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 / Biomarkers
G10498 | Serine/Threonine Kinase (nonspecified subtype) | G55170 | G55869 | G8841 | G598 | P6058 | G7046 | G80862 | G3447 | G54851 | G1803 | G1020 | G6352 | G729230 | G4192 | CDK5/p25 | G1495 | G56341 | G7015 | G958 | G836 | Cyclin-dependent kinase (nonspecified subtype) | G10455 | G4313 | CDK9/Cyclin T1 | G1025 | Protein Tyrosine Phosphatase (PTP) (nonspecified subtype) | G8856 | P16126 | G6868 | G3717 | P6348 | Mitogen-Activated Protein Kinase (nonspecified subtype) | G4170 | G54106 | Casein kinase I (nonspecified subtype) | P5698 | G5894 | G10747 | G79885 | G3458 | Histone acetyltransferase (HAT) (nonspecified subtype) | G904 | G9403 | G3558 | G7099 | P13024 | Histone deacetylase (nonspecified subtype) | G164668 | G3276 | G1234 | G10461 | G728642 | G5170 | G6387 | G404220 | G4361 | G2548 | G23028 | G2798 | G120227 | G3567 | G2538 | G11184 | G5133 | G2990 | Interferon alpha/beta Receptor (nonspecified subtype) | G920 | G3565 | P11025 | CDK1/Cyclin B | G94 | G1786 | G5292 | G6869 | G1994 | G6992 | G1984 | Nitric oxide synthase (NOS) (nonspecified subtype) | G7251 | CDK2/Cyclin A | G1725 | G6646 | Sterol O-acyltransferase (ACAT) (nonspecified subtype) | G1230 | G80352 | G3107 | G6999 | G1636 | G4907 | G7301 | G11103 | G5243 | G51284 | G8737 | G115650 | G983 | G10013 | G1555 | G1956 | G1269 | Cyclin A (nonspecified subtype) | G3454 | Rho kinase (ROCK) (nonspecified subtype) | G27113 | G3066 | G595 | G5422 | G7124 | Cyclin-dependent kinase inhibitor (nonspecified subtype) | G3106 | G60489 | G3620 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | G5868 | Phosphodiesterase (nonspecified subtype) | G8435 | G1017 | G341392 | P8262 | G1019 | G3569 | G5743 | G29110 | G3455 | G1594 | G1021 | P6884 | G5423 | G64115 | G1557 | G6401 | G9641 | G3065 | G5742 | G10196 | G23476 | G105375015 | G5142 | G5150 | G5873 | Transforming growth factor (TGF)-beta receptor (nonspecified subtype) | G1232 | G11040 | Cyclin B (nonspecified subtype) | G7852 | G9034 | G30834 | G1440 | G558 | G10320 | G5771 | Lipoxygenase (nonspecified subtype) | G5875 | G134 | G3586 | G197259 | Ribonucleoside-diphosphate reductase | DNA Topoisomerase II (nonspecified subtype)
Other Diseases
AIDS Dementia Complex | Alagille Syndrome | Alazami Syndrome | Albinism | Alcoholism | Aldosterone Deficiency | Aldosterone Synthase Deficiency | Aldosteronism | Alexander Disease | Allan-Herndon-Dudley Syndrome | Allergic Contact Dermatitis | Alopecia | Alopecia Areata | Alopecia Totalis | Alpers Syndrome | Alpha-1 Antitrypsin Deficiency | Alpha-mannosidosis | Alpha-thalassemia Myelodysplasia Syndrome | Alstrom Syndrome | Alveolar Capillary Dysplasia | Alzheimer Disease, Late Onset | Amblyopia | Amelanotic Melanoma | Ameloblastic Carcinoma | Ameloblastoma | Amelogenesis Imperfecta | Amenorrhea | Amish Infantile Epilepsy Syndrome | Amyloidosis | Amyotrophic Lateral Sclerosis | Amyotrophic Lateral Sclerosis, Juvenile | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Anal Fissure | Analgesia | Androgenic Alopecia | Anemia | Anencephaly | Aneurysm, Abdominal Aortic | Aneurysm, Thoracic Aortic | Angelman Syndrome | Angina