ADNP Syndrome

About the Disease
Helsmoortel-Van Der Aa Syndrome, also known as hvdas, is related to ohdo syndrome and autism spectrum disorder. An important gene associated with Helsmoortel-Van Der Aa Syndrome is ADNP (Activity Dependent Neuroprotector Homeobox), and among its related pathways/superpathways are Chromatin organization and Chromatin Regulation / Acetylation. The drugs Ketamine and Anesthetics, Intravenous have been mentioned in the context of this disorder. Affiliated tissues include heart, brain and eye, and related phenotypes are delayed speech and language development and urinary incontinence

Common Targets
ADNP | Neurotrophic Factor (nonspecified subtype)

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

Other Diseases

Oculopharyngeal Muscular Dystrophy | Reticular Dysgenesis | Sporadic Hemiplegic Migraine | Thymoma, Malignant | Carcinoma In Situ | Joubert Syndrome | Alopecia Totalis | Focal Cortical Dysplasia Type 2 | Progressive Encephalopathy-optic Atrophy Syndrome | Centronuclear Myopathy | Facioscapulohumeral Muscular Dystrophy | Amebiasis | Uremia | Multiple Sulfatase Deficiency | C3 Glomerulopathy | CREST Syndrome | Anosmia, Congenital | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Cherubism | Atherosclerosis | Christianson Syndrome | Familial Partial Lipodystrophy | Vitamin K Deficiency | Trimethylaminuria | Charcot-Marie-Tooth Disease, Type 2C | Congenital Sodium Diarrhea | Diabetes Insipidus, Nephrogenic | Cataplexy | Sick Sinus Syndrome | Mucolipidosis | Norrie Disease | Polyarteritis Nodosa | Spinocerebellar Ataxia Type 10 | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Arrhythmogenic Right Ventricular Cardiomyopathy | Primary Sclerosing Cholangitis | Dominant Optic Atrophy | Hypersensitivity | Malignant Peripheral Nerve Sheath Tumor | Amenorrhea | Transcobalamin Deficiency | Renal Dysplasia | Enhanced S-cone Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Smoldering Myeloma | Spinocerebellar Ataxia Type 27 | Episodic Ataxia | Localized Scleroderma | Familial Glucocorticoid Deficiency | Dystonia Musculorum Deformans | Congenital Heart Defects | Huntington's Disease | Osteogenesis Imperfecta Type IV | Glioblastoma Multiforme | Tendinitis | Nemaline Myopathy 10 | Lentigo | Diastrophic Dysplasia | Bronchitis, Chronic | Yellow Fever | Nephroblastoma | Asthma, Exercise-induced | Arthritis, Psoriatic | Coronary Artery Disease | Carotid Artery Disease | Syndactyly | Becker Muscular Dystrophy | Alkaptonuria | Kallmann Syndrome | Dermatomyositis | Congenital Hereditary Endothelial Dystrophy Type I | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Sezary Syndrome | Neuromyelitis Optica | Osteonecrosis Of The Jaw | Retinopathy Of Prematurity | Cutaneous Lupus Erythematosus | Adult Polyglucosan Body Disease | PHARC Syndrome | Rheumatic Heart Disease | Leishmaniasis, Visceral | Carbamoyl Phosphate Synthetase I Deficiency | Crigler-Najjar Syndrome | Intracerebral Hemorrhage | Restrictive Dermopathy | Isobutyryl-CoA Dehydrogenase Deficiency | Zimmermann-Laband Syndrome | Usher Syndrome | Diabetic Encephalopathy | Leprosy | Myofibrillar Myopathy | Thyroid Dyshormonogenesis | Obesity, Morbid | Cat Eye Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Hepatoblastoma | Acute Tubular Necrosis | Primary Hyperoxaluria Type 3 | Epidermodysplasia Verruciformis | Hernia, Inguinal | Sweet Syndrome | Perivascular Epithelioid Cell Tumor | Lymphangioma | Ollier Disease | Progressive Osseous Heteroplasia | Hypertension, Essential | Supravalvular Aortic Stenosis | Gray Platelet Syndrome | Ocular Surface Squamous