Subcortical Band Heterotopia

About the Disease
Band Heterotopia, also known as subcortical band heterotopia, is related to lissencephaly 1 and lissencephaly, x-linked, 1. An important gene associated with Band Heterotopia is EML1 (EMAP Like 1), and among its related pathways/superpathways are Signal Transduction and "Cell Cycle, Mitotic". Affiliated tissues include cortex, brain and fetal brain, and related phenotypes are macrocephaly and spasticity

Common Targets
DCX | EML1 | PAFAH1B1

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

Other Diseases

Pseudoexfoliation Syndrome | Peeling Skin Syndrome, Acral Type | Oral Lichen Planus | Dyggve-Melchior-Clausen Disease | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Varicocele | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Corneal Ulcer | Nance-Horan Syndrome | Neurofibrosarcoma | Thyroid Dysgenesis | Saethre-Chotzen Syndrome | Anti-glomerular Basement Membrane Disease | Analgesia | Hepatitis, Autoimmune | Tic Disorder | Alpha-thalassemia Myelodysplasia Syndrome | Nephropathy | Jalili Syndrome | Methemoglobinemia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Myositis, Focal | Primary Hyperoxaluria | Obsessive-compulsive Disorder | Connective Tissue Disorders | Trimethylaminuria | Liver Failure | Carcinoid Syndrome | Sarcoma, Alveolar Soft Part | Glycogen Storage Disease Type 0 | Kohlschutter-Tonz Syndrome | Apraxia | 3-hydroxy-3-methylglutaric Aciduria | Alazami Syndrome | Hypobetalipoproteinemias | Adenocarcinoma | Hepatitis C, Chronic | Cysticercosis | Lissencephaly 2 | Chudley-McCullough Syndrome | Spinocerebellar Ataxia Type 42 | Persistent Mullerian Duct Syndrome | Heart Septal Defects | Episodic Ataxia Type 1 | Systemic Lupus Erythematosus | Chondrodysplasia Punctata 1, X-linked Recessive | Graves Disease | Leukocyte Adhesion Deficiency | Sialidosis | Necrobiosis Lipoidica | Hyperlipidemia | Schwannoma | Parkinson's Disease | Aspergillosis | Ectodermal Dysplasia | Hemimegalencephaly | Rett Syndrome | Esophagitis, Eosinophilic | Torticollis | Diabetic Nephropathy | Infantile Nephropathic Cystinosis | Carcinoma, Signet Ring Cell | Enlarged Vestibular Aqueduct | Diarrhea | Wolman Disease | Arthritis, Psoriatic | Beta-Propeller Protein-associated Neurodegeneration | Angioedema, Hereditary | Vulvovaginitis | Disseminated Superficial Actinic Porokeratosis | Fetal Alcohol Syndrome | Myelodysplasia | Infantile Spasm | Sotos Syndrome | Chronic Granulomatous Disease, X-linked | Neurodevelopmental Disorders | Alveolar Capillary Dysplasia | Acute Coronary Syndrome | Tumoral Calcinosis | Alopecia Areata | Pneumonia, Viral | Sclerocornea | Bone Marrow Necrosis | Olmsted Syndrome | Feingold Syndrome | Toxoplasmosis | Hypopituitarism | Vitelliform Macular Dystrophy | Aplasia Cutis Congenita | Mitochondrial Cytopathy | Kabuki Syndrome | Peutz-Jeghers Syndrome | Hypotrichosis | Amblyopia | Colorectal Adenoma | Whipple's Disease | Hemochromatosis Type 2 | Osteomyelitis | Progressive Familial Intrahepatic Cholestasis | Dominant Optic Atrophy | GNE Myopathy | Hemangioblastoma | Premature Ejaculation | Bruck Syndrome | Chromosome 8q21.11 Deletion Syndrome | Paternal Uniparental Disomy Of Chromosome 14 | Kallmann Syndrome | Cushing Syndrome | Acrodermatitis | Niemann-Pick Disease, Type A | T-cell Prolymphocytic Leukemia | Mabry Syndrome | Anuria | Evans Syndrome | T-cell Chronic Lymphocytic Leukemia | Pseudohypoparathyroidism Type 2 | Corneal Dystrophy And Perceptive Deafness | PASLI Disease | Carbamoyl Phosphate Synthetase I Deficiency | Vitreoretinopathy, Proliferative | Acromicric Dysplasia | Toxic