LRBA Deficiency

About the Disease
Lrba Deficiency is related to immunodeficiency, common variable, 8, with autoimmunity and immune deficiency disease. The drugs Abatacept and Antirheumatic Agents have been mentioned in the context of this disorder. Affiliated tissues include b cells, t cells and bone marrow.

Common Targets
LRBA

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Other Diseases

Motion Sickness | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Wolcott-Rallison Syndrome | Hypopigmentation | Split Hand-foot Malformation | Twin-to-twin Transfusion Syndrome | Liddle Syndrome | Combined Pituitary Hormone Deficiency | Fraser Syndrome | Basal Ganglia Cerebrovascular Disease | AIDS Dementia Complex | Hemorrhagic Disorders | Leukoplakia, Oral | Branchiootorenal Syndrome | Gangliosidosis | Majeed Syndrome | Histiocytic Sarcoma | Erysipelas | Cardiomyopathy, Peripartum | Porphyria, Acute Intermittent | Best Macular Dystrophy | Spinocerebellar Ataxia Type 23 | Pitt-Hopkins Syndrome | Marfan Syndrome | Cluster Headache | NGLY1 Deficiency | Hepatitis A | Pulverulent Zonular Cataract | Tyrosinemia | Spastic Paraplegia Type 7 | Agoraphobia | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Hypertrophy | X-linked Sideroblastic Anemia | Trismus-pseudocamptodactyly Syndrome | Erectile Dysfunction | Spinal Muscular Atrophy Type 2 | Hyperparathyroidism-jaw Tumor Syndrome | Vitamin A Deficiency | Osteochondroma | Coronary Restenosis | Pneumonia, Bacterial | Palsy, Cerebral | Bartsocas-Papas Syndrome | Inborn Errors Of Metabolism | Carotid Artery Disease | Central Retinal Artery Occlusion | VACTERL/VATER Association | Hoyeraal-Hreidarsson Syndrome | Molybdenum Cofactor Deficiency | Carbohydrate Metabolism Disorders | Keratosis, Actinic | Farber Disease | Enhanced S-cone Syndrome | Autonomic Neuropathy | Oligodendroglioma | Wolff-Parkinson-White Syndrome | Small Lymphocytic Lymphoma | Inflammatory Myopathy | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Creutzfeldt-Jakob Disease | Glycogen Storage Disease Type 0, Muscle | Cholelithiasis | Hypoplastic Left Heart Syndrome | Polycystic Liver | Long QT Syndrome Type 2 | Blastomycosis | Gitelman Syndrome | Charcot-Marie-Tooth Disease Type 4B1 | Melanoma, Uveal | DRESS Syndrome | Rothmund-Thomson Syndrome | Spinocerebellar Ataxia Type 40 | Lathosterolosis | Tetraplegia | Osteomyelitis | Shock, Cardiogenic | Hypopituitarism | Presbycusis | Retinal Telangiectasia | Leukemia | Fibrodysplasia Ossificans Progressiva | Meningioma | Dysequilibrium Syndrome | Cousin Syndrome | Metachromatic Leukodystrophy | Nutrition Disorders | Anorectal Malformations | Non-bullous Congenital Ichthyosiform Erythroderma | Hepatitis, Autoimmune | Acute Kidney Injury | Liver Failure, Acute Infantile | Beckwith-Wiedemann Syndrome | Macrophagic Myofasciitis | Encephalopathy, Glycine | Thrombophilia | Hepatorenal Syndrome | Skin Papilloma | Krabbe Disease | Lennox-Gastaut Syndrome | Photosensitivity | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Cerebrotendinous Xanthomatosis | Epidermolysis Bullosa Simplex, Generalized | Non-proliferative Diabetic Retinopathy | Cerebral Cavernous Malformations | Optic Atrophy 2 | Bacterial Meningitis | Acute Leukemia | Abetalipoproteinemia | Non-Langerhans Cell Histiocytosis | Congenital Hemolytic Anemia | Poretti-Boltshauser Syndrome | Osteonecrosis | Cutaneous T-cell Lymphoma | Multiple Sclerosis, Primary Progressive | Mastitis | Pyloric Stenosis, Infantile