Disease

Multiple Myeloma

About the Disease
Myeloma, Multiple, also known as multiple myeloma, is related to monoclonal gammopathy of uncertain significance and plasma cell neoplasm. An important gene associated with Myeloma, Multiple is LIG4 (DNA Ligase 4), and among its related pathways/superpathways are Breast cancer pathway and MAPK Signaling: Mitogens. The drugs Busulfan and Levofloxacin have been mentioned in the context of this disorder. Affiliated tissues include Blood, and related phenotypes are osteopenia and pathologic fracture

Common Targets
HLA-C | HMOX1 | TCF7L2 | NACAD | LILRB1 | KLRC1 | CDK4/Cyclin D3 | DEPDC5 | BCLAF1 | SCN5A | ZC3H11C | ETS2 | G238 | RPS6KA4 | GSTP1 | TNFRSF9 | JAK3 | KCNJ11 | FOXD4L6 | MIR221 | TNFRSF10B | JAK1 | PSMD1 | LCE1D | Mitogen-activated protein kinase p38 (MAPK p38) (nonspecified subtype) | CHEK2 | CIP2A | HTR7 | IL2RB | SELE | G6647 | MYNN | LOC107986598 | HLA-DQB1 | YES1 | DTX2 | MIR149 | MAGEA3 | KDM5B | G596 | SRP54-AS1 | ICOS | G6714 | NFKB1 | CRBN | TOMM40L | ADGRB3 | KDR | XRCC1 | NTRK2 | HCK | CTNNB1 | MAP3K12 | BCAM | MIR222 | NAALADL1 | APOA2 | DNA Methyltransferase (DNMT) (nonspecified subtype) | LRP6 | ABHD18 | IL6ST | SP3 | ERCC5 | FGR | RUNX2 | CD74 | POT1-AS1 | STN1 | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | G472 | COPZ2 | CD247 | Killer Cell Immunoglobulin-Like Receptor (KIR) (nonspecified subtype) | Protein farnesyltransferase | CARM1 | LOC105377369 | MUC17 | AURKA | PXK | Cyclin B (nonspecified subtype) | CDK4/Cyclin D1 | NCAN | USP17L25 | CD24 | PRC1 | MRPL22 | PSMB5 | DNA-Directed DNA Polymerase Complex | Integrin alpha4beta1 (VLA-4) receptor | G1956 | ELL2 | ABL1 | TMPRSS13 | NBPF1 | SEZ6 | PADI4 | HDAC10 | GSR | ADRM1 | RIC8A | SDC1 | G3845 | CTB-30L5.1 | MALT1 | IL-15 receptor | EPHB2 | TRIP13 | HLA-E | JAK2 | POTEF | XPC | SOCS1 | G3309 | IL1B | LOC105373220 | FBRS | NISCH | ANKRD20A3P | SNIP1 | AKAP9 | IGSF3 | MAGEA4 | CEP162 | POU2F1 | PPIAL4G | NUTM2G | EOMES | CRY2 | AQP7 | MADD | gamma-Secretase | SPDYE1 | ASPM | G6774 | MOCOS | ELFN2 | RASA1 | PPIAL4A | ERCC1 | EXT2 | PSMB9 | MAGEC1 | IL1RN | MAX | TFRC | G6PC2 | NR1I3 | G3569 | CSK | CDK2 | Geranylgeranyl transferase type-1 | FCRLA | ABCA10 | HDAC8 | TMEM132B | G7015 | TRAF3 | HDAC6 | TNFSF13 | PAK2 | SPHK2 | CYP2D6 | SMO | Cyclin-dependent kinase (nonspecified subtype) | ERCC6 | VILL | IKBKB | ZNF705A | NFKB2 | SOST | CTC1 | LGALS3 | CCDC169-SOHLH2 | TRPM6 | AMP-activated protein kinase (AMPK) | FGFR2 | TNFRSF10A | PKN2-AS1 | IFI44L | Integrin alphavbeta3 (vitronectin) receptor | CYP2C19 | CTAG1A | ZFP82 | HDAC2 | G59272 | CDK5/p25 | DAB2 | CCND2 | Inhibitor of Apoptosis Proteins (IAPs) (nonspecified subtype) | BTK | NAE1 | E3 ubiquitin-protein ligase (nonspecified subtype) | AGAP4 | BPIFB6 | NCAM1 | HIF1A | Heat shock protein 90 (nonspecified subtype) | ACADVL | MIR137 | HOXB13 | TCF19 | FAT1 | TMEM150B | TRAC | KMT2C | IL17RA | HMOX2 | TBC1D3G | G1/S-specific cyclin-E (nonspecified subtype) | CNR2 | STAT6 | ELANE | MYO10 | G595 | GADD45B | SLC3A2 | FBXL6 | DCUN1D1 | T-Type Calcium Channel | IL10RA | LY9 | FKBP1A | USP17L11 | IRAK3 | Hedgehog Protein (nonspecified subtype) | TGFB1 | NPM1 | GCK | CDK6 | ADAMTS5 | ANKRD36 | G207 | CCDC9 | CCR7 | Ephrin Receptor (nonspecified subtype) | IL-1 Receptor (nonspecified subtype) | G1432 | LTA | NRAS | CHEK1 | Protein Kinase B (PKB/Akt) (nonspecified subtype) | ADP-Ribosyl Cyclase/cyclic ADP-Ribose Hydrolase (ADPRC) (nonspecified subtype) | KRTAP5-4 | AURKB | URB1 | RPSAP52 | HLA-DQA1 | SP140 | LCK | NF-kappaB (NFkB) | UNC13D | POLE | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | G7099 | Transforming growth factor (nonspecified subtype) | Ribonucleoside-diphosphate reductase | G3479 | SLC22A3 | BMX | LAG3 | CTAGE4 | LOC102724428 | ATG5 | Lipoxygenase (nonspecified subtype) | BRD2 | CILP2 | Protein kinase C (nonspecified subtype) | MUTYH | CDKAL1 | GRIK2 | TYK2 | LAMP5 | EBF3 | G842 | G598 | EFCAB5 | G1950 | TRIM35 | CSF1R | PIM3 | MMP12 | TNFRSF18 | TBCE | MAOA | TNFSF13B | mTOR complex 1 | AFP | G5133 | Fibroblast growth factor (FGF) (nonspecified subtype) | GREB1L | WAC | SOX2 | MIR34B | G7295 | CDK5 | SLAMF7 | SPARC | APOBEC3H | CD3 Complex (T Cell Receptor Complex) | DHODH | TP73 | MIR375 | IGFN1 | SPDYE5 | GDF2 | TUBA3E | TNFSF11 | PDIA6 | MAP3K14 | DLC1 | HSF1 | TNFAIP2 | G4780 | TOM1 | GPRC5D | IL3RA | SMPD1 | TOP1 | TRPM8 | IKZF1 | CD86 | SF3B1 | FLRT2 | CDK4 | TIRAP | KIT | CDK11A | CCHCR1 | G29126 | HLA-B | CD48 | BTNL2 | RRAGD | IL10RB | PIK3CB | POU5F1 | TMEM132D | CDK9/Cyclin T1 | CLEC11A | SKA3 | HDAC11 | USP14 | CYP1A1 | SULT1E1 | CD200 | DDR2 | GPC1-AS1 | ST3GAL6-AS1 | ARG1 | CDH8 | COL5A1 | G7852 | TAS1R2 | UCHL5 | BRCA2 | GFRA1 | ICAM1 | CLIP1 | DRD2 | VCAM1 | G23411 | BCR | LAMC1 | POTEB2 | ULK4 | MAP2K1 | XIAP | PRAMEF9 | CNR1 | CYP2C8 | LGALS9 | ABCA1 | PRAMEF14 | FGFR3 | OGG1 | BRD4 | TM6SF2 | RAD23B | ZFHX3 | DKK1 | HAS1 | HLA-DRB1 | KRTAP5-8 | NR1I2 | PSMB11 | PIK3CD | NPM3 | GOLGA6D | TK2 | OR2H2 | CCN2 | CDKN2B-AS1 | PRSS3 | AGAP11 | DNA Topoisomerase II (nonspecified subtype) | TSC2 | TRPV2 | CDC27 | ACTRT3 | SRCAP | IL15 | G673 | TBL1XR1 | HDAC3 | PTCH2 | CDK9 | CD44 | ARAP1 | STT3B | MSI1 | Casein kinase II (CKII) | IRF4 | ENTPD3 | SLAMF6 | Histone acetyltransferase (HAT) (nonspecified subtype) | ZAP70 | FAM205A | CD52 | AHSA1 | CD38 | SIRPA | Integrin alphavbeta5 receptor | MIR34C | XPO1 | PSMB1 | CD40 | HRNR | CYP24A1 | CEACAM8 | FOXA1 | Interleukin-12 (IL-12) | NTRK3 | P3H2 | LOC105378110 | ABCC2 | G142 | KLRK1 | SLC22A15 | Pim Kinase (nonspecified subtype) | CCAT1 | MAPKAPK2 | LILRB3 | CDK6/Cyclin D1 | INSR | NCS1 | GCKR | CES1 | ADORA2A | OR6B3 | ICAM5 | ZDHHC8 | ADCY5 | RFC3 | LRRC37A3 | TRPV1 | PDGFRB | GPC1 | G1029 | RBMS1 | GOLGA6L9 | TGFBR1 | EIF5A | DNAH11 | Reverse transcriptase (Telomerase) | G3605 | DOCK1 | GRK4 | Tyrosine Kinase (nonspecified subtype) | TLE1 | MUC1 | ANKRD26 | UHRF1 | HDAC1 | PTCH1 | SUMO activating enzyme complex | G4170 | XDH | DNAJC16 | ANKRD36B | FCGR3A | PPARG | FCGBP | CCNT1 | PTGS1 | TRIM71 | KRT81 | PLAT | KLF2 | SLC22A2 | C7 | FYB1 | OR2T3 | ADORA3 | SPATA31A6 | PSORS1C1 | KRTAP4-6 | PDE4DIP | NEDD8-activating enzyme E1 | AKT2 | G4609 | WFS1 | SERPINE1 | CDKN2C | CASP8 | UBXN7 | ACVR1 | BIRC3 | JAZF1 | G920 | PREX1 | RYR2 | NTRK1 | ATP6V1B2 | RHPN2 | Heme Oxygenase (HO) (nonspecified subtype) | CT47B1 | LRRC34 | G999 | POTEE | ADAMTS9-AS2 | KCNA6 | DEFB104B | GPX3 | HLA-A | PSORS1C2 | MEN1 | ACKR3 | RBP1 | FBXW10B | SMARCD3 | AEBP1 | FDPS | GAB2 | BCL2A1 | SELPLG | XRCC3 | TRNT1 | TRBV3-1 | G9429 | GABBR2 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | DRD1 | TNFAIP3 | CD70 | PRSS41 | CXCL12 | EPHA4 | G2475 | CD1D | MS4A1 | CHUK | CEP20 | S100A9 | TBC1D3C | OR10G9 | MFAP3L | HOXB4 | HSD17B13 | DAPK1 | AURKC | NEFM | PTCSC2 | GSTT1 | XPO5 | CDK1/Cyclin B | G3480 | G6PC1 | APOBR | PSMC2 | mTOR complex 2 | G3630 | MALAT1 | EPHB6 | CHIA | TNFRSF11A | UBE2M | SETD2 | EPOR | PRAMEF6 | FLT4 | DEFB105B | ACOXL | CD33 | HDAC4 | CCR1 | ING4 | NCR3 | CCND3 | KIR2DL1 | Vascular endothelial growth factor receptor (VEGFR) (nonspecified subtype) | PSMB2 | IKZF3 | ABCC6 | KMT2A | FBXW10 | IDH2 | KIF11 | G2033 | MMP13 | Transforming growth factor beta (nonspecified subtype) | CKS1B | CLCN4 | NSD2 | CR1 | MLL/SET1 Complex | LAMA2 | KDM1A | DLL1 | CD80 | FRK | ZBTB20 | PPP2R5E | Mitogen-Activated Protein Kinase (nonspecified subtype) | SEM1 | H1-3 | Platelet-Derived Growth Factor Receptor (nonspecified subtype) | MIB2 | TSPAN32 | GYS1 | ZBTB46 | FGF1 | G836 | ADAMTS4 | RAD51 | HBG1 | CHI3L1 | RORB | EEF1A2 | FGFR1 | FLT1 | KLRC4-KLRK1 | GLUL | TNFRSF13C | G4318 | CD3E | DCLK1 | BCL2L2 | CDK2/Cyclin A | CCNE1 | Heat shock protein 70 (nonspecified subtype) | KCNQ1 | GRK5 | NR3C1 | RAF1 | Ikzf1 | OASL | TP53INP1 | TNFRSF17 | DIS3 | HYDIN | APEX1 | AP-1 Transcription Factor Complex | MYH6 | SIK2 | BSN | BLK | CEP120 | KIR2DL2 | TEK | OR6Q1 | FGFR4 | CLPP | BMP10 | SALL4 | Janus Kinase (nonspecified subtype) | ERN1 | PRKCB | G7157 | ZNF658 | Glutaminase (nonspecified subtype) | PRKRA | HK2 | DDR1 | RB1 | IL16 | DTNB | PIM1 | Inosine 5'-monophosphate dehydrogenase (IMPDH) (nonspecified subtype) | CTSK | NOS3 | IRF8 | VCP | A1CF | RPA1 | CSF2RA | CCSER1 | EPHA5 | BRD3 | OR51V1 | G4193 | PSMB8 | IL2 | CBX7 | ENTPD1 | EIF2AK3 | ACYP2 | MUC4 | MPEG1 | PCDHB8 | CTAG1B | TNFRSF4 | ZNF717 | CXCR2 | METAP2 | HRH1 | PHB2 | WDFY3 | CDK2/Cyclin E | Sphingolipid delta(4)-desaturase (nonspecified subtype) | LYN | ARHGAP45 | PDE5A | RIC1 | SOHLH2 | Focal Adhesion Kinases (FAK) (nonspecified subtype) | TIGIT | HPSE | KIR2DL3 | DDB1 | CDK6/Cyclin D3 | DPY19L2 | PSMD5 | SIK1 | UTRN | SYNE1 | PROX1 | NHLRC3 | Tubulin | G1786 | MMP2 | EPRS1 | G3082 | CEP170 | Cyclin-dependent kinase inhibitor (nonspecified subtype) | MAP2K2 | RALGAPA1 | G5743 | EPHX1 | 5-Hydroxytryptamine Receptor (nonspecified subtype) | SLC2A2 | XRCC5 | Cyclin A (nonspecified subtype) | Tumor Necrosis Factor Receptor Superfamily Member 10 (TRAIL-R) (nonspecified subtype) | PLIN4 | VDR | NT5E | TLR9 | ROBO1 | SH3BP2 | SYT11 | PARP2 | RIPK3 | TYMS | NOS2 | LRP1B | G4233 | MAPK7 | NOTCH2 | HLA-DRB5 | XPA | PROX1-AS1 | CFTR | DEGS2 | SAA2 | CTLA4 | WT1 | CDCA7L | CD47 | LILRB5 | ATP6AP1 | BST2 | CD28 | SLC7A10 | IGF2BP2 | CCR5 | PIK3CA | DEGS1 | TRPA1 | DDX55 | LIG3 | SLC30A8 | MIF | MST1 | CT47A10 | DOCK9 | ALB | GOLGA8O | NBPF10 | FTO | AKT3 | CYP1B1 | ABCC1 | ZDHHC9 | KMT2D | SLC25A6 | LGALS1 | FYN | BRD9 | G8878 | PAFAH1B2P2 | RFWD3 | CREBBP | CX3CR1 | AGAP7P | Dual Specificity Mitogen-Activated Protein Kinase Kinase (MEK) (nonspecified subtype) | G7124 | NCOA1 | 11beta-Hydroxysteroid Dehydrogenase (nonspecified subtype) | UMAD1 | CD46 | CDK12 | GSTM1 | RARS2 | BIRC5 | KDM1B | TNFRSF13B | ABCA12 | IRS1 | TERC | IL17RB | ADAM30 | PTPRC | Ribosomal Protein S6 Kinase, 70kDa (p70S6K) (nonspecified subtype) | PRAMEF19 | MUC6 | PDGFRA | IL6R | MIR196A2 | TBC1D3H | FLT3 | ABCC3 | IL10 | DRD3 | MTHFR | FCRL5 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | RET | FADS1 | MAGEA1 | CCNK | MTR | FGF2 | TPTE2 | PSMC5 | IL4 | GRK7 | MYBPC3 | VHL | Proteasome Complex | MGMT | UNG | NEK2 | INPP5D | TOP2A | U2AF1 | IFNAR2 | RHOA | TOGARAM1 | THADA | Histone deacetylase (nonspecified subtype) | G2146 | MYCBP2 | SSPOP | NEK3 | BRDT | PPT1 | ITGB7 | G5243 | CYP19A1 | NCR1 | CDK1 | RIGI | REXO1L1P | STAG2 | IL13 | HNF1B | CDK7 | GPR55 | PIM2 | SLC24A1 | IL18 | TGFBI | CD19 | PSMC6 | CLEC18A | G7422 | PRAME

疾病靶点研报
Multiple myeloma

Note: If you'd like to get a target analysis report for Multiple Myeloma, 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 Multiple Myeloma at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

Other Diseases

6-pyruvoyl-tetrahydropterin Synthase Deficiency | Peeling Skin Syndrome, Acral Type | Bartter Syndrome | Lymphopenia | Reflex Epilepsy | Glomerulonephritis | Carcinoma, Small Cell | Cheilitis | Cholecystitis | Paracoccidioidomycosis | Charcot-Marie-Tooth Disease Type 2T | Myelodysplasia | Imerslund-Grasbeck Syndrome | Apparent Mineralocorticoid Excess Syndrome | Epidermolysis Bullosa Acquisita | Extramammary Paget's Disease | Jacobsen Syndrome | Schuurs-Hoeijmakers Syndrome | Hemolytic Anemia | Basal Ganglia Cerebrovascular Disease | Cryoglobulinemia | Cenani-Lenz Syndactyly Syndrome | Low Phospholipid Associated Cholelithiasis | Echinococcosis | Meconium Ileus | Budd-Chiari Syndrome | Usher Syndrome Type III | Gastritis, Atrophic | Hyperinsulinism-hyperammonemia Syndrome | Alopecia Areata | Chylomicron Retention Disease | Mitochondrial Cytopathy | Retinal Detachment | Duodenal Atresia | Gyrate Atrophy Of The Choroid And Retina | Dementia | Sorsby Fundus Dystrophy | Charcot-Marie-Tooth Disease Type 3 | Familial Advanced Sleep Phase Syndrome | Gray Platelet Syndrome | Schistosomiasis Mansoni | Primary Erythromelalgia | Chronic Kidney Disease | Heart Block | Netherton Syndrome | Mitochondrial Encephalomyopathy | Dyggve-Melchior-Clausen Disease | Polymicrogyria | Sclerosing Cholangitis | Hepatorenal Syndrome | Silver-Russell Syndrome | Renal