AIDS

About the Disease
Acquired Immunodeficiency Syndrome, also known as acquired immune deficiency syndrome, is related to human immunodeficiency virus type 1 and aids dementia complex. An important gene associated with Acquired Immunodeficiency Syndrome is HCP5 (HLA Complex P5), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Ethambutol and Pyrazinamide have been mentioned in the context of this disorder. Affiliated tissues include t cells, breast and bone marrow, and related phenotypes are neoplasm and endocrine/exocrine gland

Common Targets
CARM1 | Serine/Threonine Kinase (nonspecified subtype) | PRMT6 | HDAC8 | HDAC3 | G598 | NF-kappaB (NFkB) | TGFBR1 | POLR1HASP | IFNA13 | ANKRD49 | DPP4 | CDK5 | G6352 | CCR2 | MDK | CDK5/p25 | CTNNA1 | PRMT8 | G7015 | CD40 | G836 | Cyclin-dependent kinase (nonspecified subtype) | ECI2 | MMP2 | CDK9/Cyclin T1 | CDK9 | Protein Tyrosine Phosphatase (PTP) (nonspecified subtype) | NR1I2 | Reverse transcriptase (Telomerase) | ADAM17 | JAK2 | NMDA receptor | Mitogen-Activated Protein Kinase (nonspecified subtype) | G4170 | TLR9 | Casein kinase I (nonspecified subtype) | GM-CSF Receptor (GM-CSF-R) | RAF1 | MASP2 | HDAC11 | IFNG | Histone acetyltransferase (HAT) (nonspecified subtype) | CCNT1 | SELENOF | IL2 | G7099 | Proteasome Complex | Histone deacetylase (nonspecified subtype) | APOBEC3H | PRMT1 | CCR5 | MERTK | CDK11A | PDPK1 | CXCL12 | TEX56P | MRE11 | GAA | KDM1A | GNRHR | CYP2R1 | IL5 | G6PC1 | MAP4K1 | G5133 | GUSB | Interferon alpha/beta Receptor (nonspecified subtype) | G920 | IL4 | AP-1 Transcription Factor Complex | CDK1/Cyclin B | ACVRL1 | G1786 | PIM1 | TACR1 | ELAVL1 | PPP1R11 | EIF5A | Nitric oxide synthase (NOS) (nonspecified subtype) | TSG101 | CDK2/Cyclin A | DHPS | SOAT1 | Sterol O-acyltransferase (ACAT) (nonspecified subtype) | CCR1 | RNF39 | HLA-C | TDO2 | ACE | NT5E | TYRO3 | KRR1 | G5243 | TLR7 | RIPK1 | TNFRSF13C | CDK1 | HDAC6 | CYP2B6 | G1956 | CNR2 | Cyclin A (nonspecified subtype) | IFNAR1 | Rho kinase (ROCK) (nonspecified subtype) | BBC3 | HDAC2 | G595 | POLA1 | G7124 | Cyclin-dependent kinase inhibitor (nonspecified subtype) | HLA-B | APOBEC3G | G3620 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | RAB5A | Phosphodiesterase (nonspecified subtype) | SOAT2 | CDK2 | ACSM4 | CD3 Complex (T Cell Receptor Complex) | CDK4 | G3569 | G5743 | TBK1 | IFNAR2 | CYP27B1 | CDK6 | Tubulin | POLB | VSIR | CYP2C19 | SELE | IKBKE | HDAC1 | PTGS1 | PRMT3 | BRD4 | LINC02571 | PDE4B | PDE7A | RAB27A | Transforming growth factor (TGF)-beta receptor (nonspecified subtype) | CCR3 | PIM2 | Cyclin B (nonspecified subtype) | G7852 | CCRL2 | POLR1H | CSF3 | AXL | IKZF1 | PTPN2 | Lipoxygenase (nonspecified subtype) | RABGGTA | ADORA1 | IL10 | MLKL | Ribonucleoside-diphosphate reductase | DNA Topoisomerase II (nonspecified subtype)

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Other Diseases