Neoplasia | Enlarged Vestibular Aqueduct | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Tetraplegia | Pulmonary Alveolar Proteinosis | Genitopatellar Syndrome | Craniosynostosis | Oculocutaneous Albinism Type 1 | Pulmonary Veno-occlusive Disease | Conn Syndrome | Depression | CEDNIK Syndrome | Hypermethioninemia | Familial Advanced Sleep Phase Syndrome | Spinocerebellar Ataxia Type 20 | Cholangitis | Basal Ganglia Cerebrovascular Disease | Thyroiditis, Autoimmune | Acute Anterior Uveitis | Androgen Insensitivity | Behavioral Variant Of Frontotemporal Dementia | Hypersensitivity Pneumonitis | Proctitis | Glycogen Storage Disease Type 4 | Neonatal Progeroid Syndrome | Plasma Cell Dyscrasia | Richter's Syndrome | Leukoplakia, Oral | Hypercalciuria | Hartnup Disease | Multiple Epiphyseal Dysplasia | MELAS Syndrome | Coronary Heart Disease | Thrombasthenia | Carney Triad | Pleurisy | Infantile Liver Failure Syndrome 1 | Congestive Heart Failure | Spinocerebellar Ataxia Type 23 | Duchenne Muscular Dystrophy | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Chondromyxoid Fibroma | Hypertrophy | Chronic Mucocutaneous Candidiasis | Superficial Spreading Melanoma | Systemic Mastocytosis | Anovulation | Familial Dysautonomia | X-linked Charcot-Marie-Tooth Disease | Acanthosis Nigricans | Nephrosclerosis | Essential Fructosuria | Transient Bullous Dermolysis Of The Newborn | Hepatitis A | Acute Myeloid Leukemia | Progressive Myoclonic Epilepsy | Peutz-Jeghers Syndrome | Tyrosinemia Type 2 | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Fraser Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Leigh Syndrome | CHOPS Syndrome | Campomelic Dysplasia | Schizophrenia, Paranoid | Fucosidosis | Thyroid Dysgenesis | Systemic Lupus Erythematosus | Endometrial Hyperplasia | Hereditary Inclusion Body Myopathy | Acromegaly | Retinal Dystrophy, Early-onset Severe | Delayed Sleep Phase Syndrome | Hyperlipidemia, Familial Combined | LEOPARD Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Inflammatory Linear Verrucous Epidermal Nevus | Irritable Bowel Syndrome | Gingivitis | Pituitary Dwarfism | Portal Vein Thrombosis | Schnitzler Syndrome | Osteopetrosis | Acute Chest Syndrome | Congenital Primary Aphakia | Cardiomyopathy, Peripartum | Graves Disease | MIRAGE Syndrome | Iron Overload | Best Macular Dystrophy | Carcinoma, Signet Ring Cell | Ichthyosis | Frontometaphyseal Dysplasia | Conjunctivitis | Hyperthermia, Malignant | Congenital Stromal Corneal Dystrophy | Cellulitis | Apert Syndrome | Plasmacytoma | Pheochromocytoma | Carcinoma, Merkel Cell | Coloboma | Corticobasal Syndrome | Coma | Congenital Torticollis | Hepatorenal Syndrome | Angioedema, Acquired | Fontaine Progeroid Syndrome | Tricho-hepato-enteric Syndrome | Acral Lentiginous Melanoma | Nasodigitoacoustic Syndrome | Lymphoma Lymphoblastic | Chronic Periodontitis | Achondrogenesis | Adenomyosis | Micro Syndrome | Burn-McKeown Syndrome | Spinocerebellar Ataxia Type 21 | Jawad Syndrome | Veno-occlusive Disease | Greig Cephalopolysyndactyly Syndrome | Spondylosis | Heimler Syndrome | Pontocerebellar Hypoplasia Type 2 | Hypopigmentation | Progressive Familial Intrahepatic Cholestasis Type 2 | Saul-Wilson Syndrome | Cushing Syndrome | Epidermolysis Bullosa Dystrophica | Membranous Nephropathy | Nephropathy | Hyperinsulinemic Hypoglycemia | Globozoospermia | Multiple Sclerosis, Relapsing-remitting | Mitochondrial Myopathy | Genee-Wiedemann Syndrome | Ebstein Anomaly | Babesiosis | Pulmonary Sclerosing Hemangioma | Sialoadenitis | Prediabetes | Pitt-Hopkins Syndrome | Neurofibroma, Plexiform | Thromboembolism | Arts Syndrome | Fetal Akinesia Deformation Sequence | Carcinoma, Squamous Cell | Inflammatory Joint Disease | Choroiditis | Noonan Syndrome-like Disorder With Loose Anagen Hair | Pearson Syndrome | Birt-Hogg-Dube Syndrome | Astigmatism | Myelodysplasia | CDKL5 Deficiency Disorder | Epilepsy, Generalized | Cardiomyopathy, Hypertrophic | Pulmonary Tuberculosis | Spermatocele | Sleep Apnea, Central | Brachydactyly | Dementia, Vascular | Avian Influenza | Cutaneous Angiosarcoma | Gastritis, Atrophic | Trichuriasis | Thalassemia | Demyelinating Diseases | Hypoglycemia | Tinea | CHARGE Syndrome | Idiopathic Pulmonary Fibrosis | Hyperacusis | 3-methylglutaconic Aciduria Type IV | Spinocerebellar Ataxia Type 7 | Neuropathy | Argininosuccinic Aciduria | Hemolytic Anemia | Nager Acrofacial Dysostosis | Brenner Tumor | Xeroderma Pigmentosum Variant Type | Adams-Oliver Syndrome | Hypohidrotic Ectodermal Dysplasia, X-linked | Congenital Nystagmus | Sulfite Oxidase Deficiency | Hemolytic Uremic Syndrome | Angelman Syndrome | Birk-Barel Syndrome | Polymicrogyria | GLUT1 Deficiency Syndrome | Polycystic Liver | Chloridorrhea, Congenital | Cutaneous Mastocytosis | Leukodystrophies | Encephalitis, Tick-borne | Melanocytic Nevus | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Varicocele | Retinitis Pigmentosa 3 | Blau Syndrome | Majeed Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Schindler Disease | Knobloch Syndrome | Exfoliative Dermatitis | Hepatic Veno-occlusive Disease | HIBCH Deficiency | Measles | Acquired Partial Lipodystrophy | Behcet's Disease | Mosaic Variegated Aneuploidy Syndrome 2 | Giant Axonal Neuropathy | Chronic Beryllium Disease | Vascular Calcification | Retinal Vasculitis | Gitelman Syndrome | Spinocerebellar Ataxia Type 17 | Hyperuricemia | Hypodontia | Cutaneous T-cell Lymphoma | Hyperekplexia | Dent Disease | Panuveitis | Microphthalmia | Gardner Syndrome | Williams Syndrome | Nemaline Myopathy | GATA2 Deficiency | Antley-Bixler Syndrome | Spinocerebellar Ataxia Type 5 | Optic Neuropathy, Anterior Ischemic | Mucolipidosis Type IV | Charcot-Marie-Tooth Disease Axonal Type 2N | Pericarditis | Multicystic Renal Dysplasia | Acute Coronary Syndrome | Thanatophoric Dysplasia Type 1 | Crimean-Congo Hemorrhagic Fever | Lymphomatoid Granulomatosis | Ophthalmoplegia | Epidermolysis Bullosa Simplex, Localized | Immunoproliferative Disorders | C3 Glomerulonephritis | Primary Familial Brain Calcification | Leukoplakia | Temtamy Preaxial Brachydactyly Syndrome | Carcinoma, Small Cell | Hemimegalencephaly | Sensory Neuropathy | Hyperinsulinemia | Hoyeraal-Hreidarsson Syndrome | Chorioretinitis | REM Sleep Behavior Disorder | Corneal Ulcer | Chronic Neutrophilic Leukemia | Duane Retraction Syndrome | Diverticulitis | Wolfram Syndrome | Corneal Dystrophies, Hereditary | Muir-Torre Syndrome | Anemia | Lactose Intolerance | Autosomal Recessive Congenital Ichthyosis | Hypertriglyceridemia | Corneal Dystrophy | Spinal Muscular Atrophy | Cholecystitis | Ulcerative Colitis | Cockayne Syndrome | Apraxia | Oligodendroglioma | Stuve-Wiedemann Syndrome | Waardenburg Syndrome | Osteogenesis Imperfecta Type V | IMAGe Syndrome | Antisynthetase Syndrome | Cervical Dystonia | Myelomeningocele | Angioedema, Hereditary | Exocrine Pancreatic Insufficiency | Porphyria, Acute Intermittent | Long QT Syndrome Type 1 | Triple A Syndrome | Cri-du-chat Syndrome | Shock, Cardiogenic | Esophageal Carcinoma | Charcot-Marie-Tooth Disease Type 4B1 | Auriculocondylar Syndrome | Celiac Disease | Cerebellar Ataxia, Cayman Type | Panic Disorder | Albinism