Disease

VACTERL/VATER Association

About the Disease
Vater/vacterl Association, also known as vacterl association, is related to vacterl association, x-linked, with or without hydrocephalus and vacterl association with hydrocephalus. An important gene associated with Vater/vacterl Association is HOXD13 (Homeobox D13). The drugs Nicotinamide and Niacin have been mentioned in the context of this disorder. Affiliated tissues include kidney, pancreas and heart, and related phenotypes are anal atresia and polyhydramnios

Common Targets
NADSYN1

疾病靶点研报
VACTERL/VATER Association

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

Other Diseases

Lateral Meningocele Syndrome | Mood Disorder | Down Syndrome | Irritable Bowel Syndrome | Glioblastoma Multiforme | Riboflavin Transporter Deficiency Neuronopathy | Hereditary Mixed Polyposis Syndrome | Sensory Neuropathy | Epidermodysplasia Verruciformis | Dubin-Johnson Syndrome | Tylosis With Esophageal Cancer | Periventricular Nodular Heterotopia | Lactose Intolerance | Acquired Partial Lipodystrophy | Nemaline Myopathy 8 | Loeys-Dietz Syndrome | Aspergillosis | Pheochromocytoma | Gangliosidosis | Premature Ejaculation | Goldenhar Syndrome | Thyroiditis, Autoimmune | Fibronectin Glomerulopathy | Muir-Torre Syndrome | Wieacker-Wolff Syndrome | Pneumonia, Mycoplasma | Diabetes Type 1 | Adenoid Cystic Carcinoma | Enlarged Vestibular Aqueduct | Lafora Disease | Arteriovenous Malformations | Vitamin B12 Deficiency | Episodic Ataxia Type 1 | Rosacea | Inflammatory Myofibroblastic Tumor | Neovascular Glaucoma | Osteopathia Striata With Cranial Sclerosis | Gaucher Disease | VACTERL/VATER Association | Charcot-Marie-Tooth Disease | Autosomal Recessive Bestrophinopathy | Lymphopenia | Chitayat Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Cancer, Bladder | Acute Myeloid Leukemia | Bronchiectasis | Alopecia Totalis | Hairy Cell Leukemia | Congenital Dysfibrinogenemia | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Small Lymphocytic Lymphoma | Subcortical Band Heterotopia | Corneal Ulcer | Spondylosis | Ichthyosis | Trichothiodystrophy | Retinoschisis | Mevalonate Kinase Deficiency | Alcoholism | Delayed Sleep Phase Syndrome | Colitis, Collagenous | Epidermolytic Ichthyosis, Annular | Glycogen Storage Disease Type 5 | Duodenal Atresia | Osteomalacia | Progressive External Ophthalmoplegia | Premenstrual Syndrome | Spinal Muscular Atrophy | Charcot-Marie-Tooth Disease, Type 2C | Primary Hyperoxaluria Type 3 | Poikiloderma With Neutropenia | Myosin Storage Myopathy | Coenzyme Q10 Deficiency | Galactosialidosis | Spondylo-ocular Syndrome | Cornelia De Lange Syndrome | Vitelliform Macular Dystrophy | Intermittent Explosive Disorder | Varicocele | Neurogenic Bladder | Hidradenitis Suppurativa | Asthma, Nocturnal | Hyperhomocysteinemia | Postpoliomyelitis Syndrome | Pseudohypoaldosteronism | Congenital Dyserythropoietic Anemia | Raine Syndrome | Holt-Oram Syndrome | Chorioretinitis | Generalized Epilepsy And Paroxysmal Dyskinesia | Carney-Stratakis Syndrome | Agranulocytosis | Lipid Storage Diseases | Primary Lateral Sclerosis | Sick Sinus Syndrome 1 | Oculocutaneous Albinism Type 2 | Familial Hemiplegic Migraine | Sialoadenitis | Aceruloplasminemia | Uveitis, Anterior | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Central Core Disease | Takenouchi-Kosaki Syndrome | Pancreatitis, Chronic | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Sialidosis Type I | Rothmund-Thomson Syndrome | Hermansky-Pudlak Syndrome | Heterotopic Ossification | Cluster Headache | Benign Familial Infantile Seizures | Feingold Syndrome | Cyclic Vomiting Syndrome | Congenital Hemolytic Anemia | Perry