Disease

X-linked Acrogigantism

About the Disease
Chromosome Xq26.3 Duplication Syndrome, also known as x-linked acrogigantism, is related to lissencephaly, x-linked, 2 and acromegaly, and has symptoms including snoring and thick skin. An important gene associated with Chromosome Xq26.3 Duplication Syndrome is CXDUPQ26.3 (Chromosome Xq26.3 Duplication Syndrome). Affiliated tissues include pituitary, hypothalamus and skin, and related phenotypes are tall stature and increased circulating prolactin concentration

Common Targets
IFT140

疾病靶点研报
X-linked acrogigantism

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

Other Diseases

Sialidosis | Ellis-Van Creveld Syndrome | Nephrotic Syndrome | Neurocutaneous Melanocytosis | Sarcoidosis | Porphyria, Acute Intermittent | Dyslexia | Turner's Syndrome | Waardenburg Syndrome Type 2 | Hereditary Hemorrhagic Telangiectasia Type 2 | Herpes Genitalis | Thalassemia, Beta | Stevens-Johnson Syndrome | Neurogenic Bladder | Sclerosteosis 2 | Arteriosclerosis | Tibial Muscular Dystrophy | Thyroiditis | Hereditary Mixed Polyposis Syndrome | Bronchitis, Chronic | Metatropic Dysplasia | Adenoid Cystic Carcinoma | Paget's Disease Of The Breast | TARP Syndrome | Heroin Dependence | Epidermodysplasia Verruciformis | Histiocytic Sarcoma | DRESS Syndrome | Lassa Fever | Myasthenia Gravis | Colitis, Collagenous | Warsaw Breakage Syndrome | Sertoli Cell-only Syndrome | Dent Disease | Ichthyosis, X-linked | Iron Overload | Low Tension Glaucoma | Heart Failure | Gastric Atrophy | Guanidinoacetate Methyltransferase Deficiency | Neuroendocrine Cancer | Exocrine Pancreatic Insufficiency | Myoclonic Atonic Epilepsy | Chondromyxoid Fibroma | Nail Disorder, Nonsyndromic Congenital | Waardenburg Syndrome Type 1 | Porencephaly | Dermatitis Herpetiformis | Diffuse Palmoplantar Keratoderma | Malaria | Congenital Poikiloderma | Motion Sickness | Primary Sclerosing Cholangitis | Epidermolysis Bullosa Acquisita | Eclampsia | Glomerulonephritis, Membranous | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Familial Hemiplegic Migraine | Heterotopic Ossification | Hairy Cell Leukemia | Rheumatoid Arthritis | Enlarged Vestibular Aqueduct | Craniosynostosis | H Syndrome | AIDS Dementia Complex | Angioedema, Hereditary | Epidermolytic Hyperkeratosis | Hypermethioninemia | Osteosclerosis | Wolff-Parkinson-White Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Osteoarthritis | Skin Fragility-woolly Hair Syndrome | Spondylometaphyseal Dysplasia | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Angiodysplasia | Dysfibrinogenemia | Dermatofibrosarcoma | Amyotrophic Lateral Sclerosis | Nevus | Glycogen Storage Disease Type 1a | Charcot-Marie-Tooth Disease, Type 2A | Angiosarcoma | Renal-hepatic-pancreatic Dysplasia | Adenomyosis | Spinocerebellar Ataxia Type 8 | Colitis | Subacute Sclerosing Panencephalitis | Acute Anterior Uveitis | Swine Influenza | Skin Papilloma | Neovascular Glaucoma | Myhre Syndrome | Congenital Bile Acid Synthesis Defect | Porokeratosis | Sponastrime Dysplasia | Borjeson-Forssman-Lehmann Syndrome | Brugada Syndrome 1 | Lysosomal Acid Lipase Deficiency | Retinal Degeneration | Smith-Lemli-Opitz Syndrome | HELLP Syndrome | Von Hippel-Lindau Disease | Eiken Syndrome | Cirrhosis | Thanatophoric Dysplasia | Brachial Plexus Neuropathy | Birk-Barel Syndrome | Focal Facial Dermal Dysplasia | Creatine Deficiency Syndrome | Focal Cortical Dysplasia Type 2 | GATA2 Deficiency | Traboulsi Syndrome | Duane Retraction Syndrome | Angioimmunoblastic T-cell Lymphoma | Meningitis | Oculocutaneous Albinism Type 2 | Congenital