Pectoris | Angiodysplasia | Angioedema | Angioedema, Acquired | Angioedema, Hereditary | Angioimmunoblastic T-cell Lymphoma | Angiomyolipoma | Angiosarcoma | Angiosarcoma Of The Breast | Anodontia | Anorchia | Anorectal Fistula | Anorectal Malformations | Anorexia Nervosa | Anosmia, Congenital | Anovulation | Antenatal Bartter Syndrome Type 1 | Anterior Segment Dysgenesis | Anthrax | Anti-glomerular Basement Membrane Disease | Anti-NMDA Receptor Encephalitis | Antiphospholipid Syndrome | Antisocial Personality Disorder | Antisynthetase Syndrome | Antithrombin III Deficiency | Antley-Bixler Syndrome | Anuria | Anxiety Disorders | Apert Syndrome | Aphasia | Aplasia Cutis Congenita | Aplastic Anemia | Apparent Mineralocorticoid Excess Syndrome | Apraxia | Arrhythmogenic Right Ventricular Cardiomyopathy | Arterial Tortuosity Syndrome | Arteriosclerosis | Arteriovenous Malformations | Arthritis | Arthritis, Gouty | Arthritis, Psoriatic | Arthritis, Reactive | Arthrogryposis | Arthropathy | Arts Syndrome | Aspartylglycosaminuria | Asperger Syndrome | Aspergillosis | Asphyxia Neonatorum | Asplenia | Asthma | Asthma, Exercise-induced | Asthma, Nocturnal | Astigmatism | Astrocytoma | Astrocytoma, Anaplastic | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Ataxia-ocular Apraxia 2 | Atelosteogenesis Type 1 | Atelosteogenesis Type 2 | Atherosclerosis | Atopic Dermatitis | Atopy | Atrial Septal Defect | Atrioventricular Septal Defect | Auriculocondylar Syndrome | Autism | Autism Spectrum Disorders | Autoimmune Autonomic Ganglionopathy | Autoimmune Disease | Autoimmune Hemolytic Anemia | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Autoimmune Polyendocrine Syndrome | Autonomic Nervous System Disorders | Autonomic Neuropathy | Autosomal Recessive Bestrophinopathy | Autosomal Recessive Congenital Ichthyosis | Autosomal Recessive Spastic Paraplegia Type 35 | Autosomal Recessive Spastic Paraplegia Type 54 | Avellino Corneal Dystrophy | Axenfeld-Rieger Syndrome | Azoospermia | B-cell Chronic Lymphocytic Leukemia | B-cell Prolymphocytic Leukemia | Babesiosis | Bacterial Meningitis | Bainbridge-Ropers Syndrome | Barakat Syndrome | Bardet-Biedl Syndrome | Bare Lymphocyte Syndrome | Barrett Esophagus | Bartsocas-Papas Syndrome | Bartter Syndrome | Basal Cell Nevus Syndrome | Basal Ganglia Cerebrovascular Disease | Basal Ganglia Disease | Basal Ganglia Disease, Biotin-responsive | Basan Syndrome | Batten Disease | Beare-Stevenson Syndrome | Becker Muscular Dystrophy | Beckwith-Wiedemann Syndrome | Behavioral Variant Of Frontotemporal Dementia | Behcet's Disease | Benign Familial Infantile Seizures | Benign Familial Neonatal Convulsions | Benign Familial Pemphigus | Benign Hereditary Chorea | Benign Recurrent Intrahepatic Cholestasis 1 | Bernard-Soulier Syndrome | Best Macular Dystrophy | Beta-Propeller Protein-associated Neurodegeneration | Bethlem Myopathy | Bicuspid Aortic Valve | Bietti Crystalline Dystrophy | Binge Eating Disorder | Biotinidase Deficiency | Bipolar Disorder | Birk-Barel Syndrome | Birt-Hogg-Dube Syndrome | Bladder Exstrophy | Blastoma, Pleuropulmonary | Blastomycosis | Blau Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Blepharitis | Blepharo-cheilo-odontic Syndrome | Blepharoconjunctivitis | Blepharospasm | Blomstrand Osteochondrodysplasia | Blood Protein Disorders | Bloom Syndrome | Blue Nevus | Blue Rubber Bleb Nevus Syndrome | Bone Giant Cell Tumor | Bone Marrow Necrosis | Borderline Personality Disorder | Borjeson-Forssman-Lehmann Syndrome | Botulism | Brachial Plexus Neuropathy | Brachydactyly | Branchiootorenal Syndrome | Brenner Tumor | Bronchiectasis | Bronchiolitis | Bronchitis | Bronchitis, Chronic | Brooke-Spiegler Syndrome | Bruck Syndrome | Brugada Syndrome 1 | Budd-Chiari Syndrome | Bullous Pemphigoid | Burn-McKeown Syndrome | Bursitis | C3 Glomerulonephritis | C3 Glomerulopathy | Cabezas Syndrome | Calcium Pyrophosphate Deposition Disease | Campomelic Dysplasia | Camptocormia | Camurati-Engelmann Disease | Canavan Disease | Cancer, Bladder | Cancer, Brain | Cancer, Breast | Cancer, Colon | Cancer, Kidney | Cancer, Lung | Cancer, Prostate | Cancer, Skin | Cantu Syndrome | Carbohydrate Metabolism Disorders | Carbonic Anhydrase VA Deficiency | Carcinoid Syndrome | Carcinoid Tumor | Carcinoma In Situ | Carcinoma, Merkel Cell | Carcinoma, Signet Ring Cell | Carcinoma, Small Cell | Carcinoma, Squamous Cell | Carcinoma, Transitional Cell | Cardiac Arrest | Cardiac Sarcoidosis | Cardiofaciocutaneous Syndrome | Cardiomyopathy, Dilated, 1L | Cardiomyopathy, Hypertrophic | Cardiomyopathy, Restrictive | Cardiospondylocarpofacial Syndrome | Carey-Fineman-Ziter Syndrome | Carney Triad | Carney-Stratakis Syndrome | Carotid Artery Disease | Carpal Tunnel Syndrome | Cartilage Disorders | Castleman Disease | Cat Eye Syndrome | Cataplexy | Cataract | Cavitary Optic Disc Anomalies | CDKL5 Deficiency Disorder | CEDNIK Syndrome | Celiac Disease | Cellulitis | Cenani-Lenz Syndactyly Syndrome | Central Core Disease | Central Pain Syndrome | Central Retinal Artery Occlusion | Centronuclear Myopathy | Cerebellar Ataxia, Cayman Type | Cerebellofaciodental Syndrome | Cerebral Amyloid Angiopathy | Cerebral Cavernous Malformations | Cerebrotendinous Xanthomatosis | Cerebrovascular Disorders | Cervical Dystonia | Cervicitis | Chanarin-Dorfman Syndrome | Charcot-Marie-Tooth Disease | Charcot-Marie-Tooth Disease Axonal Type 2N | Charcot-Marie-Tooth Disease Type 2D | Charcot-Marie-Tooth Disease Type 2E | Charcot-Marie-Tooth Disease Type 2T | Charcot-Marie-Tooth Disease Type 3 | Charcot-Marie-Tooth Disease Type 4 | Charcot-Marie-Tooth Disease Type 4B1 | Charcot-Marie-Tooth Disease Type 4D | Charcot-Marie-Tooth Disease Type 4E | Charcot-Marie-Tooth Disease, Type 1A | Charcot-Marie-Tooth Disease, Type 2 | Charcot-Marie-Tooth Disease, Type 2A | Charcot-Marie-Tooth Disease, Type 2C | CHARGE Syndrome | Cheilitis | Chitayat Syndrome | Chloridorrhea, Congenital | Cholangiocarcinoma | Cholangitis | Cholecystitis | Cholelithiasis | Cholera | Cholestasis | Cholestasis, Intrahepatic | Cholesteryl Ester Storage Disease | Chondrodysplasia Punctata | Chondrodysplasia Punctata 1, X-linked Recessive | Chondrodysplasia Punctata 2, X-linked Dominant | Chondroma | Chondromyxoid Fibroma | Chondrosarcoma | CHOPS Syndrome | Chordoid Glioma | Chordoma | Chorea | Chorea-acanthocytosis | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Choriocarcinoma | Chorioretinitis | Choroideremia | Choroiditis | Christianson Syndrome | Chromosome 16p11.2 Deletion Syndrome | Chromosome 17q21.31 Deletion Syndrome | Chromosome 5q Deletion Syndrome | Chromosome 8q21.11 Deletion Syndrome | Chromosome 9q34.3 Deletion Syndrome | Chronic Beryllium Disease | Chronic Enteropathy Associated With SLCO2A1 Gene | Chronic Granulomatous Disease | Chronic Granulomatous Disease, X-linked | Chronic Idiopathic Myelofibrosis | Chronic Inflammatory Demyelinating Polyneuropathy | Chronic Kidney Disease | Chronic Leukemia | Chronic Lymphocytic Leukemia | Chronic Mucocutaneous Candidiasis | Chronic Myeloid Leukemia | Chronic Myelomonocytic Leukemia | Chronic Neutrophilic Leukemia | Chronic Periodontitis | Chronic Thromboembolic Pulmonary Hypertension | Chudley-McCullough Syndrome | Chylomicron Retention Disease | Chylothorax, Congenital | Cirrhosis | Citrullinemia | Cleidocranial Dysplasia | Clouston Hidrotic Ectodermal Dysplasia | Cluster Headache | COACH Syndrome | Cockayne Syndrome | Coenzyme Q10 Deficiency | Coffin-Lowry Syndrome | Coffin-Siris Syndrome | Cohen Syndrome | Cold Agglutinin Disease | Cold-induced Sweating Syndrome | Cole-Carpenter Syndrome | Colitis | Colitis, Collagenous | Colitis, Lymphocytic | Colitis, Microscopic | Coloboma | Colon Adenoma | Colorectal Adenoma | Coma | Combined Deficiency Of Factor V And Factor VIII | Combined Malonic And Methylmalonic Acidemia | Combined Pituitary Hormone Deficiency | Common Cold | Common Variable Immunodeficiency | Communication Disorders | Compartment Syndrome | Conduct Disorder | Cone Dystrophy | Congenital Absence Of Vas Deferens | Congenital Adrenal Hyperplasia | Congenital Adrenal Hyperplasia 1 | Congenital Afibrinogenemia | Congenital Aniridia | Congenital Bilateral Absence Of Vas Deferens | Congenital Bile Acid Synthesis Defect | Congenital Central Hypoventilation Syndrome | Congenital Diaphragmatic Hernia | Congenital Disorders Of Glycosylation | Congenital Disorders Of Glycosylation Type II | Congenital Dyserythropoietic Anemia | Congenital Dyserythropoietic Anemia Type 1 | Congenital Dyserythropoietic Anemia Type 4 | Congenital Dysfibrinogenemia | Congenital Fiber-type Disproportion Myopathy | Congenital Generalized Lipodystrophy | Congenital Heart Block | Congenital Heart Defects | Congenital Hemolytic Anemia | Congenital Hereditary Endothelial Dystrophy Type II | Congenital Hypofibrinogenemia | Congenital Ichthyosiform Erythroderma | Congenital Lipoid Adrenal Hyperplasia | Congenital Mirror Movements | Congenital Muscular Dystrophy | Congenital Myasthenic Syndrome | Congenital Myopathy | Congenital Nephrotic Syndrome | Congenital Nystagmus | Congenital Poikiloderma | Congenital Primary Aphakia | Congenital Sodium Diarrhea | Congenital Stationary Night Blindness | Congenital Stromal Corneal Dystrophy | Congenital Torticollis | Congenital Tufting Enteropathy | Congestive Heart Failure | Conjunctivitis | Conjunctivitis, Allergic | Connective Tissue Disorders | Constipation | Contact Dermatitis | Corneal Dystrophies, Hereditary | Corneal Dystrophy | Corneal Dystrophy And Perceptive Deafness
