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

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

Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Carney-Stratakis Syndrome | Hypersensitivity Pneumonitis | Chudley-McCullough Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Ataxia-ocular Apraxia 2 | Esophageal Adenocarcinoma | Schizophrenia, Paranoid | Tricho-hepato-enteric Syndrome | Corneal Dystrophy | Parkinson Disease 6, Autosomal Recessive Early-onset | Nephrosclerosis | Haim-Munk Syndrome | Pseudohypoparathyroidism Type 1B | Meconium Ileus | Metachromatic Leukodystrophy | Basal Cell Nevus Syndrome | Primary Ovarian Insufficiency | Chromosome 8q21.11 Deletion Syndrome | Hyperparathyroidism | Osteogenesis Imperfecta Type II | Ameloblastoma | Pseudohypoparathyroidism Type 2 | Thyroid Dyshormonogenesis | Kashin-Beck Disease | Myopia | Hyperkeratosis | Acute Chest Syndrome | Hypoproteinemia, Hypercatabolic | Diabetic Encephalopathy | Bacterial Meningitis | Spinocerebellar Ataxia Type 16 | Myocarditis | Porphyria | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | DICER1 Syndrome | Esophagitis | Astrocytoma, Anaplastic | Papillorenal Syndrome | Extramammary Paget's Disease | Oculodentodigital Dysplasia | Paracoccidioidomycosis | Meningitis | Blue Nevus | Cholestasis, Intrahepatic | Disseminated Intravascular Coagulation | Reflex Epilepsy | Autism Spectrum Disorders | Dysferlinopathy | Carbonic Anhydrase VA Deficiency | Primary Torsion Dystonia | Tatton-Brown-Rahman Syndrome | Neuroblastoma | Scleroderma, Diffuse | Usher Syndrome Type II | Familial Advanced Sleep Phase Syndrome | Polyradiculopathy | Schistosomiasis Mansoni | Leukoencephalopathy, Progressive Multifocal | Pouchitis | Branchiootorenal Syndrome | Congenital Afibrinogenemia | Niemann-Pick Disease, Type C | Bruck Syndrome | Donnai-Barrow Syndrome | Congenital Bile Acid Synthesis Defect | Discoid Lupus Erythematosus | Castleman Disease | Schnitzler Syndrome | Hyperinsulinemic Hypoglycemia | Ischemia | Alopecia Areata | Pyloric Stenosis, Infantile Hypertrophic | Dermatofibrosarcoma | Imerslund-Grasbeck Syndrome | Hydrocephalus, Normal Pressure | Angiosarcoma Of The Breast | Meningococcal Infections | Amelanotic Melanoma | Thyrotoxic Periodic Paralysis | Purpura | Epithelial-myoepithelial Carcinoma | Split Hand-foot Malformation | Rash | Charcot-Marie-Tooth Disease Type 4B1 | Acquired Partial Lipodystrophy | Takotsubo Cardiomyopathy | Feingold Syndrome | Larsen Syndrome | Early Infantile Epileptic Encephalopathy 13 | Congenital Nystagmus | Acute Anterior Uveitis | Mitochondrial DNA Depletion Syndrome | Common Cold | Granuloma Annulare | Tonsillitis | T-cell Leukemia | Carbamoyl Phosphate Synthetase I Deficiency | Optic Nerve Hypoplasia, Bilateral | Frontometaphyseal Dysplasia | Stroke | Hyperandrogenemia | Cysticercosis | Corticobasal Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Liebenberg Syndrome | Hereditary Spastic Paraplegia | Hepatitis C, Chronic | Pheochromocytoma | Intellectual Disability, Autosomal Dominant 5 | Spondyloepiphyseal Dysplasia Tarda, X-linked | Cerebral Cavernous Malformations | Inborn Errors Of Metabolism | Motor Neuron Diseases | Pineoblastoma | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Temporal Lobe Epilepsy | Neuroleptic Malignant Syndrome | Sclerosteosis | D-2-Hydroxyglutaric Aciduria | Niemann-Pick Disease | Omenn Syndrome | Bartsocas-Papas Syndrome | X-linked Charcot-Marie-Tooth Disease | Palsy, Cerebral | Acral Lentiginous Melanoma | Graft-versus-host Disease | Osteomalacia | Kawasaki