Stuve-Wiedemann Syndrome

About the Disease
Stuve-Wiedemann Syndrome 1, also known as stuve-wiedemann syndrome, is related to leukemia and sturge-weber syndrome, and has symptoms including apnea and hoarseness. An important gene associated with Stuve-Wiedemann Syndrome 1 is LIFR (LIF Receptor Subunit Alpha), and among its related pathways/superpathways are NFAT and Cardiac Hypertrophy and Translation Insulin regulation of translation. Affiliated tissues include bone, tongue and eye, and related phenotypes are hyperhidrosis and skeletal dysplasia

Common Targets
TENT5A | LIFR

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

Other Diseases

Cleidocranial Dysplasia | Congenital Heart Block | Sturge-Weber Syndrome | Metabolic Syndrome | Rhizomelic Chondrodysplasia Punctata | Periventricular Leukomalacia | Glomerulonephritis | Weill-Marchesani Syndrome | Learning Disability | Periodic Limb Movement Disorder | Gitelman Syndrome | Castleman Disease | Basal Ganglia Disease, Biotin-responsive | Hereditary Elliptocytosis | Congestive Heart Failure | Hyperthyroidism | Epidermodysplasia Verruciformis | Temtamy Preaxial Brachydactyly Syndrome | Dementia, Vascular | Glucagonoma | Anosmia, Congenital | Osteogenesis Imperfecta Type II | Erythema Multiforme | Rheumatoid Arthritis | Esotropia | Usher Syndrome | Leiomyosarcoma | DICER1 Syndrome | Asthma | Barakat Syndrome | Peutz-Jeghers Syndrome | Dystonia | Mucolipidosis Type IV | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Autoimmune Disease | Ellis-Van Creveld Syndrome | Marfan Syndrome | Harlequin Ichthyosis | Ureteropelvic Junction Obstruction | Dyggve-Melchior-Clausen Disease | Hypercholesterolemia | Carbamoyl Phosphate Synthetase I Deficiency | Dysthymia | Hypercalcemia | Coffin-Siris Syndrome | Lymphangiomatosis | Retinitis | Fatty Aldehyde Dehydrogenase Deficiency | Angina Pectoris | Ameloblastoma | Trichomegaly | Homocystinuria | Angioedema | MELAS Syndrome | Dentinogenesis Imperfecta | Corneal Dystrophies, Hereditary | Bulimia Nervosa | Pyruvate Dehydrogenase Deficiency | Nestor-Guillermo Progeria Syndrome | Cold Agglutinin Disease | Rift Valley Fever | Infectious Diarrhea | Asperger Syndrome | Cranial Nerve Disease | Dyslipidemia | Waardenburg Syndrome Type 2E | Mucolipidosis | Leprosy | Lissencephaly 2 | Charcot-Marie-Tooth Disease Type 4 | Angiodysplasia | Muckle-Wells Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Stiff-man Syndrome | Vascular Calcification | Coenzyme Q10 Deficiency | Thanatophoric Dysplasia | Niemann-Pick Disease | Fukuyama Congenital Muscular Dystrophy | Bullous Pemphigoid | Vitamin A Deficiency | Urolithiasis | Dengue Hemorrhagic Fever | Megalencephaly | Vitreoretinopathy, Proliferative | Sponastrime Dysplasia | Chordoid Glioma | Pearson Syndrome | Sjogren Syndrome | Blue Nevus | Hennekam Lymphangiectasia-lymphedema Syndrome | Mastitis | Pneumonia, Mycoplasma | Woodhouse-Sakati Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Epilepsy | Rhabdoid Tumor | Kearns-Sayre Syndrome | Sarcoidosis | Tyrosinemia | Hyperostosis | Colitis | Arts Syndrome | Hyperprolactinemia | Encephalopathy, Hepatic | Hepatitis C, Chronic | Anxiety Disorders | Pseudomyxoma Peritonei | Tinea | Cranioectodermal Dysplasia | Osteogenesis Imperfecta Type III | Polymyalgia Rheumatica | Neuroblastoma | Ectrodactyly | Pemphigus | Histoplasmosis | Familial Advanced Sleep Phase Syndrome | Spinocerebellar Ataxia Type 8 | Wieacker-Wolff Syndrome | Thrombasthenia | Amenorrhea | Tetraplegia | Mannosidase Deficiency Diseases | Diabetes