Sponastrime Dysplasia
Sponastrime Dysplasia
About the Disease
Spondyloepimetaphyseal Dysplasia, Sponastrime Type, also known as sponastrime dysplasia, is related to spondyloepimetaphyseal dysplasia and metaphyseal dysplasia. An important gene associated with Spondyloepimetaphyseal Dysplasia, Sponastrime Type is TONSL (Tonsoku Like, DNA Repair Protein). Affiliated tissues include bone, and related phenotypes are depressed nasal bridge and platyspondyly
Common Targets
TONSL

Note: If you'd like to get a target analysis report for Sponastrime Dysplasia, 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 Sponastrime Dysplasia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Congenital Myopathy | H Syndrome | Frank-ter Haar Syndrome | Rothmund-Thomson Syndrome | Glycogen Storage Disease Type 1 | D-2-Hydroxyglutaric Aciduria | Mesothelioma, Malignant | Pterygium | Noonan Syndrome-like Disorder With Loose Anagen Hair | Autosomal Recessive Spastic Paraplegia Type 54 | Lymphopenia | Charcot-Marie-Tooth Disease Type 4D | Hydrocephalus, Normal Pressure | Periodontitis | Spinocerebellar Ataxia Type 21 | Combined Deficiency Of Factor V And Factor VIII | Exfoliative Dermatitis | Carcinoma, Signet Ring Cell | Chronic Idiopathic Myelofibrosis | Cysticercosis | Persistent Fetal Circulation | Migraine | Spondylo-ocular Syndrome | Corneal Dystrophies, Hereditary | Myotonic Disorders | Birt-Hogg-Dube Syndrome | Presbycusis | Myofibromatosis | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Cannabis Abuse | Hypertension, Renal | Aldosterone Deficiency | Thalassemia | Hepatitis | Mevalonate Kinase Deficiency | Prostatitis | Twin-to-twin Transfusion Syndrome | Microcephaly, Seizures, And Developmental Delay | Pleomorphic Xanthoastrocytoma | Hyperkalemic Periodic Paralysis | Hepatic Adenomatosis | Teratozoospermia | Cardiac Sarcoidosis | Pyruvate Dehydrogenase Deficiency | Eczema | X-linked Charcot-Marie-Tooth Disease | Myelodysplasia | Otopalatodigital Syndrome Type 2 | Leishmaniasis, Cutaneous | Hyperacusis | Ligneous Conjunctivitis | Beckwith-Wiedemann Syndrome | Li-Fraumeni Syndrome | Tic Disorder | Focal Dermal Hypoplasia | Papilloma | Meningococcal Infections | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Spinocerebellar Ataxia Type 5 | Syphilis | DOCK8 Immunodeficiency Syndrome | Hypopigmentation | Holt-Oram Syndrome | Scleroderma | GLUT1 Deficiency Syndrome | Paraplegia | Obsessive-compulsive Disorder | Osteitis | Occipital Neuralgia | Jawad Syndrome | Thalassemia, Beta | Hyperglycemia | Tardive Dyskinesia | Blepharoconjunctivitis | Cyclic Vomiting Syndrome | Graves Disease | Hairy Cell Leukemia | Walker-Warburg Syndrome | Arthropathy | Pigment Dispersion Syndrome | Spinocerebellar Ataxia Type 15 | Wilson's Disease | Binge Eating Disorder | Pituitary Disorders | Leishmaniasis, Visceral | Urofacial Syndrome | Leiomyosarcoma | Saul-Wilson Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Familial Glucocorticoid Deficiency | Coenzyme Q10 Deficiency | SAPHO Syndrome | Lymphoproliferative Disease, X-linked | Autonomic Neuropathy | Lymphoma, Mantle Cell | Recurrent Respiratory Papillomatosis | Carcinoid Syndrome | Limb Girdle Muscular Dystrophy | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Goiter, Nodular | Subcortical Band Heterotopia | Congenital Stromal Corneal Dystrophy | Fuchs Heterochromic Iridocyclitis | Congenital Disorders Of Glycosylation | Multicystic Renal Dysplasia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Juvenile Xanthogranuloma | Gyrate Atrophy Of The Choroid And Retina | POEMS Syndrome | Hemolytic Uremic Syndrome, Atypical | Motor Neuron