Disease | Splenomegaly | Acne | Colitis, Microscopic | Fibrillation, Atrial | Chronic Mucocutaneous Candidiasis | Bursitis | 3-methylglutaconic Aciduria | Cystitis | Rolandic Epilepsy | Pure Autonomic Failure | Miyoshi Myopathy | Zimmermann-Laband Syndrome | Zollinger-Ellison Syndrome | Infantile Liver Failure Syndrome 1 | Tietze Syndrome | Heimler Syndrome | Kleine-Levin Syndrome | Knobloch Syndrome | Anti-NMDA Receptor Encephalitis | Colitis | Pontocerebellar Hypoplasia Type 2 | Deafness, Dystonia, And Cerebral Hypomyelination | Hyperlipidemia, Familial Combined | Glutaric Aciduria Type 2 | Herpes Genitalis | Triple A Syndrome | Tracheal Disorders | Hepatic Veno-occlusive Disease | Myofibrillar Myopathy | Hepatic Adenomatosis | Anti-glomerular Basement Membrane Disease | Cystitis, Interstitial | Myopathy | Syphilis | Cornelia De Lange Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Renal Tubular Acidosis | Palmoplantar Keratoderma | Papulopustular Rosacea | Retinal Detachment | Glomerulonephritis | Smoldering Myeloma | CHARGE Syndrome | High Molecular Weight Kininogen Deficiency | Progressive Familial Intrahepatic Cholestasis Type 2 | Spondyloperipheral Dysplasia | Botulism | Aphasia | Torticollis | Dystrophy, Cone-rod | Nicotine Addiction | Pituitary Stalk Interruption Syndrome | Spinocerebellar Ataxia Type 5 | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Epilepsy Of Infancy With Migrating Focal Seizures | Prurigo Nodularis | GLUT1 Deficiency Syndrome | Bronchitis | Trachoma | Tendinitis | Keratoconus | Keratoconjunctivitis | X-linked Sideroblastic Anemia | Sleep Apnea | Wagner Disease | Retinal Coloboma | Peripheral T-cell Lymphoma | Emery-Dreifuss Muscular Dystrophy | Chiari Malformation Type I | Familial Glucocorticoid Deficiency | Acute Leukemia | Connective Tissue Disorders | Hemimegalencephaly | Cancer, Brain | Periodontitis | Fahr Disease | Paraganglioma | Spondyloarthritis | Citrullinemia | Familial Hypobetalipoproteinemia | Neuroectodermal Tumors, Primitive | Hepatitis D | Neurogenic Bladder | Polyomavirus Nephropathy | PHARC Syndrome | Intermittent Explosive Disorder | Hypogonadism | Vitreoretinal Degeneration, Snowflake Type | Schistosomiasis | Chondroma | Chronic Myelomonocytic Leukemia | Colitis, Collagenous | Scapuloperoneal Spinal Muscular Atrophy | WAGR Syndrome | L-2-Hydroxyglutaric Aciduria | Primary Progressive Aphasia | Pulmonary Alveolar Proteinosis | Angiomyolipoma | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Trimethylaminuria | Retinitis Pigmentosa 3 | Allan-Herndon-Dudley Syndrome | Craniometaphyseal Dysplasia | Axenfeld-Rieger Syndrome | Idiopathic Multicentric Castleman Disease | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Hemorrhage | Postpartum Depression | Sialidosis | Anuria | Spinocerebellar Ataxia Type 27 | Blepharospasm | Cousin Syndrome | Malnutrition | Progressive Familial Intrahepatic Cholestasis | Narcolepsy | Inflammatory Myofibroblastic Tumor | Encephalopathy, Hepatic | Dermatitis Herpetiformis | Osteoarthritis | Weill-Marchesani Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Hepatitis, Autoimmune | Urticaria | Gerodermia Osteodysplastica | Glutathione Synthetase Deficiency | Ornithine Transcarbamylase Deficiency | Focal Dermal Hypoplasia | Dowling-Degos Disease | Metaphyseal Chondrodysplasia, Schmid Type | Agoraphobia | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Fetal And Neonatal Alloimmune Thrombocytopenia | Spinal Cord Diseases | Burn-McKeown Syndrome | Hypertensive Retinopathy | Binge Eating Disorder | Hepatoblastoma | Pilomatrix Carcinoma | Membranous Nephropathy | LMNA-related Congenital Muscular Dystrophy | Thrombosis | Granular Corneal Dystrophy Type 1 | Primary Aldosteronism | Craniofrontonasal Syndrome | Galloway-Mowat Syndrome | Tremor | Micropenis | Cutaneous Mastocytosis | Choroiditis | Carcinoma, Signet Ring Cell | Lymphangioleiomyomatosis | Blood Protein Disorders | Retinal Dystrophy | Corneal Dystrophies, Hereditary | Succinic Semialdehyde Dehydrogenase Deficiency | Scabies | Menetrier Disease | 3-methylglutaconic Aciduria Type I | Idiopathic Pulmonary Fibrosis | Colorectal Adenoma | Erysipelas | Becker Muscular Dystrophy | Episodic Ataxia Type 1 | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Oculocutaneous Albinism Type 1 | Paroxysmal Nocturnal Hemoglobinuria | Lymphoma | Orotic Aciduria | Contact Dermatitis | Graves Disease | Vogt-Koyanagi-Harada Syndrome | Osteopathia Striata With Cranial Sclerosis | Beta-Propeller Protein-associated Neurodegeneration | Usher Syndrome Type IIC | Arterial Tortuosity Syndrome | Goiter, Nodular | Hydrolethalus Syndrome | Non-Langerhans Cell Histiocytosis | Autosomal Recessive Spastic Paraplegia Type 54 | Congenital Hemolytic Anemia | GM2-gangliosidosis AB Variant | Schuurs-Hoeijmakers Syndrome | Krabbe Disease | Carotid Artery Disease | Oculocutaneous Albinism | Behavioral Variant Of Frontotemporal Dementia | Hyperbilirubinemia, Neonatal | Hyperthyroidism | Gastritis | Compartment Syndrome | Cannabis Abuse | Tyrosinemia Type 2 | Basal Ganglia Cerebrovascular Disease | Coenzyme Q10 Deficiency | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Neurofibromatosis Type 1 | Spinocerebellar Ataxia Type 14 | Marinesco-Sjogren Syndrome | Epidermolytic Palmoplantar Keratoderma | Takayasu's Arteritis | Schnyder Crystalline Corneal Dystrophy | Acanthosis Nigricans | Incontinentia Pigmenti | Waardenburg Syndrome | Gardner Syndrome | DNA Ligase IV Deficiency | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Epidermolysis Bullosa | Ureteropelvic Junction Obstruction | Bainbridge-Ropers Syndrome | Polymicrogyria | Chondrodysplasia Punctata | Gitelman Syndrome | Carcinoma, Transitional Cell | Tibial Muscular Dystrophy | Macular Corneal Dystrophy Type 1 | Pseudohypoparathyroidism Type 1C | Muir-Torre Syndrome | Keloid | Cardiospondylocarpofacial Syndrome | Rhabdomyosarcoma, Alveolar | Patent Ductus Arteriosus | Stevens-Johnson Syndrome | Follicular Dendritic Cell Sarcoma | Bernard-Soulier Syndrome | Cystinosis | Epilepsy, Generalized | Crouzon Syndrome With Acanthosis Nigricans | Bullous Pemphigoid | Megaloblastic Anemia | Nephrocalcinosis | Thyroiditis | Neurofibromatosis-Noonan Syndrome | Parvovirus B19 Infection | Reticular Dysgenesis | Esthesioneuroblastoma | Spondylocostal Dysostosis | Exostoses | Rett Syndrome | Hypercholesterolemia | Alagille Syndrome | Achondrogenesis | Kabuki Syndrome 2 | Heroin Dependence | Metatropic Dysplasia | Hypogammaglobulinemia | Rickets | Generalized Epilepsy With Febrile Seizures Plus | Fanconi Anemia | Central Pain Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Oligoastrocytoma | Albinism | Low Phospholipid Associated Cholelithiasis | Speech Disorders | Periventricular Leukomalacia | Macrophage Activation Syndrome | Williams Syndrome | Iron Metabolism Disorders | Chromosome 9q34.3 Deletion Syndrome | Diabetes Mellitus, Transient Neonatal | Granular Corneal Dystrophy | Sclerosing Cholangitis | Hydrocephalus | Distal Spinal Muscular Atrophy | Dysfibrinogenemia | Pulmonary Capillary Hemangiomatosis | DiGeorge Syndrome | AIDS | Sengers Syndrome