Type 1 | Loeys-Dietz Syndrome | Arthritis, Reactive | Cryptococcal Meningitis | Aspartylglycosaminuria | Pseudo-pseudohypoparathyroidism | Pericarditis | Nail Disorder, Nonsyndromic Congenital | Hypobetalipoproteinemias | Acromicric Dysplasia | Dysferlinopathy | Bardet-Biedl Syndrome | Exfoliative Dermatitis | Astigmatism | Superficial Spreading Melanoma | Combined Pituitary Hormone Deficiency | Osteoarthritis | Primary Torsion Dystonia | Epidermolysis Bullosa Acquisita | Pyruvate Kinase Deficiency | Aarskog-Scott Syndrome | Peyronie's Disease | Progressive Familial Intrahepatic Cholestasis Type 2 | LRBA Deficiency | Specific Granule Deficiency | Congenital Heart Defects | Oligoasthenoteratozoospermia | Dupuytren Disease | Sweet Syndrome | Early Infantile Epileptic Encephalopathy 1 | Keloid | Vitreoretinal Degeneration, Snowflake Type | Ganglioglioma | Knobloch Syndrome | Spasticity | Interstitial Lung Diseases | Toxoplasmosis | Cone Dystrophy | Carpenter Syndrome | Seizures | Liver Diseases | Cardiac Arrest | Cancer, Kidney | Borderline Personality Disorder | Episodic Ataxia Type 1 | Hypertelorism | Photosensitivity | Corticobasal Syndrome | Impulse Control Disorder | Angelman Syndrome | Aromatic L-amino Acid Decarboxylase Deficiency | Moyamoya Disease | Sotos Syndrome | CDKL5 Deficiency Disorder | Melanoma, Malignant | Meesmann Corneal Dystrophy | Osteosarcoma | Cardiac Sarcoidosis | Dementia | Blau Syndrome | Cancer, Lung | Avellino Corneal Dystrophy | Paraganglioma, Carotid Body | Esophagitis, Eosinophilic | Juvenile Myoclonic Epilepsy | Congenital Disorders Of Glycosylation | Hyper IgE Syndrome | Gestational Trophoblastic Disease | Arteriovenous Malformations | Gout | Retinoblastoma | Persistent Hyperplastic Primary Vitreous | Atherosclerosis | Vertebrobasilar Insufficiency | Meningitis | Bartter Syndrome | Branchiootorenal Syndrome | Pierson Syndrome | Sickle Cell Anemia | Trichothiodystrophy | Skin Fragility-woolly Hair Syndrome | Porphyria | Nicolaides-Baraitser Syndrome | Polycythemia Vera | SAPHO Syndrome | Canavan Disease | Impetigo | Chromosome 9q34.3 Deletion Syndrome | Stroke, Hemorrhagic | Phenylketonuria II | Multiple Sclerosis, Chronic Progressive | Wagner Disease | Autoimmune Polyendocrinopathy Syndrome Type I | Creatine Deficiency Syndrome Due To AGAT Deficiency | Hereditary Hemorrhagic Telangiectasia | Leukocyte Adhesion Deficiency Type 1 | Trigonocephaly | Encephalitis | X-linked Charcot-Marie-Tooth Disease | Dominant Optic Atrophy | Adenylosuccinate Lyase Deficiency | Trachoma | Netherton Syndrome | Frank-ter Haar Syndrome | Chronic Mucocutaneous Candidiasis | Actinomycetoma | Primary Lateral Sclerosis | Cataract | Pseudohypoparathyroidism Type 2 | Fabry's Disease | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Congenital Bile Acid Synthesis Defect | Tyrosine Hydroxylase Deficiency | Corneal Dystrophy | Posterior Polar Cataract | Mandibuloacral Dysplasia With Type A Lipodystrophy | Optic Atrophy 2 | Meconium Ileus | Hepatoblastoma | GLUT1 Deficiency Syndrome | Cutaneous Angiosarcoma | Acromegaly | Prader-Willi Syndrome | Cardiofaciocutaneous Syndrome | Conduct Disorder | Familial Cerebral Amyloid Angiopathy | Poirier-Bienvenu Neurodevelopmental Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Stickler Syndrome | Renal Hypomagnesemia 3 | Hemolytic Anemia | Lymphangioma | Tangier Disease | Aldosterone Deficiency | Spinocerebellar Ataxia Type 3 | Central Core Disease | Schistosomiasis | Juvenile Myelomonocytic Leukemia | Cenani-Lenz Syndactyly Syndrome | Leri