Myofibrillar Myopathy | Ophthalmia, Sympathetic | Diffuse Mesangial Sclerosis | Rotor Syndrome | Angiosarcoma | Leukocyte Adhesion Deficiency | Vogt-Koyanagi-Harada Syndrome | Multiple System Atrophy | Marfan Syndrome | Pulmonary Stenosis | Cholera | Agranulocytosis | Alpha-1 Antitrypsin Deficiency | Citrullinemia | GLUT1 Deficiency Syndrome | Eclampsia | Pain | Centronuclear Myopathy | Epilepsy, Generalized | Thrombotic Microangiopathy | Dupuytren Disease | Polymyalgia Rheumatica | Alcoholism | Macrophage Activation Syndrome | Lymphangioma | Malaria | Beckwith-Wiedemann Syndrome | Myopathy | Acrodermatitis Enteropathica | Persistent Hyperplastic Primary Vitreous | Cranial Nerve Disease | Connective Tissue Disorders | Trachoma | Tinea | Myositis | Dysmorphophobia | Tularemia | Adrenal Insufficiency | Lafora Disease | Hennekam Lymphangiectasia-lymphedema Syndrome | Herpes Simplex Dermatitis | Ligneous Conjunctivitis | Erdheim-Chester Disease | Agammaglobulinemia | Cockayne Syndrome | Pneumoconiosis | Malonyl-CoA Decarboxylase Deficiency | Arrhythmogenic Right Ventricular Cardiomyopathy | Frontometaphyseal Dysplasia | Perivascular Epithelioid Cell Tumor | Occipital Neuralgia | Inflammatory Bowel Disease | Blepharospasm | Vitiligo | Angioedema | Thromboembolism | Persistent Fetal Circulation | B-cell Chronic Lymphocytic Leukemia | Pouchitis | Cirrhosis | Chylothorax, Congenital | Paronychia | Glaucoma | Distal Myopathy | Hoyeraal-Hreidarsson Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Hypothalamic Obesity | Congenital Adrenal Hyperplasia | Peripheral T-cell Lymphoma | Sialidosis Type I | Vertebrobasilar Insufficiency | Pernicious Anemia | Haim-Munk Syndrome | Salla Disease | Hypopigmentation | Fundus Albipunctatus | Hepatitis | Hypercholesterolemia | Sleep Apnea | Osteonecrosis Of The Jaw | Myoclonic Atonic Epilepsy | 3-methylglutaconic Aciduria Type I | Multiple Epiphyseal Dysplasia | Multisystemic Smooth Muscle Dysfunction Syndrome | Aneurysm, Thoracic Aortic | Autonomic Nervous System Disorders | Glucagonoma | Tetanus | Crisponi Syndrome | Hypertension, Renovascular | Pituitary Disorders | Carney-Stratakis Syndrome | Non-Hodgkin Lymphoma | Hyperthermia, Malignant | Leukoplakia | Holt-Oram Syndrome | Thrombocythemia, Essential | Spitz Nevus | Intermittent Explosive Disorder | Teratozoospermia | Takotsubo Cardiomyopathy | Melanocytic Nevus | Hemorrhoids | Pierre Robin Syndrome | Waardenburg Syndrome Type 4 | Wolman Disease | Marinesco-Sjogren Syndrome | Double Outlet Right Ventricle | Duodenal Atresia | HELLP Syndrome | Gastritis | Nemaline Myopathy | Keratosis, Seborrheic | Muscle Wasting | Fetal Akinesia Deformation Sequence | Leber Hereditary Optic Neuropathy | Liebenberg Syndrome | Lipodystrophy | Kawasaki Disease | Skin Carcinoma | Beta-Propeller Protein-associated Neurodegeneration | Leukoplakia, Oral | Hypertension | Dysfibrinogenemia | Extramammary Paget's Disease | Tyrosine Hydroxylase Deficiency | Diabetic Neuropathy | Chorioretinitis | Osteogenesis Imperfecta Type III | LRBA Deficiency | Congenital Diaphragmatic Hernia | LEOPARD Syndrome | Colitis, Collagenous | Avellino Corneal Dystrophy | CDKL5 Deficiency Disorder | Peritonitis | Lipid Storage Myopathy | Lymphoma, AIDS-related | Phosphoglycerate Dehydrogenase Deficiency | Aplasia Cutis Congenita | T-cell Prolymphocytic Leukemia | Seizures-scoliosis-macrocephaly Syndrome | Cornelia De Lange Syndrome | Stroke, Hemorrhagic | Glaucomatocyclitic Crisis | Jawad Syndrome | Open-angle Glaucoma | Acrodermatitis | HIBCH Deficiency | Alopecia