Diseases | Thrombocytopenia | Ophthalmia, Sympathetic | Agranulocytosis | Hypoparathyroidism | Hypotonia-cystinuria Syndrome | Familial Hyperaldosteronism | Periventricular Leukomalacia | Renal Tubular Acidosis | Lymphoma, AIDS-related | Crisponi Syndrome | Diastrophic Dysplasia | Primary Progressive Aphasia | Fibromuscular Dysplasia | Superficial Spreading Melanoma | Seborrheic Dermatitis | Optic Neuropathy, Anterior Ischemic | Hyperlipidemia Type V | Primary Carnitine Deficiency | Hereditary Spastic Paraplegia | Meningococcal Meningitis | Chromosome 9q34.3 Deletion Syndrome | Leber Hereditary Optic Neuropathy | Sotos Syndrome | Dysequilibrium Syndrome | Dyggve-Melchior-Clausen Disease | Peritonitis | Sjogren Syndrome | Leukemia-lymphoma, Adult T-cell | Polycythemia | Hartsfield Syndrome | Lactose Intolerance | Cheilitis | Myeloid Leukemia | Goldenhar Syndrome | Polycystic Kidney, Autosomal Recessive | Pulmonary Veno-occlusive Disease | Erythromelalgia | Barakat Syndrome | C3 Glomerulonephritis | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Adrenal Insufficiency | Inflammatory Joint Disease | Encephalitis, Tick-borne | Sitosterolemia | Presbyopia | Acrocallosal Syndrome | Language Disorders | Alpha-mannosidosis | Menkes Disease | AIDS | Saethre-Chotzen Syndrome | Encephalopathy | Hypotrichosis Simplex | Carcinoma, Transitional Cell | Multiple Sclerosis, Primary Progressive | Chronic Beryllium Disease | Tylosis With Esophageal Cancer | Kohlschutter-Tonz Syndrome | Acne Vulgaris | Takayasu's Arteritis | Gestational Trophoblastic Disease | Ureteropelvic Junction Obstruction | Pierpont Syndrome | Argininosuccinic Aciduria | Glycogen Storage Disease Type 3 | Microphthalmia | Acral Lentiginous Melanoma | Communication Disorders | Cranial Nerve Disease | Keratosis, Actinic | Cold-induced Sweating Syndrome | Jaundice, Obstructive | Myhre Syndrome | Myopathy | Heterotopic Ossification | Spinocerebellar Ataxia Type 27 | Perivascular Epithelioid Cell Tumor | Cholestasis, Intrahepatic | Diabetic Encephalopathy | Dysmorphophobia | Ocular Surface Squamous Neoplasia | Hermansky-Pudlak Syndrome | Androgen Insensitivity | Myositis | Mucolipidosis | Mitochondrial Encephalomyopathy | Chronic Thromboembolic Pulmonary Hypertension | Sezary Syndrome | Nemaline Myopathy 8 | Empyema | Pupil Disorders | Hemophilia | Senior-Loken Syndrome | Hidradenitis | Long QT Syndrome Type 1 | Amelanotic Melanoma | Corneal Ulcer | Greig Cephalopolysyndactyly Syndrome | Nevus | Rift Valley Fever | Idiopathic Pulmonary Fibrosis | Arthritis, Gouty | Creutzfeldt-Jakob Disease | Antisocial Personality Disorder | Acromegaly | Pelizaeus-Merzbacher Disease | Alpers Syndrome | Glutaric Aciduria Type 1 | Spina Bifida | Seasonal Mood Disorder | Usher Syndrome | Keratosis, Seborrheic | Pathological Gambling | Liver Failure | Melanoma, Uveal | Angioedema, Hereditary | Neuroleptic Malignant Syndrome | Bietti Crystalline Dystrophy | Prurigo Nodularis | Osteomalacia | Celiac Disease | Hyperkeratosis | Trigonocephaly | Ichthyosis | Acute Lung Injury | Bernard-Soulier Syndrome | Chronic Neutrophilic Leukemia | Danon Disease | Choroideremia | DICER1 Syndrome | Congenital Hypofibrinogenemia | Diabetes Insipidus, Neurogenic | Transient Bullous Dermolysis Of The Newborn | Nicolaides-Baraitser Syndrome | Pontocerebellar Hypoplasia | Menetrier Disease | Rhabdomyosarcoma, Alveolar | Spinocerebellar Ataxia Type 20 | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Sarcoidosis, Pulmonary | Congenital Diaphragmatic Hernia | Trismus-pseudocamptodactyly Syndrome | Schizophrenia | Tatton-Brown-Rahman Syndrome | Rolandic