Syndrome | Neonatal Progeroid Syndrome | Fuchs Dystrophy | Glaucomatocyclitic Crisis | Agnathia-Otocephaly Complex | Osteosarcoma | Photosensitivity | Keratosis, Seborrheic | Ataxia-ocular Apraxia 2 | Porphyria Cutanea Tarda | Cryopyrin-associated Periodic Syndromes | Cardiomyopathy, Restrictive | Blastoma, Pleuropulmonary | Globozoospermia | Autosomal Recessive Spastic Paraplegia Type 75 | Gilbert Syndrome | Encephalopathy | Arthritis, Psoriatic | Albinism | Occipital Neuralgia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Spinocerebellar Ataxia Type 10 | Carcinoma, Squamous Cell | Spinal Muscular Atrophy Type 3 | Huntington's Disease-like 2 | Dysgerminoma | Camptocormia | GLUT1 Deficiency Syndrome | Synpolydactyly | Ganglioglioma | Keratopathy | Tatton-Brown-Rahman Syndrome | Hemolytic Uremic Syndrome, Atypical | Schwannoma | Lattice Corneal Dystrophy Type 1 | Gliosarcoma | Osteochondrosis | Progressive Familial Intrahepatic Cholestasis | Prostatitis | Hyperbilirubinemia | Hypercalcemia | Anxiety Disorders | Gray Platelet Syndrome | Castleman Disease | Osteogenesis Imperfecta | Myopathy | Familial Glucocorticoid Deficiency | Genitopatellar Syndrome | Neuromyotonia | Osteochondroma | Congenital Diaphragmatic Hernia | Chromosome 16p11.2 Deletion Syndrome | Agoraphobia | Hypoproteinemia, Hypercatabolic | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Dystonia | Galactosemia | Hypermethioninemia | Phosphoglycerate Dehydrogenase Deficiency | Molybdenum Cofactor Deficiency | Renal Dysplasia | Narcolepsy | Congestive Heart Failure | Acrocallosal Syndrome | Renal Oncocytoma | Oligodendroglioma | Mucormycosis | Dementia, Vascular | Congenital Nystagmus | Cat Eye Syndrome | Non-small Cell Lung Cancer | Osteonecrosis Of The Jaw | Vogt-Koyanagi-Harada Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | Carcinoma, Signet Ring Cell | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Giant Axonal Neuropathy | Lymphoma | Waardenburg Syndrome | Brenner Tumor | Lymphangioma | Congenital Hereditary Endothelial Dystrophy Type I | Dermatomyositis | Glaucoma, Congenital | Heavy Chain Disease | Goiter | Mitochondrial Cytopathy | Carcinoma, Merkel Cell | HIBCH Deficiency | Neurofibromatosis-Noonan Syndrome | Retinitis Pigmentosa 3 | Maternally Inherited Diabetes And Deafness | Acromicric Dysplasia | Spinocerebellar Ataxia Type 38 | Diabetic Encephalopathy | Congenital Sodium Diarrhea | Ehlers-Danlos Syndrome | Tenosynovial Giant Cell Tumor | Spondylocostal Dysostosis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Tay-Sachs Disease | Charcot-Marie-Tooth Disease Type 2T | Mast Cell Leukemia | Spinocerebellar Ataxia Type 31 | Benign Familial Pemphigus | Vertebrobasilar Insufficiency | Angioedema | Adenocarcinoma | Platelet Disorders | Cardiac Sarcoidosis | Holoprosencephaly | Retinopathy Of Prematurity | Focal Facial Dermal Dysplasia | Binge Eating Disorder | Glutaric Aciduria Type 3 | Hyperoxaluria | Kaposi Sarcoma | Glycogen Storage Disease Type 0 | Aicardi-Goutieres Syndrome | Recurrent Respiratory Papillomatosis | Hypertension | Osteomyelitis | Cold Agglutinin Disease | 3-methylglutaconic Aciduria Type IV | Macrophagic Myofasciitis | Myeloid Leukemia | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Spinocerebellar Ataxia Type 15 | Hypophosphatasia | Hepatic Steatosis | Warsaw Breakage Syndrome | Polycystic Kidney, Autosomal Recessive | Spondylometaphyseal Dysplasia | Alopecia | Adrenomyeloneuropathy | Cardiofaciocutaneous Syndrome | Cantu Syndrome | Peripheral Neuropathy | Scabies | Omenn Syndrome | Insulin Resistance | Cold-induced Sweating Syndrome | Pregnancy, Ectopic | Pain | Intestinal Hypomagnesemia 1 | Meleda