Disease

Type 3 Spondyloepimetaphyseal Dysplasia With Joint Laxity

About the Disease
Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 3, is also known as semdjl3. An important gene associated with Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 3 is EXOC6B (Exocyst Complex Component 6B). Affiliated tissues include bone, and related phenotypes are obesity and scoliosis

Common Targets
EXOC6B

疾病靶点研报
Type 3 Spondyloepimetaphyseal Dysplasia With Joint Laxity

Note: If you'd like to get a target analysis report for Type 3 Spondyloepimetaphyseal Dysplasia With Joint Laxity, 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 Type 3 Spondyloepimetaphyseal Dysplasia With Joint Laxity at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Constipation | Chondroma | Vertigo | Moyamoya Disease | Gastrointestinal Disorders | Diamond-Blackfan Anemia | Amenorrhea | Communication Disorders | Nephrotic Syndrome Type 1 | NDH Syndrome | Atelosteogenesis Type 2 | Acromegaly | Meesmann Corneal Dystrophy | Pulmonary Tuberculosis | Mevalonate Kinase Deficiency | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Familial Partial Lipodystrophy | Miyoshi Myopathy | Glycogen Storage Disease Type 0, Muscle | Hereditary Spastic Paraplegia | Chronic Neutrophilic Leukemia | Spinocerebellar Ataxia Type 13 | Carcinoma, Small Cell | Senior-Loken Syndrome | Hidradenitis | Spinal Muscular Atrophy Type 3 | Osteonecrosis | Chondrodysplasia Punctata | Craniopharyngioma | Distal Myopathy 2 | Familial Pheochromocytoma-paraganglioma | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Leukoplakia | Greenberg Dysplasia | Multiple Sclerosis, Secondary Progressive | Stickler Syndrome | Chordoma | Contact Dermatitis | Polyradiculopathy | Coronary Restenosis | Fraser Syndrome | Periventricular Leukomalacia | Glycogen Storage Disease Type 1b | Jaundice, Obstructive | Binge Eating Disorder | Anorchia | Endocarditis | Multiple Sclerosis, Chronic Progressive | Facioscapulohumeral Muscular Dystrophy Type 2 | Skin Fragility-woolly Hair Syndrome | Plasmacytoma | CHARGE Syndrome | Congenital Afibrinogenemia | Angina Pectoris | Hypohidrotic Ectodermal Dysplasia, X-linked | Congenital Myopathy | Cataract | Genitopatellar Syndrome | Amish Infantile Epilepsy Syndrome | CEDNIK Syndrome | Waardenburg Syndrome Type 4 | Hemophilia | Metaphyseal Chondrodysplasia, Schmid Type | Hepatitis D | Glycogen Storage Disease Type 5 | Choroiditis | Huntington's Disease-like 2 | Lennox-Gastaut Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Synovitis | Pyelonephritis | Retinopathy Of Prematurity | Atelosteogenesis Type 1 | Epithelioid Hemangioma | Cheilitis | Axenfeld-Rieger Syndrome | Congenital Bilateral Absence Of Vas Deferens | Myoclonic Atonic Epilepsy | Primary Sclerosing Cholangitis | Diabetes Mellitus, Transient Neonatal | Familial Dysautonomia | Glutathione Synthetase Deficiency | Molybdenum Cofactor Deficiency | Dystonia-parkinsonism, X-linked | Pseudohypoparathyroidism Type 1B | Creutzfeldt-Jakob Disease | Intermittent Explosive Disorder | Hemolytic Uremic Syndrome, Atypical | Vitamin K Deficiency | Heart Block | Paraplegia | Campomelic Dysplasia | Marinesco-Sjogren Syndrome | Aplastic Anemia | Polyneuropathy | T-cell Prolymphocytic Leukemia | C3 Glomerulopathy | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Takotsubo Cardiomyopathy | Pseudoexfoliation Syndrome | Tularemia | Cardiofaciocutaneous Syndrome | Pulmonary Alveolar Proteinosis | Erythema Multiforme | Scapuloperoneal Myopathy, X-linked Dominant | Mannosidase Deficiency Diseases | Brachydactyly | Trichorhinophalangeal Syndrome | Alopecia | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Oculocutaneous Albinism Type 2 | Hyperkalemic