Tubular Acidosis | Cancer, Brain | Aarskog-Scott Syndrome | Malaria | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Chronic Lymphocytic Leukemia | Thrombocytopenia | Ichthyosis Hystrix, Curth-Macklin Type | Chondrodysplasia Punctata | Gardner Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Nicotine Dependence | Carotid Artery Disease | Hemangioblastoma | Dystonia-parkinsonism, X-linked | Hypopigmentation | Adenoma, Pituitary | Phenylketonuria | Lentigo | Carey-Fineman-Ziter Syndrome | Pseudoexfoliation Syndrome | Restless Legs Syndrome | Isovaleric Acidemia | Synovitis | Alzheimer Disease, Late Onset | Chediak-Higashi Syndrome | Early Infantile Epileptic Encephalopathy 28 | Asphyxia Neonatorum | Eating Disorder | Hoyeraal-Hreidarsson Syndrome | Charcot-Marie-Tooth Disease Type 4E | Infantile Liver Failure Syndrome 1 | Unverricht-Lundborg Syndrome | Birt-Hogg-Dube Syndrome | Sepiapterin Reductase Deficiency | Glycogen Storage Disease Type 0, Muscle | Anovulation | Camurati-Engelmann Disease | Ovarian Hyperstimulation Syndrome | Kernicterus | Zollinger-Ellison Syndrome | Sitosterolemia | Tetraplegia | Acne | Oligoasthenoteratozoospermia | Anorchia | Trichomegaly | Antley-Bixler Syndrome | Coenzyme Q10 Deficiency | Scleritis | Hypolipoproteinemia | Cataract | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Hypersomnia | Emery-Dreifuss Muscular Dystrophy | Micropenis | Congenital Lipoid Adrenal Hyperplasia | Joubert Syndrome | Ectodermal Dysplasia | Evans Syndrome | NDH Syndrome | Chondrosarcoma | Graves Disease | Lupus Erythematosus | Neuroma | Pancreatitis | Mucormycosis | Pigment Dispersion Syndrome | Focal Facial Dermal Dysplasia | Spondylometaphyseal Dysplasia | Cancer, Breast | Hartnup Disease | Cherubism | Orotic Aciduria | Amebiasis | Dysgerminoma | Vitamin B12 Deficiency | Glycogen Storage Disease Type 0 | Priapism | Cysticercosis | Myasthenia Gravis | Chordoma | Idiopathic Multicentric Castleman Disease | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Spinocerebellar Ataxia Type 12 | Farber Disease | Persistent Truncus Arteriosus | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Trichuriasis | Chondromyxoid Fibroma | Crisponi Syndrome | Charcot-Marie-Tooth Disease Type 4 | Hyperkeratosis | Pupil Disorders | Erythropoietic Protoporphyria | Iron Overload | Fuchs Heterochromic Iridocyclitis | Preaxial Polydactyly | Neurodegeneration With Brain Iron Accumulation | Ebstein Anomaly | Empyema | Porencephaly | Multiple Sclerosis, Secondary Progressive | Alpha-thalassemia Myelodysplasia Syndrome | Schindler Disease | Urea Cycle Disorder | Hypertension, Renovascular | Nijmegen Breakage Syndrome | Adenoid Cystic Carcinoma | Shwachman-Bodian-Diamond Syndrome | Pituitary Disorders | Dubin-Johnson Syndrome | Nephronophthisis | Primary Pigmented Nodular Adrenocortical Disease | Hemorrhoids | Enlarged Vestibular Aqueduct | Prader-Willi Syndrome | Iron Deficiency Anemia | Primary Progressive Aphasia | Peters-plus Syndrome | Sickle Cell Anemia | Persistent