Disease | Pompe Disease | Parkinsonism | Patent Foramen Ovale | Leigh Syndrome | Autoimmune Autonomic Ganglionopathy | Schuurs-Hoeijmakers Syndrome | Metachromatic Leukodystrophy | Primary Progressive Aphasia | Deafness, Dystonia, And Cerebral Hypomyelination | Lassa Fever | Reflex Epilepsy | Left Ventricular Noncompaction | Progressive Encephalopathy-optic Atrophy Syndrome | Gastroenteritis | Dermatitis | Gastrointestinal Disorders | Majeed Syndrome | Connective Tissue Disorders | Filariasis | Impulse Control Disorder | Antenatal Bartter Syndrome Type 1 | Partington Syndrome | Epilepsy | Diverticulitis | Corneal Dystrophy And Perceptive Deafness | Sertoli Cell-only Syndrome | Anorchia | Acute Anterior Uveitis | Spinal Cord Diseases | Acute Motor Axonal Neuropathy | Epidermal Nevus Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Hypercholesterolemia, Familial | Pancreatitis | Pneumothorax | Adenoma, Pituitary | Astrocytoma | Myelitis, Transverse | Vasculitis | Tyrosinemia Type 2 | Chondrodysplasia Punctata 1, X-linked Recessive | Peroxisomal Disorder | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Thalassemia, Beta | Chondrosarcoma | Spinocerebellar Ataxia Type 28 | Ocular Albinism Type 1 | Macular Corneal Dystrophy | Hydronephrosis | Microcephaly, Seizures, And Developmental Delay | Progressive Osseous Heteroplasia | Alagille Syndrome | Meningitis | Acute Lung Injury | Episodic Ataxia | Asthma | Waardenburg Syndrome Type 2E | Fetal And Neonatal Alloimmune Thrombocytopenia | Kabuki Syndrome 2 | Hypertension, Renal | Otosclerosis | Gastritis, Atrophic | COACH Syndrome | Pemphigus Vulgaris | Lipodystrophy | Mitochondrial DNA Depletion Syndrome | Lesch-Nyhan Syndrome | Hemochromatosis | Multisystemic Smooth Muscle Dysfunction Syndrome | Hereditary Coproporphyria | Familial Episodic Pain Syndrome | X-linked Creatine Transporter Deficiency | Spina Bifida | Diabetes Insipidus, Neurogenic | Vici Syndrome | Pseudomyxoma Peritonei | Arteriosclerosis | Brugada Syndrome 1 | Crisponi Syndrome | Neuroendocrine Cancer | GM2-gangliosidosis AB Variant | Benign Recurrent Intrahepatic Cholestasis 1 | Myotonic Disorders | Vitreoretinal Degeneration, Snowflake Type | Large Granular Lymphocytic Leukemia | Pilomatrix Carcinoma | Sclerocornea | Cervicitis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Spondyloarthritis | Waardenburg Syndrome Type 4 | Encephalitis, Tick-borne | Coronary Restenosis | Chronic Lymphocytic Leukemia | Knobloch Syndrome | Trichuriasis | Imerslund-Grasbeck Syndrome | Multiple System Atrophy | Alzheimer Disease, Late Onset | Neurocysticercosis | Lymphoma, AIDS-related | Osteoporosis, Postmenopausal | Rhabdomyosarcoma, Alveolar | Melanocytic Nevus | Sickle Cell Anemia | Cranioectodermal Dysplasia | Early Infantile Epileptic Encephalopathy 4 | Norrie Disease | Leiomyoma | Nestor-Guillermo Progeria Syndrome | Jacobsen Syndrome | Plasma Cell Leukemia | Hereditary Inclusion Body Myopathy | Corticobasal Syndrome | Aneurysm, Thoracic Aortic | Poretti-Boltshauser Syndrome | Pseudoexfoliation Syndrome | Motor Neuron Diseases | Nager Acrofacial Dysostosis | Trismus-pseudocamptodactyly Syndrome | DRESS Syndrome | NDH Syndrome | Van Der Knaap Disease | Costello Syndrome | Lipoma | Lathosterolosis | Thrombosis | Proteasome-associated Autoinflammatory Syndrome 2 | Chronic Kidney Disease | Osteogenesis Imperfecta Type III | Osteoglophonic Dysplasia | Paraganglioma, Carotid Body | Hyperacusis | Follicular Dendritic Cell Sarcoma | Schwartz-Jampel-Aberfeld Syndrome | Congenital Bile Acid Synthesis Defect | Intellectual Disability, Autosomal Dominant 5 | Gyrate Atrophy Of The Choroid And Retina | Hypotension, Orthostatic