Periodic Paralysis | Pneumococcal Meningitis | Charcot-Marie-Tooth Disease Type 4D | Generalized Epilepsy With Febrile Seizures Plus | Spinocerebellar Ataxia Type 20 | Hyperuricemia | Adenosine Deaminase Deficiency | Hyperphenylalaninemia | Hepatitis, Alcoholic | Acute Leukemia | Chondrodysplasia Punctata 1, X-linked Recessive | Noonan Syndrome | Amebiasis | Stuve-Wiedemann Syndrome | Hemangioblastoma | Heroin Dependence | Presbyopia | Dominant Optic Atrophy | Gastric Atrophy | Succinic Semialdehyde Dehydrogenase Deficiency | Adult Polyglucosan Body Disease | Non-Langerhans Cell Histiocytosis | Glycogen Storage Disease Type 1a | Blepharitis | Essential Fructosuria | Cryptosporidiosis | Hypotonia-cystinuria Syndrome | Medulloblastoma | Walker-Warburg Syndrome | Avian Influenza | Spitzoid Melanoma | Diffuse Intrinsic Pontine Glioma | Alpha-mannosidosis | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Osteogenesis Imperfecta Type V | Potocki-Shaffer Syndrome | Congenital Poikiloderma | Heart Failure | Sick Sinus Syndrome 1 | Klippel-Feil Syndrome | Focal Segmental Glomerulosclerosis | Left Ventricular Noncompaction | Saul-Wilson Syndrome | Hepatopulmonary Syndrome | Cerebral Cavernous Malformations | Hyperoxaluria | Congenital Hereditary Endothelial Dystrophy Type I | Esthesioneuroblastoma | Malonyl-CoA Decarboxylase Deficiency | Tricho-hepato-enteric Syndrome | Duane Retraction Syndrome | Congenital Muscular Dystrophy | Hypotension, Orthostatic | Cystitis, Interstitial | Polydactyly | Aarskog-Scott Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Patent Ductus Arteriosus | Multisystemic Smooth Muscle Dysfunction Syndrome | Myoclonus-dystonia Syndrome | Cardiospondylocarpofacial Syndrome | Mitochondrial Myopathy | Sjogren Syndrome | Hartnup Disease | Pre-eclampsia | Vestibular Disease | Auriculocondylar Syndrome | Trismus-pseudocamptodactyly Syndrome | Ischemia | Perry Syndrome | Argininosuccinic Aciduria | Vaginitis | Meconium Ileus | C3 Glomerulonephritis | Seminoma | Inflammatory Joint Disease | Brenner Tumor | Melanoma | Light Chain Amyloidosis | Acute Lung Injury | Charcot-Marie-Tooth Disease, Type 2A | Bladder Exstrophy | Autonomic Neuropathy | Progressive Myoclonic Epilepsy | Facioscapulohumeral Muscular Dystrophy Type 1 | Nemaline Myopathy | Androgenic Alopecia | Fragile X Syndrome | Fowler's Syndrome | Keratitis-ichthyosis-deafness Syndrome | Spinocerebellar Ataxia Type 23 | Subacute Sclerosing Panencephalitis | Short-chain Acyl-CoA Dehydrogenase Deficiency | Hemolytic Anemia | Influenza | Ovarian Hyperstimulation Syndrome | Congestive Heart Failure | Retinal Dystrophy, Early-onset Severe | Cold-induced Sweating Syndrome | Chronic Periodontitis | Nephritis, Interstitial | Anorectal Malformations | Giant Cell Arteritis | Colitis, Microscopic | Spasticity | Atherosclerosis | Nicotine Addiction | Hepatic Steatosis | Lipodystrophy | Cabezas Syndrome | Azoospermia | Cerebrotendinous Xanthomatosis | Angioimmunoblastic T-cell Lymphoma | Dengue Shock Syndrome | Gynecomastia | Metabolic Syndrome | Premenstrual Syndrome | Sialidosis Type I | Achondrogenesis | Jacobsen Syndrome | Reticular Dysgenesis | Sclerosteosis 2 | Small Lymphocytic Lymphoma | Spinocerebellar Ataxia Type 7 | Acrodysostosis | Behcet's Disease | Lymphoma | Mucolipidosis Type III | Alzheimer Disease, Late Onset | Renal Failure | Spondyloperipheral Dysplasia | Acute Kidney Injury | Myelofibrosis | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Peeling Skin Syndrome Type B | Clouston Hidrotic Ectodermal Dysplasia | Cholangiocarcinoma | Macular Degeneration | Anorexia Nervosa | Salla Disease | Blepharo-cheilo-odontic Syndrome | Lymphoproliferative Disorders | Nephropathy | Mucolipidosis | Unverricht-Lundborg Syndrome | SAPHO Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Androgen Insensitivity | Chondrosarcoma | Lymphangioleiomyomatosis | Botulism | Myoclonus | Adenoma, Pleomorphic | Hyperparathyroidism, Secondary | Charcot-Marie-Tooth Disease Axonal Type 2N | Congenital Central Hypoventilation Syndrome | Pemphigus Foliaceus | Fibrillation, Atrial | Acanthosis Nigricans | Keratocystic Odontogenic Tumor | Motor Neuron Diseases | Frontotemporal Dementia | Scabies | Birk-Barel Syndrome | Parkinsonism | Proximal Symphalangism | Sleep Apnea, Obstructive | Nasodigitoacoustic Syndrome | Marfan Syndrome | Congenital Heart Defects | Angioedema | Thrombocytopenia | Thymoma, Malignant | Synpolydactyly | Muscular Dystrophy | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Osteoporosis | Neovascular Glaucoma | Glanzmann Thrombasthenia | Mabry Syndrome | Carey-Fineman-Ziter Syndrome | Dysplastic Nevus | Long QT Syndrome Type 1 | HANAC Syndrome | Behavioral Variant Of Frontotemporal Dementia | Microvillus Inclusion Disease | Plasma Cell Dyscrasia | Connective Tissue Disorders | Hypercholesterolemia | Isovaleric Acidemia | Hyperparathyroidism, Primary | Spinocerebellar Ataxia Type 3 | Snyder-Robinson Syndrome | Micro Syndrome | Protein C Deficiency | Tangier Disease | Alpha-1 Antitrypsin Deficiency | Granular Corneal Dystrophy Type 1 | Juvenile Xanthogranuloma | Distal Myopathy | Ectopia Lentis, Isolated, Autosomal Recessive | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Myosin Storage Myopathy | Seborrheic Dermatitis | Acute Lymphocytic Leukemia | Graves Disease | Reflex Epilepsy | Werner's Syndrome | Beare-Stevenson Syndrome | Hypertension, Renovascular | Craniolenticulosutural Dysplasia | Malignant Peripheral Nerve Sheath Tumor | Tonsillitis | Neurofibromatosis | Proteus Syndrome | Dermatomyositis | Sarcoidosis, Pulmonary | Ureteropelvic Junction Obstruction | MIRAGE Syndrome | Vici Syndrome | Hydrolethalus Syndrome | Acrocallosal Syndrome | Hereditary Hemorrhagic Telangiectasia | Diabetes Insipidus | Pouchitis | Hereditary Neuropathy With Liability To Pressure Palsies | Infantile Neuroaxonal Dystrophy | Epiphyseal Chondrodysplasia, Miura Type | Asperger Syndrome | Pilomatrix Carcinoma | Bethlem Myopathy | Neuromyotonia | Hyperammonemia | Neuroblastoma | HUPRA Syndrome | Leukoplakia, Oral | Chiari Malformation Type I | Rhabdomyosarcoma | Neurofibromatosis-Noonan Syndrome | Dengue Hemorrhagic Fever | Postaxial Polydactyly | Cardiomyopathy, Peripartum | Ocular Albinism Type 1 | Agranulocytosis | Arthritis, Reactive | Chronic Inflammatory Demyelinating Polyneuropathy | Spermatocele | Hennekam Lymphangiectasia-lymphedema Syndrome | Lathosterolosis | Lentigo | Encephalitis, Tick-borne | Neonatal Progeroid Syndrome | Macular Corneal Dystrophy | Hereditary Mixed Polyposis Syndrome | Waardenburg Syndrome Type 2 | Aspergillosis | Polymyositis | Atopy | Thyroid Hormone Resistance | Lupus Erythematosus | Epidermolysis Bullosa Simplex, Localized | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Muscle Wasting | Vitreoretinal Degeneration, Snowflake Type | Epidermal Nevus Syndrome | Dysthymia | Hyperthermia, Malignant | Peroxisomal Disorder | Hemangioma | Sezary Syndrome | Keratoconjunctivitis | Hypoproteinemia, Hypercatabolic | Peters-plus Syndrome | Cole-Carpenter Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Epilepsy, Generalized | Sertoli Cell-only Syndrome | Nanophthalmos | MELAS Syndrome | Herpes Simplex Dermatitis | Acromesomelic Dysplasia | Papilloma | Paracoccidioidomycosis | Glaucoma, Congenital | Histoplasmosis | Epidermolysis Bullosa | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Peritonitis | Measles