Hyperplastic Primary Vitreous | Oligoastrocytoma | Hyperparathyroidism, Primary | Episodic Ataxia Type 1 | Ureteropelvic Junction Obstruction | Basal Ganglia Disease | Hypoparathyroidism | Encephalopathy, Hepatic | Zygomycosis | Adenocarcinoma | Platelet Disorders | Methemoglobinemia | Spinocerebellar Ataxia Type 3 | Autoimmune Hemolytic Anemia | Thrombophlebitis | Familial Retinal Arterial Macroaneurysm | Congenital Myopathy | Autosomal Recessive Congenital Ichthyosis | Pulverulent Zonular Cataract | Waardenburg Syndrome Type 1 | Chronic Granulomatous Disease | Corneal Dystrophy And Perceptive Deafness | Aicardi-Goutieres Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | HELLP Syndrome | Low Tension Glaucoma | Azoospermia | Wiskott-Aldrich Syndrome | Dementia, Vascular | Benign Familial Infantile Seizures | Muir-Torre Syndrome | Familial Hypobetalipoproteinemia | Hereditary Inclusion Body Myopathy | Cerebrotendinous Xanthomatosis | Williams Syndrome | Microcephalic Primordial Dwarfism | Conduct Disorder | Rhabdomyosarcoma | Carcinoma, Squamous Cell | Peripheral Neuropathy | Withdrawal Syndrome | Cardiofaciocutaneous Syndrome | Wagner Disease | Medulloblastoma | Nemaline Myopathy | Gastroschisis | Charcot-Marie-Tooth Disease Type 2D | Krabbe Disease | DNA Ligase IV Deficiency | Congenital Disorders Of Glycosylation | Beckwith-Wiedemann Syndrome | Spondylo-ocular Syndrome | Greenberg Dysplasia | Hereditary Sensory Neuropathy Type 1 | Pyruvate Decarboxylase Deficiency | Psoriasis | Carpenter Syndrome | Spinocerebellar Ataxia Type 42 | Myelofibrosis | GAPO Syndrome | Keratitis-ichthyosis-deafness Syndrome | Idiopathic Pulmonary Fibrosis | Methylmalonic Aciduria And Homocystinuria, CblC Type | Oguchi Disease-2 | Angelman Syndrome | Congenital Stromal Corneal Dystrophy | Endometritis | Spinocerebellar Ataxia Type 7 | Lung Diseases | Distal Spinal Muscular Atrophy | Pitt-Hopkins Syndrome | Arteriovenous Malformations | Mucolipidosis Type IV | Spinocerebellar Ataxia Type 15 | Bronchiolitis | Perivascular Epithelioid Cell Tumor | Sporadic Inclusion Body Myositis | Primary Sclerosing Cholangitis | Cavitary Optic Disc Anomalies | Blomstrand Osteochondrodysplasia | Subacute Sclerosing Panencephalitis | Progressive Familial Intrahepatic Cholestasis | Microcephaly, Seizures, And Developmental Delay | Congenital Dysfibrinogenemia | T-cell Chronic Lymphocytic Leukemia | Triphalangeal Thumb-polysyndactyly Syndrome | Retinal Dystrophy | Skin Fragility-woolly Hair Syndrome | Sarcoidosis | Trachoma | Whipple's Disease | Schwannomatosis | Nemaline Myopathy 8 | Papillorenal Syndrome | Ovarian Sex Cord-stromal Tumor | Congenital Dyserythropoietic Anemia Type 4 | Stargardt Disease | Klippel-Feil Syndrome | Sertoli Cell-only Syndrome | Homocystinuria | Vogt-Koyanagi-Harada Syndrome | Wilson's Disease | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Meningococcal Meningitis | Early Infantile Epileptic Encephalopathy 1 | Hypohidrotic Ectodermal Dysplasia | Centronuclear Myopathy | Goiter, Nodular | Thyroid Dyshormonogenesis | Ophthalmoplegia | Hemimegalencephaly | Hypersensitivity Pneumonitis | Orthostatic Intolerance | Spinocerebellar Ataxia Type 31 | Acute Generalized Exanthematous Pustulosis | Otitis Externa | Cholera | Venous Insufficiency | Chronic Leukemia | Congenital Hemolytic Anemia | Mucolipidosis Type III | Mitochondrial Disease | Osteopathia Striata With Cranial Sclerosis | Lysosomal Acid Lipase Deficiency | Cabezas Syndrome | Duane Retraction Syndrome | Pompe Disease | Leiomyosarcoma | Mast Cell Leukemia | Hereditary Elliptocytosis | Actinomycetoma | Cryptococcal Meningitis | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Galloway-Mowat Syndrome | Periodic Limb Movement Disorder | Cutaneous Angiosarcoma | Van Der Knaap Disease | 3-methylcrotonyl-CoA Carboxylase Deficiency | Multiple Sclerosis, Primary Progressive | Choroiditis | Tonsillitis | Bacterial Meningitis | Arts Syndrome | Synpolydactyly | Menetrier Disease | Measles | Chromosome 5q Deletion Syndrome | Angioedema, Acquired | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Fibromyalgia | Juvenile Polyposis | Fabry's Disease | Viral Meningitis | Zellweger Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Thrombosis | Chanarin-Dorfman Syndrome | Acanthosis Nigricans | Cancer, Bladder | Alopecia Totalis | Diabetes Type 2 | Spondylocostal Dysostosis | Rash | Charcot-Marie-Tooth Disease Type 4D | Polycythemia | Arteriosclerosis | Multiple Sclerosis, Chronic Progressive | McLeod Syndrome | Thin Basement Membrane Disease | Basal Cell Nevus Syndrome | Long QT Syndrome Type 2 | Hyperlipidemia, Familial Combined | Juvenile Myoclonic Epilepsy | Galactosemia | Primary Progressive Nonfluent Aphasia | Campomelic Dysplasia | Leishmaniasis, Cutaneous | Adenoma, Villous | Microphthalmia | Bietti Crystalline Dystrophy | Porphyria, Acute Intermittent | Methemoglobinemia Type IV | Lyme Disease | Reticular Dysgenesis | Myocarditis | Macular Degeneration | Acute Tubular Necrosis | Rotor Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Paraplegia | Pelvic Inflammatory Disease | Reye Syndrome | Cholelithiasis | C3 Glomerulonephritis | Fanconi Syndrome | Cancer, Kidney | Uveitis, Anterior | X-linked Acrogigantism | Supravalvular Aortic Stenosis | Dental Caries | Cardiomyopathy, Restrictive | Spondyloepiphyseal Dysplasia Tarda, X-linked | Glioblastoma Multiforme | Infantile Refsum Disease | Diarrhea | Postaxial Polydactyly | Proteasome-associated Autoinflammatory Syndrome 2 | Von Willebrand Disease | Shock, Cardiogenic | Aneurysm, Thoracic Aortic | Stroke | Pfeiffer Syndrome | Ophthalmia, Sympathetic | Biotinidase Deficiency | Autonomic Nervous System Disorders | Open-angle Glaucoma | Schistosomiasis | Osteoporosis | Lymphoma, B-cell | Osteoporosis-pseudoglioma Syndrome | Glycogen Storage Disease | Ileitis | Hypoproteinemia, Hypercatabolic | Androgenic Alopecia | Congenital Central Hypoventilation Syndrome | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Encephalitis | Sleep Disorder