AIDS
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)
![疾病靶点研报](../img/disease-target-analysis-report.jpg)
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Other Diseases
Meniere's Disease | Shwachman-Bodian-Diamond Syndrome | Retinal Telangiectasia | Cystinuria | Dyslexia | Vitamin K Deficiency | Hemophilia | Adenoma, Pituitary | Obsessive-compulsive Disorder | Light Chain Amyloidosis | Congenital Central Hypoventilation Syndrome | Cerebrovascular Disorders | Malignant Fibrous Histiocytoma | Angioedema | Vitreoretinopathy, Proliferative | Seizures | Atrial Septal Defect | Mosaic Variegated Aneuploidy Syndrome 2 | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Chloridorrhea, Congenital | Polyomavirus Nephropathy | Thrombotic Microangiopathy | Neuroleptic Malignant Syndrome | Hereditary Spherocytosis | Uveitis, Anterior | Protein C Deficiency | Histiocytic Sarcoma | Stickler Syndrome | Blepharophimosis Syndrome | Alagille Syndrome | Frank-ter Haar Syndrome | Intellectual Disability, Autosomal Dominant 5 | Colon Adenoma | Micropenis | Partington Syndrome | Emery-Dreifuss Muscular Dystrophy | Homocystinuria | Fraser Syndrome | Pulmonary Vein Stenosis | Riboflavin Transporter Deficiency Neuronopathy | Glycogen Storage Disease Type 1a | Neurocysticercosis | Spinocerebellar Ataxia Type 42 | Dystonia Musculorum Deformans | Spinocerebellar Ataxia Type 1 | Leiomyoma | Brachydactyly | Eating Disorder | Proteus Syndrome | Sporadic Hemiplegic Migraine | Polydactyly | Greenberg Dysplasia | Osteochondroma | Nephronophthisis | Sensory Neuropathy | Schwartz-Jampel-Aberfeld Syndrome | Glaucoma | Atherosclerosis | Holoprosencephaly | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Inflammatory Joint Disease | Ocular Hypertension | Spinocerebellar Ataxia Type 21 | Branchiootorenal Syndrome | Spinocerebellar Ataxia Type 28 | Exotropia | Astigmatism | Porphyria, Variegate | Sporadic Inclusion Body Myositis | Costello Syndrome | Congenital Heart Defects | Ameloblastoma | Hepatitis E | Familial Hemiplegic Migraine | Pseudohypoparathyroidism Type 2 | Ileitis | Motion Sickness | Chorea-acanthocytosis | Kabuki Syndrome 2 | Acute Kidney Injury | Long QT Syndrome Type 1 | Vascular Cognitive Impairment | Oligospermia | Liddle Syndrome | Galactosemia | Thrombophilia | Endometriosis | Atrioventricular Septal Defect | Specific Granule Deficiency | Hypoglycemia | Eczema | Schizophrenia | Nephritis, Interstitial | Shprintzen-Goldberg Syndrome | Congenital Mirror Movements | Farber Disease | Pseudohypoparathyroidism Type 1C | Babesiosis | Knobloch Syndrome | Glycogen Storage Disease Type 4 | Leukemia-lymphoma, Adult T-cell | Creutzfeldt-Jakob Disease | Spinocerebellar Ataxia Type 5 | Cholangitis | Ataxia-ocular Apraxia 2 | Chondroma | Disseminated Intravascular Coagulation | Methylmalonic Aciduria And Homocystinuria, CblC Type | Ependymoma | Melanoma, Malignant | Oguchi Disease-2 | Hypothyroidism | Chronic Beryllium Disease | Multiple Epiphyseal Dysplasia | Charcot-Marie-Tooth Disease Type 4D | Myelomeningocele | Atopic Dermatitis | Cancer, Lung | Adenomyosis | Hennekam Lymphangiectasia-lymphedema Syndrome | Kawasaki Disease | Aplastic Anemia | Pseudomyxoma Peritonei | Nicolaides-Baraitser Syndrome | Cystitis, Interstitial | Muscular Dystrophy | Relapsing Polychondritis | Heroin Dependence | Adenosine Deaminase 2 Deficiency | Epidermolytic Ichthyosis, Annular | Spondyloepiphyseal Dysplasia Tarda, X-linked | Raine