Hypertrophic | Schuurs-Hoeijmakers Syndrome | Hypereosinophilic Syndrome | Malignant Fibrous Histiocytoma | Erythromelalgia | Pelvic Inflammatory Disease | Birt-Hogg-Dube Syndrome | Hyperparathyroidism | DNA Ligase IV Deficiency | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Superficial Spreading Melanoma | Fibromuscular Dysplasia | Acute Motor Axonal Neuropathy | Epidermolysis Bullosa Simplex, Localized | Pre-eclampsia | Hemorrhoids | Leishmaniasis, Cutaneous | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Aldosterone Deficiency | Thin Basement Membrane Disease | Binge Eating Disorder | Hemolytic Uremic Syndrome, Atypical | Pancreatitis | Uremic Pruritus | Acquired Partial Lipodystrophy | Leri Pleonosteosis | Pneumothorax | Glycogen Storage Disease Type 1 | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Bipolar Disorder | Pseudohypoparathyroidism Type 2 | Osteogenesis Imperfecta | Chondrodysplasia Punctata 2, X-linked Dominant | Alazami Syndrome | Metabolic Syndrome | Interstitial Lung Diseases | Coloboma | Acrodermatitis | Spondylolisthesis | Tardive Dyskinesia | Niemann-Pick Disease, Type B | Juvenile Xanthogranuloma | Acute Lung Injury | Lipodystrophy | Atelosteogenesis Type 1 | Spasticity | Emery-Dreifuss Muscular Dystrophy | Usher Syndrome | Adenylosuccinate Lyase Deficiency | Endophthalmitis | Primary Hyperoxaluria Type 1 | Ichthyosis Bullosa Of Siemens | Hereditary Inclusion Body Myopathy | Xeroderma Pigmentosum Variant Type | Myotonic Disorders | Mohr-Tranebjaerg Syndrome | Hereditary Spastic Paraplegia | Malaria | Endometritis | Bardet-Biedl Syndrome | Christianson Syndrome | Hernia, Inguinal | Dysfibrinogenemia | Prolymphocytic Leukemia | Spinocerebellar Ataxia | Amyloidosis | Primary Carnitine Deficiency | Antley-Bixler Syndrome | Congenital Disorders Of Glycosylation Type II | REM Sleep Behavior Disorder | Myelodysplasia | Hartnup Disease | Absence Epilepsy | Charcot-Marie-Tooth Disease, Type 6 | Sarcomatoid Carcinoma Of The Lung | Joubert Syndrome | Gynecomastia | Epidermolytic Hyperkeratosis | Fundus Albipunctatus | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Herpes Genitalis | Takotsubo Cardiomyopathy | Coenzyme Q10 Deficiency | Scleroderma | Veno-occlusive Disease | Hypertriglyceridemia | Colitis | Gingivitis | Myoclonic Atonic Epilepsy | Kindler Syndrome | Spinocerebellar Ataxia Type 2 | Acute Generalized Exanthematous Pustulosis | Schizotypal Personality Disorder | Campomelic Dysplasia | Waardenburg Syndrome Type 4 | Acute Anterior Uveitis | Mumps | Neurogenic Bladder | Retinal Detachment | Progressive Familial Intrahepatic Cholestasis Type 1 | Sengers Syndrome | Vitamin K Deficiency | Endometriosis | Cholecystitis | Lymphoma, AIDS-related | Sjogren Syndrome | Fanconi Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Hypothalamic Obesity | Hypersensitivity Pneumonitis | Uterine Leiomyoma | Schindler Disease | Proteus Syndrome | Wolman Disease | Waardenburg Syndrome Type 2A | Tatton-Brown-Rahman Syndrome | Hypermethioninemia | Micro Syndrome | GM2-gangliosidosis AB Variant | High Molecular Weight Kininogen Deficiency | Chronic Kidney Disease | Erythrokeratodermia Variabilis | Anencephaly | Kawasaki Disease | Dominant Optic Atrophy | Liver Failure | Lipid Storage Myopathy | Carbonic Anhydrase VA Deficiency | Sotos Syndrome | Erythema Nodosum | Fatty Aldehyde Dehydrogenase Deficiency | Gestational Trophoblastic Disease | PASLI Disease | Syndactyly | Dementia | Sleep Apnea | Alpers