Disease

Adenosine Deaminase Deficiency

About the Disease
Adenosine Deaminase Deficiency, also known as ada deficiency, is related to severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency and severe combined immunodeficiency, x-linked. An important gene associated with Adenosine Deaminase Deficiency is ADA (Adenosine Deaminase), and among its related pathways/superpathways are Cytokine Signaling in Immune system and Metabolism of nucleotides. The drugs Busulfan and Antineoplastic Agents, Alkylating have been mentioned in the context of this disorder. Affiliated tissues include skin, lung and lymph node, and related phenotypes are failure to thrive and sinusitis

Common Targets
ADAT1 | ADA | Adenosine deaminase (nonspecified subtype) | ADA2

疾病靶点研报
Adenosine Deaminase Deficiency

Note: If you'd like to get a target analysis report for Adenosine Deaminase Deficiency, 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 Adenosine Deaminase Deficiency at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Intracranial Hypertension | Bulimia Nervosa | Spondylosis | Aldosteronism | Neonatal Progeroid Syndrome | Asplenia | Pontocerebellar Hypoplasia Type 7 | Dyggve-Melchior-Clausen Disease | Jawad Syndrome | Prediabetes | Congenital Stationary Night Blindness | Giant Cell Glioblastoma | DNA Ligase IV Deficiency | Stuve-Wiedemann Syndrome | Sepiapterin Reductase Deficiency | Odonto-onycho-dermal Dysplasia | Neurocutaneous Syndromes | Aceruloplasminemia | Huntington's Disease | Epidermal Nevus Syndrome | Cenani-Lenz Syndactyly Syndrome | Benign Familial Neonatal Convulsions | Adrenal Insufficiency | Large Granular Lymphocytic Leukemia | Diffuse Intrinsic Pontine Glioma | Amyotrophic Lateral Sclerosis, Juvenile | Pantothenate Kinase-associated Neurodegeneration | Diabetes Insipidus, Nephrogenic | Campomelic Dysplasia | Congenital Hereditary Endothelial Dystrophy Type I | Cerebellofaciodental Syndrome | Spastic Paraplegia Type 7 | Asthma, Exercise-induced | Usher Syndrome Type I | Myofibromatosis | Spondylometaphyseal Dysplasia | Neuroleptic Malignant Syndrome | Thin Basement Membrane Disease | Skin Carcinoma | Charcot-Marie-Tooth Disease Type 2D | Hypertension, Portal | Epithelial-myoepithelial Carcinoma | Tylosis With Esophageal Cancer | Vogt-Koyanagi-Harada Syndrome | Methemoglobinemia Type IV | Anuria | Uveitis, Anterior | Familial Glucocorticoid Deficiency | Spinocerebellar Ataxia Type 13 | Multiple Hamartoma Syndrome | Spinocerebellar Ataxia Type 40 | Nevus | Reflex Epilepsy | Fraser Syndrome | Parvovirus B19 Infection | Sleep Apnea, Obstructive | Cirrhosis | Oligoastrocytoma | Jaundice, Obstructive | Gerodermia Osteodysplastica | Knobloch Syndrome | Presbycusis | Neurofibromatosis Type 1 | Iron Overload | Pulmonary Tuberculosis | Low Phospholipid Associated Cholelithiasis | Thyroiditis, Autoimmune | Erectile Dysfunction | Oculocutaneous Albinism Type 2 | Rhizomelic Chondrodysplasia Punctata | Carey-Fineman-Ziter Syndrome | Lichen Planus | Charcot-Marie-Tooth Disease Type 2E | Sensory Neuropathy | HELLP Syndrome | Myositis | Diverticulitis | Precocious Puberty | MIRAGE Syndrome | Central Core Disease | Pupil Disorders | Progressive Myoclonic Epilepsy | Hypertrophy | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Autosomal Recessive Spastic Paraplegia Type 35 | Autosomal Recessive Bestrophinopathy | Patent Ductus Arteriosus | Spasticity | Atherosclerosis | Syndactyly | Neurofibromatosis-Noonan Syndrome | Vertigo | Angelman Syndrome | Tyrosinemia Type 1 | Metabolic Syndrome | Malnutrition | Shock, Cardiogenic | Sweet Syndrome | Norrie Disease | Prostatitis | Chediak-Higashi Syndrome | Hyperoxaluria | Batten Disease | Metatropic Dysplasia | Alpha-thalassemia Myelodysplasia Syndrome | Tonsillitis | Pseudoexfoliation Syndrome | Xeroderma Pigmentosum Variant Type | Basan Syndrome | Primary Progressive Nonfluent Aphasia | Osteoglophonic Dysplasia | Waardenburg Syndrome Type 1 | Dyslipidemia | Acanthosis Nigricans | Seborrheic Dermatitis | D-2-Hydroxyglutaric Aciduria | Pyruvate Carboxylase Deficiency Disease | Nail Disorder, Nonsyndromic Congenital | Thromboembolism | Primary Lateral Sclerosis | Familial Mediterranean Fever | Autosomal Recessive Congenital Ichthyosis | Cholangitis | Gastroschisis | Chloridorrhea, Congenital | Neuroma | Jacobsen Syndrome | Choriocarcinoma | N-acetylglutamate Synthase Deficiency | Waardenburg Syndrome Type 2E | Cranioectodermal Dysplasia | Fontaine Progeroid Syndrome | Hereditary Hemorrhagic Telangiectasia | Multiple Sulfatase Deficiency | Poretti-Boltshauser Syndrome | Obsessive-compulsive Disorder | Moyamoya Disease | Cockayne Syndrome | Adenoma, Pituitary | Mood Disorder | Exostoses | Barakat Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Weill-Marchesani Syndrome | Spinal Muscular Atrophy Type 2 | Papillon-Lefevre Syndrome | Myelitis, Transverse | Viral Meningitis | Menkes Disease | Hemangioblastoma | Glycogen Storage Disease Type 0, Muscle | Mastitis | Arthritis | Epiphyseal Chondrodysplasia, Miura Type | Retinitis | Hypotrichosis | Achondrogenesis | Nicotine Addiction | Tinea | Pneumonia, Bacterial | Overactive Bladder | Schnyder Crystalline Corneal Dystrophy | Diabetic Encephalopathy | Hypercholesterolemia | Pituitary Disorders | VACTERL Association | Vertebrobasilar Insufficiency | Glutaric Aciduria Type 2 | Amyloidosis | Brenner Tumor | Blastomycosis | Papillorenal Syndrome | Hepatitis B, Chronic | Klinefelter Syndrome | Thrombotic Microangiopathy | Glucagonoma | Osteogenesis Imperfecta | Glycogen Storage Disease Type 1b | Lymphangioma | Clouston Hidrotic Ectodermal Dysplasia | Corticobasal Syndrome | Parkinsonism | Orthostatic Intolerance | Osteoarthritis | Dermatomyositis | Sturge-Weber Syndrome | Tumoral Calcinosis | Congenital Bile Acid Synthesis Defect | Opisthorchiasis | Eiken Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Hemosiderosis | Rhabdomyosarcoma, Alveolar | Hernia, Inguinal | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Steel Syndrome | Hypertensive Retinopathy | Hemochromatosis | Myelofibrosis | Ichthyosis Bullosa Of Siemens | Sleep Apnea | Blepharospasm | Rett Syndrome | Protein S Deficiency | Marshall-Smith Syndrome | Corneal Neovascularization | Holt-Oram Syndrome | Seizures | Chronic Leukemia | Smith-Kingsmore Syndrome | Bardet-Biedl Syndrome | Lissencephaly 2 | Ophthalmia, Sympathetic | Panniculitis | Pneumonia, Mycoplasma | Noonan Syndrome-like Disorder With Loose Anagen Hair | Ependymoma | Alazami Syndrome | Recurrent Respiratory Papillomatosis | Pathological Gambling | Paraganglioma, Carotid Body | Spinocerebellar Ataxia Type 12 | Left Ventricular Noncompaction | CHOPS Syndrome | Tardive Dyskinesia | Actinomycetoma | Leukodystrophies | Autonomic Neuropathy | Hypertension, Renal | Cannabis Abuse | Muscular Dystrophy | Cancer, Kidney | Acute Chest Syndrome | Creutzfeldt-Jakob Disease | Intracerebral Hemorrhage | Fanconi Syndrome | Schizoaffective Disorder | Filariasis | Peeling Skin Syndrome Type B | Carcinoma, Signet Ring Cell | Lentigo | Fowler's Syndrome | Chronic Lymphocytic Leukemia | Primary Ovarian Insufficiency | Von Hippel-Lindau Disease | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Lassa Fever | Acrodermatitis Enteropathica | Meleda Disease | Hypermetropia | Mitochondrial Cytopathy | Alopecia | Pulmonary