Pleonosteosis | Presbycusis | Usher Syndrome Type I | Nephrosclerosis | Hydrocephalus, Normal Pressure | Extramammary Paget's Disease | Primary Sclerosing Cholangitis | Transient Bullous Dermolysis Of The Newborn | Open-angle Glaucoma | Microphthalmia, Syndromic 7 | Pleomorphic Xanthoastrocytoma | Low Tension Glaucoma | Presbyopia | Fundus Albipunctatus | Benign Familial Pemphigus | Distal Spinal Muscular Atrophy | X-linked Myotubular Myopathy | Hyperkeratosis | Idiopathic Multicentric Castleman Disease | Evans Syndrome | Osteopetrosis | Pontocerebellar Hypoplasia Type 2 | Thalassemia | Hemophagocytic Lymphohistiocytosis | Multiple Sclerosis, Secondary Progressive | Chronic Lymphocytic Leukemia | Autosomal Recessive Spastic Paraplegia Type 54 | Double Outlet Right Ventricle | Myelofibrosis | Glutaric Aciduria Type 3 | Nutrition Disorders | VACTERL Association | Psoriasis | Hypocalcemia | Blepharophimosis Syndrome | Myositis, Focal | Malignant Fibrous Histiocytoma | Congenital Poikiloderma | Autoimmune Autonomic Ganglionopathy | Myocarditis | Birk-Barel Syndrome | Charcot-Marie-Tooth Disease Type 4B1 | Hyperinsulinemia | Focal Cortical Dysplasia Type 2 | Blepharitis | Agammaglobulinemia | Paget's Disease Of The Breast | Sengers Syndrome | Reye Syndrome | Hodgkin Lymphoma | Porokeratosis | Glutaric Aciduria Type 1 | Placenta Previa | Pierpont Syndrome | Congenital Myasthenic Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Charcot-Marie-Tooth Disease Type 2E | Metanephric Adenoma | Epidermolytic Ichthyosis, Annular | Episodic Ataxia | Lysosomal Acid Lipase Deficiency | Chronic Inflammatory Demyelinating Polyneuropathy | Spondyloperipheral Dysplasia | Fanconi Syndrome | Cholelithiasis | C3 Glomerulopathy | Ebstein Anomaly | Fetal And Neonatal Alloimmune Thrombocytopenia | Malaria, Cerebral | Kohlschutter-Tonz Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Sclerosteosis 2 | Congenital Afibrinogenemia | Bone Giant Cell Tumor | Stevens-Johnson Syndrome | Absence Epilepsy | Lymphoproliferative Disease, X-linked | Juvenile Xanthogranuloma | Charcot-Marie-Tooth Disease Axonal Type 2N | Adrenal Insufficiency | Kabuki Syndrome | Meier-Gorlin Syndrome | Alpha-mannosidosis | Early Infantile Epileptic Encephalopathy 4 | KBG Syndrome | Giant Cell Glioblastoma | Omenn Syndrome | Myofibromatosis | Neuroma | Jacobsen Syndrome | Bronchitis, Chronic | Skin Papilloma | Menetrier Disease | Hyperkalemic Periodic Paralysis | Alcoholism | Ghosal Syndrome | Gastritis | Greenberg Dysplasia | Alexander Disease | Rhabdomyosarcoma, Embryonal | Spinocerebellar Ataxia Type 28 | Ichthyosis, X-linked | Hereditary Mixed Polyposis Syndrome | Coloboma | Osteogenesis Imperfecta Type VI | GM2-gangliosidosis AB Variant | Emery-Dreifuss Muscular Dystrophy | Cancer, Colon | Myhre Syndrome | Optic Nerve Hypoplasia, Bilateral | Diffuse Intrinsic Pontine Glioma | Mixed Connective Tissue Disease | Osteogenesis Imperfecta Type I | Leri-Weill Dyschondrosteosis | Optic Neuropathy | B-cell Prolymphocytic Leukemia | Congenital Disorders Of Glycosylation Type II | Acrodysostosis | Gastroenteritis, Eosinophilic | Progressive Myoclonic Epilepsy | Acute Myeloid Leukemia | Carotid Artery Disease | Postaxial Polydactyly | Rheumatic Heart Disease | Rett Syndrome | Hypervalinemia | Bethlem Myopathy | Hypotrichosis | Acute Lung Injury | Uveitis, Anterior | Celiac Disease | Mucormycosis | Dysequilibrium Syndrome | Orthostatic Intolerance | Tonsillitis | Tenosynovial Giant Cell Tumor | Primary Hyperoxaluria | Sensorineural Hearing Loss