Syndrome | Cataplexy | Protein C Deficiency | Diabetes Gestational | Glioblastoma Multiforme | Sarcoma, Endometrial Stromal | Dysgerminoma | Diarrhea | Hemangioma | Early Infantile Epileptic Encephalopathy 4 | Multiple Myeloma | Urticaria | Primary Familial Brain Calcification | Scapuloperoneal Spinal Muscular Atrophy | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Tetanus | Osteoporosis-pseudoglioma Syndrome | Osteogenesis Imperfecta Type VI | X-linked Myotubular Myopathy | Lymphangiomatosis | Alzheimer Disease, Late Onset | Congenital Tufting Enteropathy | Otopalatodigital Syndrome Type 2 | Extramammary Paget's Disease | Hypermetropia | Colitis, Microscopic | Ectrodactyly | Lateral Meningocele Syndrome | Multiple Sclerosis | Dermatofibrosarcoma | HIBCH Deficiency | Spinocerebellar Ataxia Type 27 | Orotic Aciduria | Basal Cell Nevus Syndrome | Acne | Peripheral Neuropathy | Chondroma | Pancreatitis, Chronic | Esotropia | Parkinson's Disease | Neurofibromatosis-Noonan Syndrome | Prostatitis | Sturge-Weber Syndrome | Hyperglycemia | Graves Disease | Autoimmune Disease | Pituitary Disorders | Osteogenesis Imperfecta Type II | Keratosis, Seborrheic | Adult Polyglucosan Body Disease | LEOPARD Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Liebenberg Syndrome | Mitochondrial Encephalomyopathy | Non-epidermolytic Palmoplantar Keratoderma | Cystitis | Lymphopenia | Dupuytren Disease | Myopathy | Plasma Cell Dyscrasia | Gyrate Atrophy Of The Choroid And Retina | Familial Exudative Vitreoretinopathy | Alexander Disease | Nestor-Guillermo Progeria Syndrome | Norrie Disease | Sarcoma | Urethritis | Dysplastic Nevus | Chronic Inflammatory Demyelinating Polyneuropathy | Eclampsia | Syphilis | Polymyositis | Nevus | Epidermal Nevus Syndrome | Alpha-1 Antitrypsin Deficiency | Porphyria | Oral Lichen Planus | Echinococcosis | Adams-Oliver Syndrome | Hemangioendothelioma | Progressive Myoclonic Epilepsy | Encephalitis, Tick-borne | Silicosis | Malaria, Cerebral | Bone Giant Cell Tumor | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Paroxysmal Kinesigenic Dyskinesia | Hepatopulmonary Syndrome | Primary Sclerosing Cholangitis | Williams Syndrome | Essential Fructosuria | Hyperekplexia | Autoimmune Autonomic Ganglionopathy | Dementia, Vascular | COACH Syndrome | Kohlschutter-Tonz Syndrome | Multiple Sclerosis, Chronic Progressive | Polydactyly | Keratopathy | Jalili Syndrome | Pseudomyxoma Peritonei | Temporal Lobe Epilepsy | Bladder Exstrophy | Onchocerciasis | Sarcoma, Alveolar Soft Part | Spinal Muscular Atrophy Type 3 | Inflammatory Myofibroblastic Tumor | Agranulocytosis | Lichen Sclerosus | Intermittent Explosive Disorder | Von Hippel-Lindau Disease | Sulfite Oxidase Deficiency | Malonyl-CoA Decarboxylase Deficiency | Endocarditis | Hypotrichosis Simplex | Oligospermia | Sickle Cell Anemia | Frank-ter Haar Syndrome | Cysticercosis | Blue Nevus | Pulmonary Alveolar Proteinosis | GAPO Syndrome | Gilbert Syndrome | Adrenomyeloneuropathy | Anal Fissure | Chorea | Myelitis, Transverse | Conn Syndrome | Cri-du-chat Syndrome | Auriculocondylar Syndrome | Huntington's Disease | Dyskeratosis Congenita | Holoprosencephaly | Argininosuccinic Aciduria | Macular Degeneration | Charcot-Marie-Tooth Disease, Type 2A | Zygomycosis | Astrocytoma, Anaplastic | Spina Bifida | Potocki-Shaffer Syndrome | Pemphigoid | Pheochromocytoma | Cutis Laxa | Anti-NMDA Receptor Encephalitis | Hypotension, Orthostatic | Microphthalmia, Syndromic 7 | Amebiasis