Stenosis | ICF Syndrome | Erythematotelangiectatic Rosacea | Epidermolytic Hyperkeratosis | Arthritis, Reactive | Juvenile Hyaline Fibromatosis | Duchenne Muscular Dystrophy | Muir-Torre Syndrome | Cancer, Lung | Analgesia | Charcot-Marie-Tooth Disease, Type 6 | Encephalitis | Tibial Muscular Dystrophy | Arrhythmogenic Right Ventricular Cardiomyopathy | Pregnancy, Ectopic | Nasodigitoacoustic Syndrome | Hypercalcemia | Generalized Epilepsy With Febrile Seizures Plus | DEND Syndrome | Proctitis | Anterior Segment Dysgenesis | Spinocerebellar Ataxia Type 3 | Loeys-Dietz Syndrome Type 4 | Charcot-Marie-Tooth Disease, Type 2C | Gingivitis | Bipolar Disorder | Apert Syndrome | Rubeosis Iridis | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Non-epidermolytic Palmoplantar Keratoderma | Charcot-Marie-Tooth Disease Type 2T | Prolidase Deficiency | Stickler Syndrome | Congenital Nystagmus | Diffuse Mesangial Sclerosis | Tendinitis | Nephropathy | Cervical Dystonia | Epidermolysis Bullosa Simplex, Generalized | Plasmacytoma | Behavioral Variant Of Frontotemporal Dementia | Angiosarcoma Of The Breast | Megaloblastic Anemia | Progressive External Ophthalmoplegia | Fabry's Disease | Traboulsi Syndrome | Tinea Versicolor | Pre-eclampsia | Micropenis | Proteus Syndrome | Carcinoma, Transitional Cell | Aplastic Anemia | Ganglioglioma | Bruck Syndrome | Nicolaides-Baraitser Syndrome | Low Tension Glaucoma | Lymphoma, AIDS-related | Sick Sinus Syndrome 1 | Hypercholesterolemia, Familial | Chromosome 17q21.31 Deletion Syndrome | Graves Disease | Mitochondrial DNA Depletion Syndrome | Preaxial Polydactyly | Wolfram Syndrome | Cholesteryl Ester Storage Disease | Sarcoma, Endometrial Stromal | Split Hand-foot Malformation | Atopic Dermatitis | Delirium | Generalized Epilepsy And Paroxysmal Dyskinesia | Whipple's Disease | Coronary Heart Disease | Angiodysplasia | T-cell Prolymphocytic Leukemia | Ameloblastic Carcinoma | Neutrophilia | Beckwith-Wiedemann Syndrome | Prolactinoma | Methylmalonic Acidemia | Myositis, Focal | Takayasu's Arteritis | Eosinophilic Asthma | Renpenning Syndrome | Cervicitis | Rothmund-Thomson Syndrome | Astrocytoma, Anaplastic | Trichothiodystrophy | Scleroderma, Diffuse | Dengue Hemorrhagic Fever | Retinitis Pigmentosa | Diabetes Mellitus, Transient Neonatal | Usher Syndrome Type II | Hidradenitis | Spinocerebellar Ataxia Type 1 | Osteopetrosis | Pemphigus Vulgaris | Androgen Insensitivity | Optic Atrophy 2 | Gastroenteritis | Menetrier Disease | Seasonal Mood Disorder | Skin Papilloma | Schwartz-Jampel-Aberfeld Syndrome | Meier-Gorlin Syndrome | Chiari Malformation Type I | Heterotopic Ossification | Bloom Syndrome | Fragile X Syndrome | Pelvic Inflammatory Disease | Pleomorphic Xanthoastrocytoma | Lymphoma Lymphoblastic | Progressive Familial Intrahepatic Cholestasis Type 1 | Frank-ter Haar Syndrome | Hypogonadism | Uterine Leiomyoma | Hypospadias | Spinocerebellar Ataxia Type 14 | Heart Block | Spinocerebellar Ataxia Type 21 | Echinococcosis | Amelogenesis Imperfecta | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Retinal Degeneration | Paroxysmal Nocturnal Hemoglobinuria | Dermatitis | Vulvovaginitis | Basal Cell Nevus Syndrome | Congenital Dysfibrinogenemia | Hypertelorism | Coloboma | Rash | Chylothorax, Congenital | Otosclerosis | Hyperlipidemia, Familial Combined | Scleroderma | Meningeal Melanocytoma | Scabies | Renal Medullary Carcinoma | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Torticollis | Aldosterone Synthase Deficiency | Obesity | Cerebral Cavernous Malformations | Demyelinating Diseases | Perivascular Epithelioid Cell Tumor | Osteomalacia | Histiocytosis | Lipodystrophy