Syndrome | Waardenburg Syndrome Type 2A | Trigonocephaly | Bietti Crystalline Dystrophy | 3-methylglutaconic Aciduria Type IV | Proopiomelanocortin Deficiency | Anovulation | Milk Allergy | Charcot-Marie-Tooth Disease Type 4B1 | Polycythemia Vera | C3 Glomerulonephritis | Thrombosis | Synovitis | Charcot-Marie-Tooth Disease Type 4E | Niemann-Pick Disease | Granuloma Annulare | Pneumothorax | Ichthyosis Hystrix, Curth-Macklin Type | Carcinoma, Signet Ring Cell | Primary Erythromelalgia | Microphthalmia | Hereditary Hemorrhagic Telangiectasia Type 2 | Osteogenesis Imperfecta Type III | Spinocerebellar Ataxia Type 8 | Cardiofaciocutaneous Syndrome | Dementia | Photosensitivity | Hydrolethalus Syndrome | Bicuspid Aortic Valve | 5-oxoprolinase Deficiency | Juvenile Xanthogranuloma | Nicotine Addiction | Systemic Lupus Erythematosus | Periventricular Nodular Heterotopia | Spinal Muscular Atrophy Type 2 | Scoliosis | Melnick-Needles Syndrome | Hemolytic Uremic Syndrome | Primrose Syndrome | Hemangioma | Congenital Hypofibrinogenemia | Hypertrophy | Congenital Tufting Enteropathy | Larsen Syndrome | Avian Influenza | Esophageal Carcinoma | HANAC Syndrome | Focal Cortical Dysplasia Type 2 | Hypertension | Pancreatitis, Chronic | Keratosis, Actinic | Pierpont Syndrome | Encephalopathy, Glycine | Alopecia Areata | Otitis Media | Schindler Disease | Paraganglioma, Carotid Body | Congenital Fiber-type Disproportion Myopathy | Meckel-Gruber Syndrome | Neural Tube Defect | Tangier Disease | Idiopathic Multicentric Castleman Disease | Migraine | Progressive Familial Intrahepatic Cholestasis Type 1 | Genitopatellar Syndrome | Meningococcal Infections | Nail Disorder, Nonsyndromic Congenital | Hyperthyroidism | Chylothorax, Congenital | Oculocutaneous Albinism Type 2 | Mastitis | Adrenoleukodystrophy, X-linked | Osteogenesis Imperfecta Type I | Panuveitis | Glioblastoma Multiforme | Androgenic Alopecia | Fatty Aldehyde Dehydrogenase Deficiency | Mitochondrial Myopathy | Zimmermann-Laband Syndrome | Vitreoretinal Degeneration, Snowflake Type | Epidermolysis Bullosa | Renal Oncocytoma | Pyruvate Kinase Deficiency | Amelogenesis Imperfecta | Tinea Versicolor | Syndactyly | Auriculocondylar Syndrome | Chronic Periodontitis | Alexander Disease | Chronic Neutrophilic Leukemia | Kaposi Sarcoma | Familial Episodic Pain Syndrome | Canavan Disease | Headache | Porphyria Cutanea Tarda | Spinal Muscular Atrophy Type 3 | Spinocerebellar Ataxia Type 23 | Metachondromatosis | Polycythemia | Erythrokeratodermia Variabilis | Acne Vulgaris | Nemaline Myopathy 10 | Dowling-Degos Disease | Menkes Disease | Behavioral Variant Of Frontotemporal Dementia | Nicotine Dependence | Retinal Dystrophy | Gerstmann-Straussler-Scheinker Syndrome | Hemorrhagic Disorders | Best Macular Dystrophy | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Charcot-Marie-Tooth Disease, Type 2C | Mucolipidosis Type II | Melanocytic Nevus | Maple Syrup Urine Disease | Non-Hodgkin Lymphoma | Duchenne Muscular Dystrophy | Hypersensitivity | Anuria | Pituitary Dwarfism | Isovaleric Acidemia | Pneumonia, Bacterial | Infectious Diarrhea | Congenital Diaphragmatic Hernia | Hyperammonemia | Ganglioglioma | Creatine Deficiency Syndrome | Venous Insufficiency | Amyotrophic Lateral Sclerosis, Juvenile | Amenorrhea | Spinocerebellar Ataxia Type 16 | Bruck Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Congenital Afibrinogenemia | Orthostatic Intolerance | Nijmegen