Epilepsy | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Peutz-Jeghers Syndrome | Potocki-Shaffer Syndrome | Chronic Myeloid Leukemia | Shprintzen-Goldberg Syndrome | Pantothenate Kinase-associated Neurodegeneration | Prune Belly Syndrome | Myelofibrosis | Hyperammonemia | Adenomyosis | Tracheal Disorders | Geleophysic Dysplasia | Pyloric Stenosis, Infantile Hypertrophic | Multisystemic Smooth Muscle Dysfunction Syndrome | Adenylosuccinate Lyase Deficiency | Congenital Adrenal Hyperplasia 1 | Hyperandrogenemia | Cholestasis | Alopecia Areata | Hemolytic Anemia | Polydactyly | Pulmonary Sclerosing Hemangioma | Primary Hyperoxaluria Type 3 | Hypolipoproteinemia | Sleep Apnea, Central | Stiff-man Syndrome | Angiosarcoma Of The Breast | Oligoastrocytoma | Bronchiectasis | Maternally Inherited Diabetes And Deafness | Fibrosarcoma | Abetalipoproteinemia | CHOPS Syndrome | Acromicric Dysplasia | Diverticulitis | Primary Pigmented Nodular Adrenocortical Disease | Hyperlipidemia, Familial Combined | Gliosarcoma | Retinal Dystrophy | Diffuse Mesangial Sclerosis | Sensorineural Hearing Loss | Pemphigus | Congenital Central Hypoventilation Syndrome | Waardenburg Syndrome Type 2 | Waardenburg Syndrome Type 1 | Xeroderma Pigmentosum Variant Type | Renal Failure | Osteopathia Striata With Cranial Sclerosis | Pleural Tuberculosis | Sengers Syndrome | Autoimmune Disease | Pendred Syndrome | Primary Torsion Dystonia | Schamberg Disease | Still Disease | Tendinitis | Congestive Heart Failure | Thin Basement Membrane Disease | Hyperparathyroidism-jaw Tumor Syndrome | Cantu Syndrome | Bladder Exstrophy | Porokeratosis | Anuria | Cryopyrin-associated Periodic Syndromes | Lymphangioleiomyomatosis | Hemangioendothelioma | Astrocytoma | Anthrax | Leukocyte Adhesion Deficiency | Dupuytren Disease | Sarcoma, Alveolar Soft Part | Epidermolytic Ichthyosis, Annular | Alcoholism | Trichorhinophalangeal Syndrome | Opisthorchiasis | Essential Fructosuria | Tremor | Malnutrition | Avian Influenza | Primary Cutaneous Amyloidosis | B-cell Chronic Lymphocytic Leukemia | Lymphangiomatosis | Congenital Dyserythropoietic Anemia | Actinomycetoma | Mastitis | Hypertrophy | Pituitary Dwarfism | Infectious Diarrhea | Pyruvate Carboxylase Deficiency Disease | Granuloma Annulare | Light Chain Amyloidosis | Dystrophy, Cone-rod | Histiocytic Sarcoma | Hypoplastic Left Heart Syndrome | Analgesia | Guillain-Barre Syndrome | Panic Disorder | Oculocutaneous Albinism Type 1 | Osteogenesis Imperfecta Type I | Cutaneous Angiosarcoma | Polyneuropathy | Lymphomatoid Granulomatosis | Rubinstein-Taybi Syndrome | Pyoderma Gangrenosum | Emery-Dreifuss Muscular Dystrophy | Sclerosteosis 2 | Parvovirus B19 Infection | Glucagonoma | Spinal Cord Diseases | Osteogenesis Imperfecta Type IV | Beta-Propeller Protein-associated Neurodegeneration | Eosinophilic Asthma | Avellino Corneal Dystrophy | Hyperlipidemia | Thrombosis | Constipation | Narcolepsy | Anxiety Disorders | Brooke-Spiegler Syndrome | Hyperphenylalaninemia | Parapsoriasis | Malignant Peripheral Nerve Sheath Tumor | Motion Sickness | Open-angle Glaucoma | Porencephaly | Hypothalamic Obesity | Aceruloplasminemia | Cryptococcal Meningitis | Chondrodysplasia Punctata 1, X-linked Recessive | Amish Infantile Epilepsy Syndrome | Hypohidrotic Ectodermal Dysplasia, X-linked | Nephritis, Interstitial | Cellulitis | Polycystic Kidney, Autosomal Dominant | Nutrition Disorders | Tendinopathy | Cartilage Disorders | Schnyder Crystalline Corneal Dystrophy | Glycogen Storage Disease Type 5 | Anosmia, Congenital | Neuroendocrine Cancer | Aldosterone Synthase Deficiency | Scleritis