Down Syndrome
Down Syndrome
About the Disease
Down Syndrome, also known as trisomy 21, is related to myeloproliferative syndrome, transient and chromosomal disease. An important gene associated with Down Syndrome is DCR (Down Syndrome Chromosome Region), and among its related pathways/superpathways is MicroRNAs in cardiomyocyte hypertrophy. The drugs Budesonide and Misoprostol have been mentioned in the context of this disorder. Affiliated tissues include thyroid, heart and brain, and related phenotypes are intellectual disability and short neck
Common Targets
NF-kappaB (NFkB) | GABRG2 | MGLL | PIK3R5 | TSPYL5 | UMODL1 | ISLR | TLX1NB | GRIK1 | DPP4 | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | SYNJ1 | DYRK1A | GLIS3 | G7157 | G5594 | Hedgehog Protein (nonspecified subtype) | G7015 | PRRT4 | CHRNA7 | PIGP | PTCH1 | LINC00574 | LINC01426 | BCHE | Neurotrophic Factor (nonspecified subtype) | ASB6 | ABCC5 | NACC2 | MTRR | HOXD10 | PHYHD1 | RNF130 | CLIC6 | CHST6 | Reverse transcriptase (Telomerase) | PDE9A | NMDA receptor | IQSEC3 | G4193 | DSCAM-AS1 | COX4I2 | DENND2C | ZNF212 | HDDC3 | EPS8L1 | CHODL | G4137 | MNX1 | NCAM2 | PLIN3 | CLK4 | FAAH | GART | ITGB2 | MAPK8IP2 | Platelet-Derived Growth Factor Receptor (nonspecified subtype) | FLJ32255 | SLC19A1 | CLU | MCM3AP | TSPO | P2RY6 | Proteasome Complex | PCDH8 | CRBN | NKX6-2 | CHMP3 | TIAM1 | FASN | TTK | TMPRSS2 | PRMT2 | SFTPC | DGUOK | GABRB3 | FGF8 | TLX1 | ESRP2 | APOE | HSPB6 | BCAS2 | AP-1 Transcription Factor Complex | DYRK3 | SMKR1 | MTHFD1 | PNMA8B | PICSAR | PCBP3-AS1 | CYP19A1 | ABHD6 | PHOX2A | QPCT | MX1 | CBS | HLCS | BACE1 | OLIG2 | TCN2 | HTR6 | APP | SLC5A1 | OGA | GABRA5 | SOX9 | PPP5C | CRYAA | RPL11 | COL6A1 | CLK1 | CYYR1 | TRH | RUNX1 | SERINC5 | MTR | MX2 | CNR2 | G1956 | HCCAT5 | ENPEP | DYRK1B | HOXB5 | PCDHGA1 | B2M | SLC37A1 | MTHFR | MIB2 | HOXB6 | LOXL4 | LOC154449 | G3620 | F7 | SHROOM1 | OTOF | YBEY | TMEM176B | G5347 | CLDN14 | Dual-Specificity Tyrosine-(Y)-Phosphorylation Regulated Kinase 1 (nonspecified subtype) | CNR1 | SELENOP | DSCAM | ENOX2 | CSNK1D | ZIC4 | HTR7 | CFAP410 | USH1C | KIF26B | HRCT1 | SIM2 | ACHE | KLHDC7B | CPXM2 | DYRK2 | SNCA | RXFP4 | THBD | SH3BP2 | KDR | TMEM250 | CLK2 | SMO | NALT1 | GABA(A) receptor | SLC51A | ITSN1 | EGFL7 | MXRA8 | LAMC3 | PCP4 | CYYR1-AS1 | SSR4P1 | CSNK1E | PEX10 | PREP | SLC13A3 | SLC18A2 | GPR143 | PITX2 | LOC105372745 | TACC2 | gamma-Secretase | CTHRC1 | LOC105372787 | HOXD3 | CHRM1 | CHRM4 | TSPEAR | LOC105372801 | SLC12A2 | Metabotropic glutamate (mGluR) receptor (nonspecified subtype) | BHMT

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Periventricular Leukomalacia | Primary Hyperoxaluria Type 3 | Idiopathic Pulmonary Fibrosis | Fetal Alcohol Syndrome | Keratoconus | Delirium | SAPHO Syndrome | Tuberculous Meningitis | Long QT Syndrome Type 3 | Periventricular Nodular Heterotopia | Adenomatoid Tumor | Iron Metabolism Disorders | Nicotine Addiction | Proteus Syndrome | Myhre Syndrome | Porphyria, Acute Intermittent | Giant Axonal Neuropathy | Myosin Storage Myopathy | Language Disorders | Communication Disorders | Myelofibrosis | Geleophysic Dysplasia | Waardenburg Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Exostoses | Fuchs