Breakage Syndrome | Bare Lymphocyte Syndrome | Multiple Sclerosis, Relapsing-remitting | Methemoglobinemia | Trichorhinophalangeal Syndrome | Autonomic Nervous System Disorders | Gardner Syndrome | IMAGe Syndrome | Hereditary Xerocytosis | Osmotic Demyelination Syndrome | Postaxial Polydactyly | Thromboembolism | Episodic Ataxia | Renal Failure | Hydrocephalus | Glycogen Storage Disease | Keratocystic Odontogenic Tumor | Tendinitis | B-cell Chronic Lymphocytic Leukemia | Histiocytosis | Colorectal Adenoma | Sarcoma | AIDS | Birk-Barel Syndrome | Dysfibrinogenemia | Progressive Familial Intrahepatic Cholestasis Type 3 | Dental Caries | PHARC Syndrome | Glaucoma, Congenital | Pernicious Anemia | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Malnutrition | Chanarin-Dorfman Syndrome | Calcium Pyrophosphate Deposition Disease | Premenstrual Syndrome | Kabuki Syndrome | Presbycusis | Polycystic Kidney, Autosomal Recessive | Familial Mediterranean Fever | Esthesioneuroblastoma | Lissencephaly 2 | Heart Block | Multiple Sclerosis, Chronic Progressive | Rhabdomyosarcoma, Embryonal | Dentinogenesis Imperfecta | Lymphedema | Lennox-Gastaut Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Aldosterone Synthase Deficiency | Tic Disorder | Exostoses | Skin Carcinoma | Growth Hormone Excess | Neuropathy | Congenital Hereditary Endothelial Dystrophy Type II | Jaundice, Obstructive | Arteriosclerosis | Japanese Encephalitis | Wolman Disease | Angiomyolipoma | Saethre-Chotzen Syndrome | HUPRA Syndrome | Adrenal Insufficiency | Incontinentia Pigmenti | Lyme Disease | Leishmaniasis, Cutaneous | Neurodermatitis | Polyarteritis Nodosa | Orotic Aciduria | Pleural Tuberculosis | Charcot-Marie-Tooth Disease Type 2E | Prolactinoma | Nestor-Guillermo Progeria Syndrome | Alazami Syndrome | Sarcoma, Ewing | CDKL5 Deficiency Disorder | Dyslipidemia | Chronic Enteropathy Associated With SLCO2A1 Gene | Roberts Syndrome | Primary Pigmented Nodular Adrenocortical Disease | FG Syndrome | Methylmalonic Acidemia | Aplasia Cutis Congenita | Benign Familial Neonatal Convulsions | Molybdenum Cofactor Deficiency | Creatine Deficiency Syndrome Due To AGAT Deficiency | Eccrine Porocarcinoma | Osteonecrosis Of The Jaw | Generalized Epilepsy With Febrile Seizures Plus | Rickets | Lysosomal Acid Lipase Deficiency | Basal Cell Nevus Syndrome | Glutaric Aciduria Type 3 | Dysequilibrium Syndrome | Toxic Epidermal Necrolysis | 3-methylglutaconic Aciduria | Prune Belly Syndrome | High Molecular Weight Kininogen Deficiency | Cholelithiasis | Subacute Sclerosing Panencephalitis | Palmoplantar Keratoderma | Pulmonary Tuberculosis | Monilethrix | Pelizaeus-Merzbacher Disease | Necrotizing Autoimmune Myopathy | Papilledema | Retinitis | Acute Myeloid Leukemia | Hereditary Neuropathy With Liability To Pressure Palsies | Angina Pectoris | Enhanced S-cone Syndrome | Familial Isolated Hyperparathyroidism | Myelofibrosis | Conjunctivitis, Allergic | Spondyloarthritis | Peters-plus Syndrome | Hypokalemia | Xeroderma Pigmentosum | Leukodystrophies | Marfan Syndrome | Congestive Heart Failure | Cornelia De Lange Syndrome | Schizotypal Personality Disorder | Hypothalamic Obesity | Silicosis | Gangliosidosis | Ureteropelvic Junction Obstruction | Schwannoma | Richter's Syndrome | Cutaneous Lupus Erythematosus | Hyperinsulinism-hyperammonemia Syndrome | Ornithine Transcarbamylase Deficiency | Niemann-Pick Disease, Type A | Pontocerebellar Hypoplasia Type 2