Areata | Congenital Central Hypoventilation Syndrome | Optic Nerve Diseases | Ehlers-Danlos Syndrome | Perry Syndrome | Seminoma | Hypervalinemia | Nemaline Myopathy 8 | Pyruvate Dehydrogenase Deficiency | Behcet's Disease | Mucolipidosis Type II | Smoldering Myeloma | Hyperuricemic Nephropathy, Familial Juvenile | Juvenile Myoclonic Epilepsy | Plasma Cell Dyscrasia | Acute Lung Injury | Renpenning Syndrome | Nephrocalcinosis | Spinocerebellar Ataxia Type 12 | Glioblastoma | Meniere's Disease | Cardiofaciocutaneous Syndrome | Chitayat Syndrome | Infantile Spasm | Focal Cortical Dysplasia Type 2 | Fanconi Anemia | Ocular Albinism Type 1 | Brugada Syndrome 1 | Hereditary Inclusion Body Myopathy | Galloway-Mowat Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Episodic Ataxia | Benign Recurrent Intrahepatic Cholestasis 1 | Trichomegaly | Hypertension, Pulmonary | Acute Anterior Uveitis | Spinocerebellar Ataxia | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Multiple Sclerosis, Relapsing-remitting | Babesiosis | Hypokalemic Periodic Paralysis | Interstitial Lung Diseases | Neuroectodermal Tumors, Primitive | Pseudoachondroplasia | Diabetes Type 2 | Raine Syndrome | Vitamin K Deficiency | Charcot-Marie-Tooth Disease Type 2D | WAGR Syndrome | Urethritis | Nephronophthisis | Dysplastic Nevus | Hepatitis A | Aphasia | Tendinopathy | Carbamoyl Phosphate Synthetase I Deficiency | Congenital Tufting Enteropathy | Pancreatitis | Hypersensitivity | Menetrier Disease | Orthostatic Intolerance | Creatine Deficiency Syndrome | Neuroleptic Malignant Syndrome | Alagille Syndrome | Alkaptonuria | Hypotonia-cystinuria Syndrome | Congenital Stromal Corneal Dystrophy | Osteoarthritis | Meier-Gorlin Syndrome | Retinitis Pigmentosa | Chronic Leukemia | Thymoma, Malignant | Familial Pheochromocytoma-paraganglioma | Spondylocostal Dysostosis | Sarcoidosis | Crimean-Congo Hemorrhagic Fever | Polyneuropathy | Glutathione Synthetase Deficiency | Tuberculosis | Dysequilibrium Syndrome | Coenzyme Q10 Deficiency | Hyperbilirubinemia, Neonatal | Gestational Trophoblastic Disease | Neuroendocrine Cancer | Cellulitis | Aldosteronism | Opisthorchiasis | Mitochondrial Encephalomyopathy | Basal Ganglia Cerebrovascular Disease | Microcephaly, Seizures, And Developmental Delay | Coffin-Siris Syndrome | Sweet Syndrome | Carcinoid Tumor | Hyperthyroidism | Hypertelorism | Sjogren Syndrome | DiGeorge Syndrome | Osmotic Demyelination Syndrome | Cardiac Arrest | Micropenis | Dentinogenesis Imperfecta | Schizoaffective Disorder | Congenital Absence Of Vas Deferens | Neuromuscular Disorders | Galactosemia | Retinopathy, Diabetic | Sensorineural Hearing Loss | Epithelioid Hemangioma | Ependymoma | X-linked Charcot-Marie-Tooth Disease | Angioimmunoblastic T-cell Lymphoma | Nicolaides-Baraitser Syndrome | Megalencephaly | Parkinson's Disease | Beare-Stevenson Syndrome | Polyradiculopathy | Episodic Ataxia Type 1 | Diabetes | Gastric Atrophy | Coloboma | Leber Congenital Amaurosis | Hyperinsulinemic Hypoglycemia | Anti-glomerular Basement Membrane Disease | Cantu Syndrome | Best Macular Dystrophy | Keratoconus | Lyme Disease | Tyrosinemia Type 2 | Adenoma, Pleomorphic | Endophthalmitis | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Charcot-Marie-Tooth Disease Type 4B1 | Schnyder Crystalline Corneal Dystrophy | Lipid Storage Diseases | Pemphigoid | Nephrosclerosis | Chronic Kidney Disease | Distal Myopathy 2 | Rubeosis Iridis | Papillon-Lefevre Syndrome | Diabetes Insipidus | Seborrheic Dermatitis | Dyslipidemia | Vitreoretinopathy, Proliferative | VACTERL/VATER Association | Charcot-Marie-Tooth Disease Axonal Type 2N | Congenital Bile Acid Synthesis Defect | Neuropathy | Bronchiolitis | Benign Hereditary Chorea | Roberts Syndrome | Hemolytic Anemia | Pneumonia, Mycoplasma | Esophagitis | Mumps | Von Willebrand Disease | GATA2 Deficiency | Spinocerebellar Ataxia Type 8 | Bone Marrow Necrosis | Bronchitis | Ichthyosis Hystrix, Curth-Macklin Type | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | POEMS Syndrome | Xeroderma Pigmentosum | Generalized Epilepsy With Febrile Seizures Plus | Rhabdomyosarcoma | Multiple Sclerosis, Chronic Progressive | Fanconi Syndrome | Schwartz-Jampel-Aberfeld Syndrome | Gardner Syndrome | Tietze Syndrome | Thanatophoric Dysplasia | Imerslund-Grasbeck Syndrome | Pelvic Inflammatory Disease | Conn Syndrome | Central Retinal Artery Occlusion | Relapsing Polychondritis | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Niemann-Pick Disease | Epidermolysis Bullosa Simplex, Localized | Systemic Lupus Erythematosus | Hypertensive Retinopathy | Keratitis-ichthyosis-deafness Syndrome | Waardenburg Syndrome Type 2 | Cholestasis, Intrahepatic | Subcortical Band Heterotopia | Dubin-Johnson Syndrome | Hypobetalipoproteinemias | Polymyositis | High Molecular Weight Kininogen Deficiency | Carcinoid Syndrome | McLeod Syndrome | Bartsocas-Papas Syndrome | Esophageal Motility Disorders | Otitis Media | VACTERL Association | Thrombophilia | Toxic Epidermal Necrolysis | Epiphyseal Chondrodysplasia, Miura Type | Acromegaly | Shock, Cardiogenic | Hemochromatosis Type 2 | T-cell Lymphoma, Subcutaneous Panniculitis-like | Erythropoietic Protoporphyria | Spondylometaphyseal Dysplasia | Pearson Syndrome | Gyrate Atrophy Of The Choroid And Retina | Epidermolysis Bullosa Simplex, Generalized | Yellow Fever | Congenital Muscular Dystrophy | Lichen Planus | Delayed Sleep Phase Syndrome | Pulmonary Veno-occlusive Disease | Charcot-Marie-Tooth Disease Type 3 | Ameloblastoma | Pterygium | Hyperkalemic Periodic Paralysis | Bethlem Myopathy | Hyperferritinemia-cataract Syndrome | Sengers Syndrome | Charcot-Marie-Tooth Disease Type 4E | Asthma, Exercise-induced | Bipolar Disorder | Glycogen Storage Disease Type 0, Muscle | Inflammatory Linear Verrucous Epidermal Nevus | Giant Cell Arteritis | Leishmaniasis, Cutaneous | Glycogen Storage Disease Type 1a | Hemorrhage | Knobloch Syndrome | Infantile Refsum Disease | Encephalitis, Tick-borne | Antithrombin III Deficiency | Nance-Horan Syndrome | Takayasu's Arteritis | Familial Mediterranean Fever | ADNP Syndrome | Arthritis, Gouty | Tenosynovial Giant Cell Tumor | Paroxysmal Nocturnal Hemoglobinuria | Pregnancy, Ectopic | Osteitis | Lissencephaly 2 | Alazami Syndrome | Dental Caries | Polydactyly | Transient Bullous Dermolysis Of The Newborn | Loeys-Dietz Syndrome Type 4 | Arts Syndrome | Carbohydrate Metabolism Disorders | Stomatitis