Tufting Enteropathy | Gliosarcoma | Uterine Leiomyoma | Pemphigus | Cystitis, Interstitial | Neurofibromatosis | Poikiloderma With Neutropenia | Larsen Syndrome | Bare Lymphocyte Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Androgen Insensitivity | Cherubism | Polydactyly | VEXAS Syndrome | Niemann-Pick Disease, Type B | Triple A Syndrome | Kernicterus | Gardner Syndrome | Agammaglobulinemia | Oculocutaneous Albinism Type 4 | Retinitis Pigmentosa 3 | Brenner Tumor | Cantu Syndrome | Duodenal Atresia | Shock, Cardiogenic | Torticollis | Gastrointestinal Disorders | Intellectual Disability, Autosomal Dominant 5 | Pterygium | Diamond-Blackfan Anemia | Polyarteritis Nodosa | Seizures | Glomerulonephritis | Cri-du-chat Syndrome | Fetal Alcohol Syndrome | Pernicious Anemia | Norrie Disease | Non-Langerhans Cell Histiocytosis | Lewy Body Dementia | Malnutrition | Amblyopia | Dengue Shock Syndrome | Chordoid Glioma | Microtia | Peeling Skin Syndrome Type B | Postpartum Depression | 3-M Syndrome | Erythema Multiforme | Diffuse Mesangial Sclerosis | Xeroderma Pigmentosum Variant Type | Acute Myeloid Leukemia | Primrose Syndrome | Diverticulitis | Mucolipidosis Type III | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Leiomyosarcoma | Benign Familial Neonatal Convulsions | Anorectal Fistula | Odonto-onycho-dermal Dysplasia | Multifocal Motor Neuropathy | Infertility, Male | Ophthalmoplegia | Chondrodysplasia Punctata 1, X-linked Recessive | Ectodermal Dysplasia | Tardive Dyskinesia | Congenital Dyserythropoietic Anemia | Schwartz-Jampel-Aberfeld Syndrome | Chordoma | GM2-gangliosidosis AB Variant | Protein S Deficiency | Growth Hormone Excess | Hepatitis, Autoimmune | Enterocolitis, Necrotizing | Peters-plus Syndrome | Sensorineural Hearing Loss | Pseudomyxoma Peritonei | Pyruvate Decarboxylase Deficiency | Blastoma, Pleuropulmonary | Premenstrual Syndrome | Alcoholism | Mitochondrial DNA Depletion Syndrome | Dysferlinopathy | Cataract | Craniofacial Dysostosis | Van Der Knaap Disease | Pontocerebellar Hypoplasia Type 2 | Hereditary Elliptocytosis | Mucolipidosis Type IV | Brooke-Spiegler Syndrome | Peutz-Jeghers Syndrome | X-linked Charcot-Marie-Tooth Disease | Hennekam Lymphangiectasia-lymphedema Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Hemangioma | Congenital Stromal Corneal Dystrophy | Hemimegalencephaly | Varices | X-linked Acrogigantism | Dengue Hemorrhagic Fever | Williams Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | PASLI Disease | Antenatal Bartter Syndrome Type 1 | Niemann-Pick Disease, Type C | Transthyretin-related Amyloidosis | Measles | Coma | 5-oxoprolinase Deficiency | Idiopathic Pulmonary Fibrosis | Herpes Simplex Dermatitis | Pseudohypoaldosteronism | Vogt-Koyanagi-Harada Syndrome | Hydronephrosis | ADNP Syndrome | FG Syndrome | Asthma, Nocturnal | Pleomorphic Xanthoastrocytoma | Gangliosidosis | Autosomal Recessive Spastic Paraplegia Type 35 | Fukuyama Congenital Muscular Dystrophy | Galloway-Mowat Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Chanarin-Dorfman Syndrome | Goldenhar Syndrome | Heart Block | Thromboembolism | Acute Chest Syndrome | Cardiomyopathy, Dilated, 1L | Oculocutaneous Albinism Type 1 | Toxoplasmosis | Hypospadias | Familial Cerebral Amyloid Angiopathy | Aneurysm, Abdominal Aortic | Central Pain Syndrome | L-2-Hydroxyglutaric Aciduria | Giant Cell Glioblastoma | Krabbe Disease | Phosphoglycerate Dehydrogenase Deficiency | Glutathione Synthetase Deficiency | Gnathodiaphyseal Dysplasia | Down Syndrome | Esophageal Adenocarcinoma | Adrenal Insufficiency | Sarcosinemia | Gigantism | Congenital Generalized Lipodystrophy | Epicondylitis | Pneumoconiosis | T-cell Chronic Lymphocytic Leukemia | Keratopathy | Metachondromatosis | Charcot-Marie-Tooth Disease, Type 1A | Schizencephaly | Fuchs Dystrophy | Left Ventricular Noncompaction | Erythematotelangiectatic Rosacea | Connective Tissue Disorders | Agnathia-Otocephaly Complex | Liddle Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Dysplastic Nevus | Congenital Heart Block | Ocular Hypertension | Retinal Telangiectasia | Angioedema, Acquired | Scoliosis | Retinal Detachment | Bardet-Biedl Syndrome | Ocular Albinism Type 1 | Succinic Semialdehyde Dehydrogenase Deficiency | Benign Hereditary Chorea | Keratoacanthoma | Headache | Sleep Apnea, Central | Hemorrhoids | Alpha-mannosidosis | Hyperferritinemia-cataract Syndrome | Atrioventricular Septal Defect | Myotonic Disorders | Chronic Idiopathic Myelofibrosis | Iron Metabolism Disorders | Cluster Headache | Moyamoya Disease | Epidermolysis Bullosa Simplex, Generalized | Charcot-Marie-Tooth Disease Type 4E | Glycogen Storage Disease Type 1b | Alopecia Areata | Retinopathy, Diabetic | Hyperkalemic Periodic Paralysis | Hereditary Sensory Neuropathy Type 1 | Congenital Myasthenic Syndrome | Toxic Epidermal Necrolysis | Gastritis, Atrophic | Miyoshi Myopathy | Inflammatory Linear Verrucous Epidermal Nevus | Epidermolysis Bullosa | Apert Syndrome | Diabetes Type 2 | Neurodegeneration With Brain Iron Accumulation | Glioblastoma Multiforme | Central Core Disease | Spinocerebellar Ataxia Type 40 | Lipoma | Dermatomyositis | Infantile Spasm | Seasonal Mood Disorder | Tangier Disease | Supravalvular Aortic Stenosis | Bone Giant Cell Tumor | Becker Muscular Dystrophy | Esotropia | Fabry's Disease | Primary Carnitine Deficiency | Epidermolytic Ichthyosis, Annular | Epidermolytic Palmoplantar Keratoderma | Posterior Polar Cataract | Optic Neuritis | Cole-Carpenter Syndrome | Perry Syndrome | Oculopharyngeal Muscular Dystrophy | Chudley-McCullough Syndrome | Glioma | Acute Motor Axonal Neuropathy | Vitelliform Macular Dystrophy | Varicocele | Progressive External Ophthalmoplegia | Idiopathic Multicentric Castleman Disease | Sweet Syndrome | Spinocerebellar Ataxia Type 6 | Lymphoma, B-cell | Hepatitis A | Osteogenesis Imperfecta | Glioblastoma | Hyperbilirubinemia | Thalassemia | Sarcoidosis, Pulmonary | Congenital Adrenal Hyperplasia | Hyperoxaluria | Alstrom Syndrome | Neurofibromatosis Type 2 | Myositis | Myoclonus-dystonia Syndrome | Leukoencephalopathy, Progressive Multifocal | Ollier Disease | T-cell Lymphoma, Subcutaneous Panniculitis-like | HUPRA Syndrome | Primary Cutaneous Amyloidosis | Coffin-Lowry Syndrome | Echinococcosis | Acrocallosal Syndrome | Hypotonia-cystinuria Syndrome | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Hyperostosis | Tuberculous Meningitis | Raine Syndrome | Wagner Disease | Cold-induced Sweating Syndrome | DICER1 Syndrome | Spinocerebellar Ataxia Type 20 | Hypothalamic Obesity | Eccrine Porocarcinoma | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Alzheimer Disease, Late Onset | Diabetic Neuropathy | Campomelic Dysplasia | Pituitary Stalk Interruption Syndrome | Fibromyalgia | Charcot-Marie-Tooth Disease Type 2T | Ectopia Lentis, Isolated, Autosomal Recessive | Olmsted Syndrome | Kindler Syndrome | Liver Diseases | Pseudohypoparathyroidism Type 1A | Priapism | Osteopathia Striata With Cranial Sclerosis | Senior-Loken Syndrome | Glomerulonephritis, Membranoproliferative | Burn-McKeown Syndrome | Spinal And Bulbar Muscular Atrophy | Angiomyolipoma | Meningococcal Infections | Galactosialidosis