Reticular Dysgenesis

About the Disease
Immunoerythromyeloid Hypoplasia, is also known as reticular dysgenesis. The drugs Cyclophosphamide and Fludarabine have been mentioned in the context of this disorder. Affiliated tissues include myeloid, and related phenotypes are decreased circulating igg level and lymphoproliferative disorder

Common Targets
AK2 | USF1 | TCIRG1

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Other Diseases

Reticular Dysgenesis | DRESS Syndrome | Knobloch Syndrome | C3 Glomerulopathy | Epidermal Nevus Syndrome | Peutz-Jeghers Syndrome | Hypervalinemia | Marshall-Smith Syndrome | Hemophilia | Coffin-Lowry Syndrome | Focal Cortical Dysplasia Type 2 | Asphyxia Neonatorum | Blau Syndrome | Lentigo | Takayasu's Arteritis | Tuberculous Meningitis | Congenital Fiber-type Disproportion Myopathy | Craniofrontonasal Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | D-2-Hydroxyglutaric Aciduria | Autoimmune Hemolytic Anemia | Pyruvate Carboxylase Deficiency Disease | Pneumonia, Bacterial | Hypogonadism | Peeling Skin Syndrome, Acral Type | Hypogammaglobulinemia | Bietti Crystalline Dystrophy | Carotid Artery Disease | CREST Syndrome | Erythrokeratodermia Variabilis | Localized Scleroderma | Paraganglioma | Glaucomatocyclitic Crisis | Diabetes | Hypokalemia | Craniosynostosis | Dermatitis | Glucagonoma | Follicular Dendritic Cell Sarcoma | Myoclonic Epilepsy With Ragged Red Fibers | Renal-hepatic-pancreatic Dysplasia | Peritonitis | Bardet-Biedl Syndrome | Acute Anterior Uveitis | POEMS Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Spinocerebellar Ataxia Type 10 | Acute Myeloid Leukemia | Vasculitis | C3 Glomerulonephritis | Microtia | Apraxia | B-cell Prolymphocytic Leukemia | Malaria | Becker Muscular Dystrophy | Cerebellar Ataxia, Cayman Type | Spinocerebellar Ataxia Type 23 | Werner's Syndrome | Retinal Vasculitis | Milk Allergy | Glycogen Storage Disease Type 4 | Porphyria, Acute Intermittent | Renal Oncocytoma | Swine Influenza | Primary Hyperoxaluria Type 3 | Central Retinal Artery Occlusion | Paraplegia | Portal Vein Thrombosis | Norrie Disease | Amyotrophic Lateral Sclerosis, Juvenile | Kaposi Sarcoma | Postpoliomyelitis Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Common Cold | Hypertelorism | Ebstein Anomaly | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Schnyder Crystalline Corneal Dystrophy | Chronic Enteropathy Associated With SLCO2A1 Gene | Myofibromatosis | Headache | Granular Corneal Dystrophy Type 1 | Hereditary Elliptocytosis | Cranioectodermal Dysplasia | Cantu Syndrome | Meningococcal Meningitis | Tatton-Brown-Rahman Syndrome | Anodontia | Anti-glomerular Basement Membrane Disease | Noonan Syndrome | Mucolipidosis Type IV | Cold Agglutinin Disease | GAPO Syndrome | Premature Ejaculation | Brugada Syndrome 1 | Endophthalmitis | Alopecia Areata | Leishmaniasis, Visceral | Gastroenteritis | Agranulocytosis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Myocardial Infarction | Adult Polyglucosan Body Disease | Mast Cell Leukemia | Focal Segmental Glomerulosclerosis | Pulmonary Alveolar Proteinosis | Hepatitis, Chronic | Glycogen Storage Disease Type 0, Muscle | Mumps | Autoimmune Polyendocrinopathy Syndrome Type I | Succinic Semialdehyde Dehydrogenase Deficiency | Sandhoff Disease | Sengers Syndrome | Metachromatic Leukodystrophy | Addison Disease | Low Tension Glaucoma | DICER1 Syndrome | Phenylketonuria II | Nephroblastoma | Glanzmann