Heterochromic Iridocyclitis | Epidermolysis Bullosa Dystrophica | Coronary Artery Disease | Nemaline Myopathy 10 | Thanatophoric Dysplasia | Bronchiectasis | Hypokalemia | Relapsing Polychondritis | Chromosome 5q Deletion Syndrome | Progressive Myoclonic Epilepsy | Robinow Syndrome | Vascular Cognitive Impairment | Borjeson-Forssman-Lehmann Syndrome | Angioedema, 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| Rhabdoid Tumor | Abetalipoproteinemia | Idiopathic Multicentric Castleman Disease | Choroideremia | Niemann-Pick Disease, Type C | Wiedemann-Steiner Syndrome | Osteopathia Striata With Cranial Sclerosis | Congenital Primary Aphakia | Multiple Sclerosis, Chronic Progressive | Aspartylglycosaminuria | Galloway-Mowat Syndrome | Hypertensive Nephropathy | Cancer, Bladder | Phenylketonuria | Spinocerebellar Ataxia Type 1 | Osteitis | Optic Nerve Diseases | Thyroid Dyshormonogenesis | Prune Belly Syndrome | Blue Rubber Bleb Nevus Syndrome | Venous Insufficiency | Urticaria | Hyperkeratosis | Giant Cell Arteritis | Porencephaly | Spinocerebellar Ataxia Type 8 | Androgen Insensitivity | Splenomegaly | Allergic Contact Dermatitis | Anorexia Nervosa | Charcot-Marie-Tooth Disease Type 3 | Hyperostosis | Necrotizing Autoimmune Myopathy | Tylosis With Esophageal Cancer | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Proteasome-associated Autoinflammatory Syndrome 2 | Arthropathy | Pulmonary Vein Stenosis | Waardenburg Syndrome Type 4A | Pyloric Stenosis, Infantile Hypertrophic | Hamartoma | 3-methylglutaconic Aciduria Type IV | Dermatofibrosarcoma | Pericarditis | Glutathione Synthetase Deficiency | Ventricular Septal Defect | Episodic Ataxia Type 1 | Oculocutaneous Albinism | Muscle Wasting | Scapuloperoneal Spinal Muscular Atrophy | Microphthalmia | Keratitis-ichthyosis-deafness Syndrome | Schizophrenia, Paranoid | Esophageal Motility Disorders | Neurocutaneous Syndromes | Plasma Cell Dyscrasia | Takotsubo Cardiomyopathy | Overactive Bladder | LEOPARD Syndrome | Coma | Treacher Collins Syndrome | Acute Kidney Injury | Compartment Syndrome | Primary Aldosteronism | Congenital Heart Block | Senior-Loken Syndrome | Paget's Disease Of The Breast | DOCK8 Immunodeficiency Syndrome | Rhizomelic Chondrodysplasia Punctata | L-2-Hydroxyglutaric Aciduria | Sleep Apnea, Obstructive | Mumps | Cenani-Lenz Syndactyly Syndrome | Congestive Heart Failure | Diabetic Neuropathy | Tracheal Disorders | Milk Allergy | Congenital Dyserythropoietic Anemia Type 1 | Cystinosis | ACTH-independent Macronodular Adrenal Hyperplasia | Harlequin Ichthyosis | Gastrointestinal Disorders | Hepatic Steatosis | Polycystic Liver | Sclerosing Cholangitis | Auriculocondylar Syndrome | Greenberg Dysplasia | Cholelithiasis | Neurofibromatosis-Noonan Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Graves Disease | Usher Syndrome Type IIC | Mountain Sickness | Still Disease | Anosmia, Congenital | Hypokalemic Periodic Paralysis | Fibromyalgia | Lyme Disease | Urolithiasis | Netherton Syndrome | Rothmund-Thomson Syndrome | Pycnodysostosis | Bainbridge-Ropers Syndrome | Speech Disorders | Pulmonary Stenosis | Chronic Enteropathy Associated With SLCO2A1 Gene | Peritonitis | Spermatocele | Stevens-Johnson Syndrome | Apraxia | Familial