Disease

PASLI Disease

About the Disease
Immunodeficiency 14, also known as activated pi3k-delta syndrome, is related to immunodeficiency 14a, autosomal dominant and agammaglobulinemia, x-linked. An important gene associated with Immunodeficiency 14 is PIK3CD (Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Delta), and among its related pathways/superpathways are Innate Immune System and Signal Transduction. The drugs Miconazole and Sirolimus have been mentioned in the context of this disorder. Affiliated tissues include t cells, b cells and prefrontal cortex, and related phenotypes are Decreased viability and Decreased viability

Common Targets
PIK3CD | PIK3R1

疾病靶点研报
PASLI Disease

Note: If you'd like to get a target analysis report for PASLI Disease, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of PASLI Disease at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Cerebellofaciodental Syndrome | Alexander Disease | Urolithiasis | Hypotension, Orthostatic | Diabetic Nephropathy | Viral Meningitis | Joubert Syndrome | Pyruvate Decarboxylase Deficiency | Choroideremia | Roberts Syndrome | Leishmaniasis, Visceral | Lymphedema-distichiasis Syndrome | Hypercalciuria | Compartment Syndrome | Carotid Artery Disease | Lattice Corneal Dystrophy Type 1 | HANAC Syndrome | Congenital Absence Of Vas Deferens | Pituitary Stalk Interruption Syndrome | Malignant Fibrous Histiocytoma | Acute Coronary Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Liddle Syndrome | Hyperammonemia | Malaria, Cerebral | Inflammatory Myopathy | Endophthalmitis | Gerodermia Osteodysplastica | Chondrodysplasia Punctata | Rett Syndrome | Basan Syndrome | Spinocerebellar Ataxia Type 27 | Rhabdomyosarcoma, Alveolar | Occipital Neuralgia | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Congenital Fiber-type Disproportion Myopathy | Wolfram Syndrome 2 | Tyrosine Hydroxylase Deficiency | Lentigo | Glycogen Storage Disease | Mycosis Fungoides | Hypereosinophilic Syndrome | Perry Syndrome | Motion Sickness | Primary Pigmented Nodular Adrenocortical Disease | Schamberg Disease | Transient Bullous Dermolysis Of The Newborn | Lymphomatoid Granulomatosis | Alstrom Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Pouchitis | Lymphoma Lymphoblastic | Basal Ganglia Cerebrovascular Disease | Jalili Syndrome | Porencephaly | Hepatic Veno-occlusive Disease | Smith-Kingsmore Syndrome | Hepatoblastoma | Spinocerebellar Ataxia Type 21 | Glomerulonephritis, Membranous | Cyst | Sensorineural Hearing Loss | Spina Bifida | Intellectual Disability, Autosomal Dominant 5 | Lymphoma, Follicular | Short-chain Acyl-CoA Dehydrogenase Deficiency | Borjeson-Forssman-Lehmann Syndrome | Palmoplantar Keratoderma | Anovulation | Agammaglobulinemia | Chronic Granulomatous Disease | Autosomal Recessive Congenital Ichthyosis | Mucolipidosis Type IV | Scoliosis | Hypertension, Essential | Dupuytren Disease | Filariasis | 3-hydroxy-3-methylglutaric Aciduria | Sick Sinus Syndrome 1 | Neurotoxicity | LMNA-related Congenital Muscular Dystrophy | Neurofibromatosis-Noonan Syndrome | Mucolipidosis | Hereditary Folate Malabsorption | Torticollis | Otopalatodigital Syndrome Type 2 | Epilepsy Of Infancy With Migrating Focal Seizures | Papulopustular Rosacea | Iron Deficiency Anemia | Cancer, Kidney | Measles | Sarcoma, Endometrial Stromal | Photosensitivity | Schwannomatosis | Enterocolitis, Necrotizing | Pseudohypoparathyroidism Type 1C | Hairy Cell Leukemia | Oral Lichen Planus | Treacher Collins Syndrome | Spermatocele | Ventricular Septal Defect | Renpenning Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Pachyonychia Congenita | Vertigo | Macrophagic Myofasciitis | Lymphoma, Mantle Cell | Bursitis | Thyroid Hormone Resistance | Dysmorphophobia | Proteasome-associated Autoinflammatory Syndrome 2 | Glycogen Storage Disease Type 3 | Astrocytoma, Anaplastic | Benign Familial Pemphigus | Canavan Disease | Genee-Wiedemann Syndrome | Charcot-Marie-Tooth Disease Type 3 | Polycystic Kidney, Autosomal Dominant | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Jawad Syndrome | Pneumococcal Meningitis | Cancer, Prostate | Chronic Myeloid Leukemia | Focal Segmental Glomerulosclerosis | Withdrawal Syndrome | Polymyalgia Rheumatica | Antiphospholipid Syndrome | Zygomycosis | Antenatal Bartter Syndrome Type 1 | Glycogen Storage Disease Type 4 | Skin Papilloma | Antisocial Personality Disorder | Pycnodysostosis | Spinocerebellar Ataxia Type 10 | Lipid Metabolism Disorders | Craniopharyngioma | Chronic Thromboembolic Pulmonary Hypertension | Anorchia | Benign Recurrent Intrahepatic Cholestasis 1 | Cushing Syndrome | Acute Motor Axonal Neuropathy | Vitamin B12 Deficiency | Renal Failure | Uveitis | Haim-Munk Syndrome | Personality Disorders | Polymicrogyria | Carcinoma, Transitional Cell | Benign Familial Infantile Seizures | Agnathia-Otocephaly Complex | Toxic Epidermal Necrolysis | Loeys-Dietz Syndrome Type 4 | MIRAGE Syndrome | Scleroderma | Tangier Disease | Adenosine Deaminase Deficiency | Epidermodysplasia Verruciformis | Maternally Inherited Diabetes And Deafness | Cystinuria | Vulvovaginitis | Thanatophoric Dysplasia Type 1 | Primary Familial Brain Calcification | Microphthalmia, Syndromic 7 | McKusick Type Metaphyseal Chondrodysplasia | Polycystic Ovary Syndrome | Ocular Albinism Type 1 | Multiple Sclerosis, Chronic Progressive | Hypohidrotic Ectodermal Dysplasia, X-linked | Basal Ganglia Disease, Biotin-responsive | Spinocerebellar Ataxia Type 31 | VEXAS Syndrome | Patent Ductus Arteriosus | Hereditary Mixed Polyposis Syndrome | Adenoid Cystic Carcinoma | Hyperlipidemia | Exocrine Pancreatic Insufficiency | Loeys-Dietz Syndrome | Relapsing Polychondritis | Muscle Wasting | Sclerocornea | Ehlers-Danlos Syndrome | Micro Syndrome | Cornelia De Lange Syndrome | Hidradenitis | Isovaleric Acidemia | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Conjunctivitis, Allergic | Syphilis | Pseudohypoaldosteronism | Dystrophy, Cone-rod | Dysequilibrium Syndrome | Intracerebral Hemorrhage | Myocarditis | Lymphopenia | Beta-Propeller Protein-associated Neurodegeneration | Mitochondrial Encephalomyopathy | Cockayne Syndrome | Heimler Syndrome | NGLY1 Deficiency | Spinocerebellar Ataxia Type 14 | Carpal Tunnel Syndrome | Synpolydactyly | Warsaw Breakage Syndrome | Coronary Artery Disease | Alopecia Totalis | Giant Cell Arteritis | Cardiomyopathy, Restrictive | Cyclic Vomiting Syndrome | Carcinoma In Situ | Encephalopathy, Glycine | Smith-Magenis Syndrome | Sensory Neuropathy | Multifocal Motor Neuropathy | Tracheal Disorders | Corneal Dystrophy And Perceptive Deafness | Cardiomyopathy, Hypertrophic | X-linked Acrogigantism | Pseudohypoparathyroidism Type 2 | Splenomegaly | Nanophthalmos | Aldosteronism | Hypotrichosis | Corneal Ulcer | Vestibular Disease | Apraxia | Familial Hypobetalipoproteinemia | Methemoglobinemia Type IV | Maple Syrup Urine Disease | Myasthenia Gravis | Myopathy | Charcot-Marie-Tooth Disease, Type 6 | Familial Advanced Sleep Phase Syndrome | Extramammary Paget's Disease | Cranioectodermal Dysplasia | Beare-Stevenson Syndrome | Herpes Genitalis | Early Infantile Epileptic Encephalopathy 4 | DNA Ligase IV Deficiency | Anxiety Disorders | Diabetes Insipidus | Thyroiditis, Autoimmune | Japanese Encephalitis | Blue Rubber Bleb Nevus Syndrome | Mabry Syndrome | Meningioma | Evans Syndrome | Corneal Edema | Spinal Muscular Atrophy Type 2 | Ulcerative Colitis | Pure Autonomic Failure | Bronchiolitis | Congenital Disorders Of Glycosylation | Platelet Disorders | Diabetes | Nephrocalcinosis | Chromosome 9q34.3 Deletion Syndrome | Stroke, Hemorrhagic | Peritonitis | Farber Disease | Presbyopia | Isobutyryl-CoA Dehydrogenase Deficiency | Superficial Spreading Melanoma | Acrodermatitis | Spinocerebellar Ataxia Type 42 | Galactosialidosis | Cocaine-Related Disorders | Charcot-Marie-Tooth Disease Type 4E | Melanoma, Uveal | Angina Pectoris | Avian Influenza | Goiter | Vici Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | Gastritis | Ameloblastoma | Macular Corneal Dystrophy Type 1 | Neurocutaneous Syndromes | Hypertension, Portal | Spinocerebellar Ataxia Type 2 | Familial Male-limited Precocious Puberty | Autoimmune Polyendocrine Syndrome | Chronic Neutrophilic Leukemia | Opisthorchiasis | Teratozoospermia | Cold Agglutinin Disease | Rift Valley Fever | Stargardt Disease | Cholangiocarcinoma | Bartsocas-Papas Syndrome | Waardenburg Syndrome Type 4 | Schizophrenia | Lennox-Gastaut Syndrome | Bietti Crystalline Dystrophy | Congenital Muscular Dystrophy | Metabolic Syndrome | Schizophrenia, Paranoid | Kabuki Syndrome | Schwartz-Jampel-Aberfeld Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | CHOPS Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Anodontia | Congenital Dysfibrinogenemia | Mumps | Bruck Syndrome | Intestinal Pseudo-obstruction | Epilepsy | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Rheumatoid Arthritis | Mevalonate Kinase Deficiency | Nephropathy | Retinopathy Of Prematurity | Dyggve-Melchior-Clausen Disease | Hypokalemia | Angiodysplasia | Niemann-Pick Disease, Type C | Low Phospholipid Associated Cholelithiasis | Polyneuropathy | Kashin-Beck Disease | Blepharophimosis Syndrome | Episodic Ataxia | Small Lymphocytic Lymphoma | Impetigo | Familial Glucocorticoid Deficiency | Alkaptonuria | Macular Degeneration | Bone Marrow Necrosis | Paroxysmal Nocturnal Hemoglobinuria | Potocki-Shaffer Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Hemoglobinopathies | Gout | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Craniometaphyseal Dysplasia | Dwarfism | Huntington's Disease | Anuria | Pernicious Anemia | Neuroectodermal Tumors, Primitive | Cole-Carpenter Syndrome | Histoplasmosis | Alcoholism | ACTH-independent Macronodular Adrenal Hyperplasia | Aneurysm, Thoracic Aortic | Gardner Syndrome | Trachoma | Bronchitis | Polyarteritis Nodosa | Melanoma, Malignant | Hypotonia-cystinuria Syndrome | Hepatitis B, Chronic | Wolfram Syndrome | Histiocytic Sarcoma | Monilethrix | Motor Neuron Diseases | Steel Syndrome | Pemphigus Vulgaris | Sarcoma | Cerebellar Ataxia, Cayman Type | Retinal Dystrophy, Early-onset Severe | Heroin Dependence | Necrobiosis Lipoidica | Adrenoleukodystrophy, X-linked | Ophthalmia, Sympathetic | Exfoliative Dermatitis | Multiple Sclerosis | Smoldering Myeloma | Gnathodiaphyseal Dysplasia | Carcinoma, Signet Ring Cell | Osteoarthritis | Periventricular Leukomalacia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Ectodermal Dysplasia | Scapuloperoneal Spinal Muscular Atrophy | Esophagitis, Eosinophilic | Myoclonus-dystonia Syndrome | Emery-Dreifuss Muscular Dystrophy | Congenital Myopathy | Acute Leukemia | Acrodermatitis Enteropathica | Epidermal Nevus Syndrome | Bladder Exstrophy | Bare Lymphocyte Syndrome | Spinocerebellar Ataxia Type 1 | Metaphyseal Chondrodysplasia, Schmid Type | Leri Pleonosteosis | Persistent Mullerian Duct Syndrome | Primary Cutaneous Amyloidosis | Persistent Fetal Circulation | Blepharoconjunctivitis | Myotonia | Encephalopathy, Hepatic | Infertility | Congenital Torticollis | Hypopigmentation | Sulfite Oxidase Deficiency | DiGeorge Syndrome | Ameloblastic Carcinoma | Stiff-man Syndrome