Thrombasthenia | Spondylosis | Hyperekplexia | CDKL5 Deficiency Disorder | Uveitis, Anterior | Graft-versus-host Disease | Dyggve-Melchior-Clausen Disease | Depression | Pleural Tuberculosis | Trigonocephaly | Congenital Hemolytic Anemia | Harlequin Ichthyosis | Creutzfeldt-Jakob Disease | Varicocele | Pelizaeus-Merzbacher Disease | Cerebellofaciodental Syndrome | Narcolepsy | Large Granular Lymphocytic Leukemia | Tumoral Calcinosis | Bipolar Disorder | Micro Syndrome | Plasma Cell Dyscrasia | Osteitis | Metabolic Diseases | Primary Erythromelalgia | Gestational Trophoblastic Disease | Tardive Dyskinesia | Juvenile Polyposis | Camptocormia | Congenital Sodium Diarrhea | Myelitis | Heroin Dependence | Infantile Spasm | Esophageal Adenocarcinoma | Focal Facial Dermal Dysplasia | Treacher Collins Syndrome | Cherubism | Nicolaides-Baraitser Syndrome | Multisystemic Smooth Muscle Dysfunction Syndrome | Calcium Pyrophosphate Deposition Disease | Tendinopathy | Arthrogryposis | Sialidosis Type I | Sporadic Hemiplegic Migraine | Inflammatory Linear Verrucous Epidermal Nevus | Deafness, Dystonia, And Cerebral Hypomyelination | Melnick-Needles Syndrome | Encephalopathy, Hepatic | Methylmalonic Aciduria And Homocystinuria, CblC Type | Macular Degeneration | Osteochondrosis | Diabetes Type 2 | Gnathodiaphyseal Dysplasia | Epidermolysis Bullosa Simplex, Localized | Myoclonic Atonic Epilepsy | Melanoma, Malignant | Tracheal Disorders | Leukocyte Adhesion Deficiency Type 1 | Distal Myopathy 2 | Bruck Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Desmosterolosis | Neurofibromatosis Type 2 | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Thymoma, Malignant | Corneal Edema | VEXAS Syndrome | Chromosome 17q21.31 Deletion Syndrome | CHARGE Syndrome | Neuroma | Campomelic Dysplasia | Scoliosis | Centronuclear Myopathy | Mixed Connective Tissue Disease | Lymphoma, AIDS-related | Leukoplakia | Malnutrition | Situs Inversus | Meconium Ileus | Cancer, Prostate | X-linked Charcot-Marie-Tooth Disease | Paternal Uniparental Disomy Of Chromosome 14 | Loeys-Dietz Syndrome Type 4 | Patent Foramen Ovale | Perivascular Epithelioid Cell Tumor | Lymphangioma | Cockayne Syndrome | Rheumatic Heart Disease | ACTH-independent Macronodular Adrenal Hyperplasia | Hereditary Hemorrhagic Telangiectasia Type 2 | Adrenoleukodystrophy, X-linked | Erythropoietic Protoporphyria | Sarcosinemia | Sensorineural Hearing Loss | Clouston Hidrotic Ectodermal Dysplasia | Canavan Disease | Hydronephrosis | Fatty Aldehyde Dehydrogenase Deficiency | Cardiofaciocutaneous Syndrome | Inborn Errors Of Metabolism | Malignant Peripheral Nerve Sheath Tumor | Eclampsia | Jacobsen Syndrome | Cancer, Bladder | Hyperglycemia | Cholesteryl Ester Storage Disease | Triple A Syndrome | Glioma | Pituitary Stalk Interruption Syndrome | Hyperparathyroidism, Primary | Sick Sinus Syndrome | Hereditary Sensory Neuropathy Type 1 | Juvenile Myoclonic Epilepsy | Carcinoma, Signet Ring Cell | Waardenburg Syndrome Type 1 | Withdrawal Syndrome | Diffuse Intrinsic Pontine Glioma | Retinal Telangiectasia | Alzheimer Disease, Late Onset | Short-chain Acyl-CoA Dehydrogenase Deficiency | Pain | Incontinentia Pigmenti | Kaposiform Hemangioendothelioma | Argininosuccinic Aciduria | Waardenburg Syndrome Type 2 | Genee-Wiedemann Syndrome | Chylothorax, Congenital | Schwannoma | Acute Lymphocytic Leukemia | Glycogen Storage Disease Type 1 | Behavioral Variant Of Frontotemporal Dementia | Klinefelter Syndrome | Reye Syndrome | Joubert Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Coenzyme Q10 Deficiency | Enhanced S-cone Syndrome | Trichomegaly | Pneumonia, Viral | Brooke-Spiegler Syndrome | Neural Tube Defect | Cartilage Disorders | Spinocerebellar Ataxia Type 21 | Farber Disease | Osteomalacia | Episodic Ataxia Type 1 | Myoclonus-dystonia Syndrome | Urofacial Syndrome | Paracoccidioidomycosis | Alexander Disease | Hamartoma | X-linked Creatine Transporter Deficiency | Hennekam Lymphangiectasia-lymphedema Syndrome | Aldosteronism | Primary Pigmented Nodular Adrenocortical Disease | Galactosialidosis | Congenital Hypofibrinogenemia | Liebenberg Syndrome | Osteogenesis Imperfecta Type II | Proximal Symphalangism | Schuurs-Hoeijmakers Syndrome | Dyskeratosis Congenita | Infectious Diarrhea | Pulverulent Zonular Cataract | Alveolar Capillary Dysplasia | Cystinuria | Motor Neuron Diseases | Fetal And Neonatal Alloimmune Thrombocytopenia | Pigment Dispersion Syndrome | Light Chain Amyloidosis | Kallmann Syndrome | Retinal Degeneration | Creatine Deficiency Syndrome | Inflammatory Joint Disease | Long QT Syndrome Type 2 | Spinocerebellar Ataxia | Lupus Erythematosus | Fetal Alcohol Syndrome | Cerebral Cavernous Malformations | Myelodysplasia | Cryptosporidiosis | Stargardt Disease | Goldenhar Syndrome | Schizotypal Personality Disorder | Ornithine Transcarbamylase Deficiency | Torticollis | Atopic Dermatitis | Thrombotic Microangiopathy | Blepharophimosis Syndrome | Tetanus | Stroke, Ischemic | Pityriasis Rubra Pilaris | Delirium | Leukoencephalopathy, Progressive Multifocal | Muir-Torre Syndrome | Heterotopic Ossification | Imerslund-Grasbeck Syndrome | Cleidocranial Dysplasia | Rickets | Ureteropelvic Junction Obstruction | Waldenstrom Macroglobulinemia | Adenylosuccinate Lyase Deficiency | Multicentric Carpotarsal Osteolysis Syndrome | Kohlschutter-Tonz Syndrome | Primary Biliary Cholangitis | Myocarditis | Vitamin D Deficiency | Cohen Syndrome | Renal Hypouricemia | Primary Sclerosing Cholangitis | Retinitis Pigmentosa | Hypokalemic Periodic Paralysis | Lysosomal Acid Lipase Deficiency | Hydrocephalus, Normal Pressure | Prurigo Nodularis | Fontaine Progeroid Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Branchiootorenal Syndrome | Pilomatrix Carcinoma | Bare Lymphocyte Syndrome | Tibial Muscular Dystrophy | Infantile Neuroaxonal Dystrophy | Lesch-Nyhan Syndrome | Restless Legs Syndrome | Blastomycosis | Hyperthyroidism | Atrioventricular Septal Defect | Primary Progressive Aphasia | Congenital Aniridia | Isovaleric Acidemia | Cornelia De Lange Syndrome | Congenital Afibrinogenemia | Meningococcal Infections | Analgesia | Lymphoma, Mantle Cell | Osteonecrosis | Heimler Syndrome | Polycystic Ovary Syndrome | Cervical Dystonia | Persistent Truncus Arteriosus | Spondyloepiphyseal Dysplasia Tarda, X-linked | Turner's Syndrome | Vertebrobasilar Insufficiency | Peyronie's Disease | Osteogenesis Imperfecta Type V | X-linked Myotubular Myopathy | Stuttering | Coffin-Siris Syndrome | Diabetic Macular Edema | Castleman Disease | Early Infantile Epileptic Encephalopathy | Irritable Bowel Syndrome | Shwachman-Bodian-Diamond Syndrome | Hypoalbuminemia | Papulopustular Rosacea | Okihiro Syndrome | Orthostatic Intolerance | Twin-to-twin Transfusion Syndrome | Pulmonary Stenosis | Amyloidosis | Smoldering Myeloma | Keratosis, Seborrheic | Postaxial 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