Hemiplegic Migraine | Cancer, Lung | Spondylosis | Portal Vein Thrombosis | Leiomyosarcoma | Lissencephaly 2 | Hemochromatosis | Macular Corneal Dystrophy | 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Lymphangiectasia-lymphedema Syndrome | Pantothenate Kinase-associated Neurodegeneration | Trimethylaminuria | Lymphedema-distichiasis Syndrome | Progressive Familial Intrahepatic Cholestasis | Gingivitis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Bursitis | Bronchitis, Chronic | Mohr-Tranebjaerg Syndrome | Cryptosporidiosis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Lymphoma | Multiple Sclerosis, Primary Progressive | Fibrosis | Persistent Mullerian Duct Syndrome | Holoprosencephaly | Sclerosteosis 2 | Martsolf Syndrome | Incontinentia Pigmenti | Hydrocephalus | Ocular Hypertension | Congenital Myasthenic Syndrome | Subacute Sclerosing Panencephalitis | Silver-Russell Syndrome | Osteoporosis | Leri-Weill Dyschondrosteosis | Pseudoachondroplasia | Heart Septal Defects | Congenital Disorders Of Glycosylation | Mood Disorder | Hereditary Coproporphyria | Renal Tubular Dysgenesis | Spinocerebellar Ataxia | Autosomal Recessive Bestrophinopathy | Osteomalacia | Pulverulent Zonular Cataract | Guanidinoacetate Methyltransferase Deficiency | Asthma | Jawad Syndrome | Raynaud Phenomenon | Fetal Akinesia Deformation Sequence | Hemochromatosis Type 1 | Familial Episodic Pain Syndrome | Spinocerebellar Ataxia Type 7 | Bicuspid Aortic Valve | Hepatitis, Chronic | Asplenia | Pemphigus | Whipple's Disease | Hypocalcemia | Otitis Externa | Malignant Peripheral Nerve Sheath Tumor | Sezary Syndrome | Dysequilibrium Syndrome | Myasthenia | Hypoalbuminemia | Adenoma, Pituitary | Cardiofaciocutaneous Syndrome | Charcot-Marie-Tooth Disease, Type 6 | Dystonia Musculorum Deformans | Small Lymphocytic Lymphoma | Sarcosinemia | Polymyalgia Rheumatica | Gangliosidosis, GM1 | Nephrotic Syndrome | Sleep Disorder | Parapsoriasis | Distal Myopathy | Antley-Bixler Syndrome | Tardive Dyskinesia | Neurofibroma | Von Hippel-Lindau Disease | Generalized Epilepsy With Febrile Seizures Plus | Hidradenitis Suppurativa | Pulmonary Tuberculosis | Spinal Muscular Atrophy Type 2 | Arteriovenous Malformations | Neuroendocrine Cancer | Combined Pituitary Hormone Deficiency | Klippel-Feil Syndrome | Pulmonary Alveolar Proteinosis | Agoraphobia | Connective Tissue Disorders | Stiff-man Syndrome | Leukocyte Adhesion Deficiency | Tietze Syndrome | Kearns-Sayre Syndrome | Charcot-Marie-Tooth Disease Type 4D | Pheochromocytoma | Hypereosinophilic Syndrome | Echinococcosis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Congenital Diaphragmatic Hernia | C3 Glomerulopathy | Growth Hormone Excess | DRESS Syndrome | Adenoma, Villous | Melanocytic Nevus | Macular Degeneration | Huntington's Disease-like 2 | Pseudohypoparathyroidism Type 1B | Beckwith-Wiedemann Syndrome | Saul-Wilson Syndrome | Tetanus | Anorectal Malformations | Trichuriasis | Vitreoretinopathy, Proliferative | Achondrogenesis | Thyroid Dysgenesis | Meleda Disease | Carpenter Syndrome | Wagner Disease | Progressive Familial Intrahepatic Cholestasis Type 2 | Mosaic Variegated Aneuploidy Syndrome 2 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