma | HELLP Syndrome | Primary Ovarian Insufficiency | Albinism | Neurocysticercosis | Basal Cell Nevus Syndrome | Van Der Knaap Disease | Pelvic Inflammatory Disease | Meningeal Melanocytoma | Ameloblastoma | Endocarditis | Swine Influenza | Spondyloperipheral Dysplasia | Renal-hepatic-pancreatic Dysplasia | Pulmonary Vein Stenosis | Osteogenesis Imperfecta Type I | Esotropia | Hemochromatosis Type 1 | Pituitary Disorders | Short-chain Acyl-CoA Dehydrogenase Deficiency | Argininosuccinic Aciduria | Transthyretin-related Amyloidosis | Thrombocythemia, Essential | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Trismus-pseudocamptodactyly Syndrome | Multiple System Atrophy | Cherubism | Primary Progressive Aphasia | Chronic Lymphocytic Leukemia | Spinocerebellar Ataxia Type 20 | Dwarfism | Cerebral Cavernous Malformations | Impulse Control Disorder | Tendinopathy | Hashimoto Thyroiditis | Leukodystrophies | Sarcoma, Ewing | Oculocutaneous Albinism Type 2 | Congenital Hemolytic Anemia | Myelitis, Transverse | Spinocerebellar Ataxia Type 38 | Calcium Pyrophosphate Deposition Disease | Inflammatory Joint Disease | Kaposi Sarcoma | Autosomal Recessive Congenital Ichthyosis | Leukemia-lymphoma, Adult T-cell | Pierson Syndrome | Papillorenal Syndrome | Trimethylaminuria | Porphyria, Variegate | Adenocarcinoma | Urea Cycle Disorder | Chediak-Higashi Syndrome | Paget's Disease Of The Breast | Herpes Genitalis | Corneal Ulcer | Castleman Disease | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Paraganglioma | B-cell Prolymphocytic Leukemia | Hypercalcemia | Keratosis | Macrodactyly | Neurofibromatosis-Noonan Syndrome | Rotor Syndrome | Syndactyly | Infantile Neuroaxonal Dystrophy | Cerebrotendinous Xanthomatosis | Hydrolethalus Syndrome | Autism | Spinal Cord Diseases | Huntington's Disease-like 2 | Pleurisy | Heart Block | Analgesia | Lesch-Nyhan Syndrome | Fibronectin Glomerulopathy | Metachromatic Leukodystrophy | DiGeorge Syndrome | Osteosarcoma | Trichotillomania | Diabetes | Hereditary Coproporphyria | Hypolipoproteinemia | Cyclic Vomiting Syndrome | Cardiac Sarcoidosis | Spinocerebellar Ataxia Type 14 | Spinal Muscular Atrophy | Chronic Myeloid Leukemia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Myasthenia Gravis | Primary Lateral Sclerosis | Leiomyoma | Inborn Errors Of Metabolism | Congenital Bilateral Absence Of Vas Deferens | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Retinitis | Panniculitis | Fragile X Syndrome | Citrullinemia | FG Syndrome | Progressive External Ophthalmoplegia | Pneumonia, Viral | Facioscapulohumeral Muscular Dystrophy | Saethre-Chotzen Syndrome | Prolidase Deficiency | Restrictive Dermopathy | Hypocalcemia | Osteitis | Spinocerebellar Ataxia Type 7 | Sezary Syndrome | Familial Hyperaldosteronism | Nevus | Hepatitis, Autoimmune | Usher Syndrome Type I | Low Tension Glaucoma | C3 Glomerulonephritis | Gastrointestinal Disorders | Multiple Sclerosis, Chronic Progressive | Cockayne Syndrome | Granular Corneal Dystrophy Type 1 | Neurodegeneration With Brain Iron Accumulation | Allan-Herndon-Dudley Syndrome | Insulinoma | Hyperthermia, Malignant | Pyruvate Decarboxylase Deficiency | Osteogenesis Imperfecta Type V | Glomerulonephritis, Membranoproliferative | Cancer, Kidney | CDKL5 Deficiency Disorder | Thrombophilia | Acute Tubular Necrosis | GLUT1 Deficiency Syndrome | Gastroenteritis, Eosinophilic | Vertebrobasilar Insufficiency | Metabolic Diseases | Lymphedema | Frank-ter Haar Syndrome | Hartnup Disease | Hypertrophy | Familial Cerebral Amyloid Angiopathy | Ectodermal Dysplasia | Blepharitis | Anencephaly | Keratopathy | Encephalocele | Primary Hyperoxaluria Type 1 | Spinocerebellar Ataxia Type 10 | Spinal Muscular Atrophy Type 2 | Giant Cell Glioblastoma | Pericarditis | Sporadic Inclusion Body Myositis | Greig Cephalopolysyndactyly Syndrome | Crisponi Syndrome | Hypopituitarism | Renal Hypomagnesemia 3 | Uremic Pruritus | Waardenburg Syndrome Type 2E | Scapuloperoneal Spinal Muscular Atrophy | Vascular Cognitive Impairment | Neuromyelitis Optica | N-acetylglutamate Synthase Deficiency | Chorioretinitis | LEOPARD Syndrome | Scleroderma | Amyotrophic Lateral Sclerosis, Juvenile | Carcinoma In Situ | Hyperparathyroidism-jaw Tumor Syndrome | Reflex Epilepsy | Long QT Syndrome Type 1 | Chromosome 9q34.3 Deletion Syndrome | Spinocerebellar Ataxia Type 5 | Vitreoretinal Degeneration, Snowflake Type | Subcortical Band Heterotopia | Schnitzler Syndrome | Dysgerminoma | Leukemia | Shwachman-Bodian-Diamond Syndrome | Primary Progressive Nonfluent Aphasia | Hypervalinemia | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Dementia | Wolfram Syndrome 2 | Partington Syndrome | Angioimmunoblastic T-cell Lymphoma | Hepatic Veno-occlusive Disease | Arthritis, Reactive | Diabetes Mellitus, Transient Neonatal | Alzheimer Disease, Late Onset | Lichen Sclerosus | Hepatitis A | Carbohydrate Metabolism Disorders | Iron Metabolism Disorders | Gastroenteritis | Onchocerciasis | Blomstrand Osteochondrodysplasia | Duodenal Atresia | Cardiomyopathy, Hypertrophic | Charcot-Marie-Tooth Disease, Type 2C | Cyst | Angiodysplasia | Neurofibromatosis Type 2 | Dubin-Johnson Syndrome | Megalencephaly | Anxiety Disorders | Combined Malonic And Methylmalonic Acidemia | Galloway-Mowat Syndrome | Vitamin B12 Deficiency | Myositis, Focal | Epidermolysis Bullosa Dystrophica | Hypothalamic Obesity | Neural Tube Defect | Angina Pectoris | Hepatopulmonary Syndrome | Tumoral Calcinosis | Primary Erythromelalgia | Cystitis | Amelanotic Melanoma | Craniopharyngioma | Carcinoid Syndrome | Papillon-Lefevre Syndrome | Asphyxia Neonatorum | Adenoma, Pleomorphic | Hypercalciuria | Lateral Meningocele Syndrome | Coenzyme Q10 Deficiency | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Peeling Skin Syndrome, Acral Type | Traboulsi Syndrome | Robinow Syndrome | Seasonal Mood Disorder | Distal Myopathy | T-cell Lymphoma, Subcutaneous Panniculitis-like | Bethlem Myopathy | Endometrial Hyperplasia | Sarcoma, Endometrial Stromal | Budd-Chiari Syndrome | Liver Failure | Periodic Limb Movement Disorder | Cataplexy | Gastric Atrophy | Myotonic Disorders | Alkaptonuria | Pancytopenia | Lipid Storage Diseases | Enlarged Vestibular Aqueduct | DOCK8 Immunodeficiency Syndrome | Hereditary Spherocytosis | Strabismus | Mast Cell Leukemia | Centronuclear Myopathy | Leishmaniasis, Cutaneous | Pseudo-pseudohypoparathyroidism | Hyperferritinemia-cataract Syndrome | Achondrogenesis | Microcephalic Primordial Dwarfism | Fabry's Disease | Usher Syndrome Type II | Methemoglobinemia | Subacute Sclerosing Panencephalitis | Juvenile Polyposis | Marinesco-Sjogren Syndrome | Gardner Syndrome | Aplastic Anemia | Best Macular Dystrophy | Otosclerosis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Vestibular Disease | Hydrocephalus, Normal Pressure | Erythematotelangiectatic Rosacea | Ellis-Van Creveld Syndrome | Peripheral T-cell Lymphoma | Leri-Weill Dyschondrosteosis | Bietti Crystalline Dystrophy | Alpha-1 Antitrypsin Deficiency | Panic Disorder | Bullous Pemphigoid | Parvovirus B19 Infection | Dengue Hemorrhagic Fever | Glaucoma, Congenital | Hemolytic Anemia | Split Hand-foot Malformation | Acrocallosal Syndrome | Leishmaniasis, Visceral | Familial Hemiplegic Migraine | Pouchitis | Pseudohypoparathyroidism Type 1C | Porphyria Cutanea Tarda | Twin-to-twin Transfusion Syndrome | Infectious Diarrhea | Muscle Wasting | Colorectal Adenoma | Asperger Syndrome | Japanese Encephalitis | Hypotension, Orthostatic | Patent Ductus Arteriosus | Aarskog-Scott Syndrome | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Disseminated Superficial Actinic Porokeratosis | Cystinuria | Leukocyte Adhesion Deficiency Type 1 | Charcot-Marie-Tooth Disease Type 2T | Basal Ganglia Cerebrovascular Disease | Olmsted Syndrome | Epidermolytic Hyperkeratosis | Persistent Fetal Circulation | Gaucher Disease | Vogt-Koyanagi-Harada Syndrome | Adenylosuccinate Lyase Deficiency | Corneal Dystrophy And Perceptive Deafness | Kallmann Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Lymphoma Lymphoblastic | Dermatomyositis | Lung Diseases | Sarcosinemia | Incontinentia Pigmenti | Multisystemic Smooth Muscle Dysfunction Syndrome | Fontaine Progeroid Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Anal Fissure | Keratitis | Influenza | Uveitis, Anterior | Asthma, Exercise-induced | Aldosterone Synthase Deficiency | Fetal And Neonatal Alloimmune Thrombocytopenia | Aspergillosis | Pearson Syndrome | Non-epidermolytic Palmoplantar Keratoderma | ADNP Syndrome | Stargardt Disease | Sertoli Cell-only Syndrome | Borderline Personality Disorder | Hemochromatosis Type 2 | Polymyositis | Methylmalonic Aciduria And Homocystinuria, CblC Type | Poirier-Bienvenu Neurodevelopmental Syndrome | Coma | Systemic Lupus Erythematosus | Colitis, Collagenous | Aplasia Cutis Congenita | Monilethrix | Aldosteronism | Multicentric Carpotarsal Osteolysis Syndrome | Prostatitis | Hyperacusis | Eiken Syndrome | Myhre Syndrome | KBG Syndrome | Episodic Ataxia Type 2 | Arthrogryposis | Okihiro Syndrome | Connective Tissue Disorders | Congenital Torticollis | Familial Dysautonomia | Retinal Vasculitis | Narcolepsy