Epidermal Necrolysis | Gitelman Syndrome | Tendinopathy | Desbuquois Syndrome | Carcinoma, Merkel Cell | Crisponi Syndrome | Epidermolytic Ichthyosis, Annular | Seborrheic Dermatitis | Thyroiditis | Hypersensitivity Pneumonitis | Takotsubo Cardiomyopathy | Clouston Hidrotic Ectodermal Dysplasia | Lennox-Gastaut Syndrome | Glycogen Storage Disease Type 1a | Cornelia De Lange Syndrome | Primary Cutaneous Amyloidosis | Atrial Septal Defect | Chronic Myelomonocytic Leukemia | Achondrogenesis | Bicuspid Aortic Valve | Hypoglycemia | Histoplasmosis | Spondylolisthesis | Chiari Malformation Type I | Carpal Tunnel Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Rheumatoid Arthritis | HIBCH Deficiency | Synpolydactyly | Papilloma | Peripheral T-cell Lymphoma | Osteogenesis Imperfecta | Scleroderma | Malaria | Cystinuria | Polycystic Kidney, Autosomal Recessive | Gilbert Syndrome | N-acetylglutamate Synthase Deficiency | Heavy Chain Disease | Gastrointestinal Disorders | Celiac Disease | Multicentric Carpotarsal Osteolysis Syndrome | Fuchs Heterochromic Iridocyclitis | Sclerosteosis 2 | Papillon-Lefevre Syndrome | Brachydactyly | Cholangitis | Idiopathic Pulmonary Fibrosis | Pre-eclampsia | Spinocerebellar Ataxia Type 40 | Anodontia | Macrodactyly | Pyruvate Dehydrogenase Deficiency | Glycogen Storage Disease Type 4 | Splenomegaly | Glucagonoma | Herpes Simplex Dermatitis | Charcot-Marie-Tooth Disease, Type 2 | Larsen Syndrome | Lattice Corneal Dystrophy | Distal Spinal Muscular Atrophy | Autoimmune Polyendocrinopathy Syndrome Type I | Combined Deficiency Of Factor V And Factor VIII | Mountain Sickness | Gout | Canavan Disease | Epidermodysplasia Verruciformis | Rubinstein-Taybi Syndrome | Salla Disease | Hyperkeratosis | Leber Hereditary Optic Neuropathy | Epilepsy Of Infancy With Migrating Focal Seizures | Prolymphocytic Leukemia | Dermatomyositis | Dengue Hemorrhagic Fever | Vertigo | Hyperkalemic Periodic Paralysis | Papulopustular Rosacea | Charcot-Marie-Tooth Disease, Type 2C | High Molecular Weight Kininogen Deficiency | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Rash | Juvenile Myoclonic Epilepsy | Duodenal Atresia | Charcot-Marie-Tooth Disease | COACH Syndrome | Hartnup Disease | Lentigo | Hereditary Folate Malabsorption | Smith-Lemli-Opitz Syndrome | Lymphangiomatosis | NGLY1 Deficiency | Osteogenesis Imperfecta Type IV | Isovaleric Acidemia | Liver Diseases | Scoliosis | GLUT1 Deficiency Syndrome | Presbycusis | Cerebrotendinous Xanthomatosis | Gigantism | Diabetic Encephalopathy | Autoimmune Hemolytic Anemia | Leukemia | Osteogenesis Imperfecta Type V | Hemangioma | Spinocerebellar Ataxia Type 10 | Echinococcosis | Hyperparathyroidism, Secondary | Enhanced S-cone Syndrome | Adrenal Insufficiency | Fibrillation, Atrial | Cluster Headache | Demyelinating Diseases | Melanocytic Nevus | Hyperlipidemia, Familial Combined | Non-Hodgkin Lymphoma | Schindler Disease | Subcortical Band Heterotopia | Persistent Truncus Arteriosus | Cerebrovascular Disorders | Autoimmune Disease | Corneal Dystrophy | Cystinosis | Spinocerebellar Ataxia Type 8 | Chronic Mucocutaneous Candidiasis | T-cell Lymphoma, Subcutaneous Panniculitis-like | Waardenburg Syndrome Type 4A | Lipid Storage Myopathy | Antiphospholipid Syndrome | Dermatitis Herpetiformis | Hyperhomocysteinemia | Endometrial Hyperplasia | Lipid Storage Diseases | Proopiomelanocortin Deficiency | Charcot-Marie-Tooth Disease, Type 1A | Renal Medullary Carcinoma | Joubert Syndrome | Ligneous Conjunctivitis | Kleine-Levin Syndrome | Migraine | Wolfram Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | Blastoma, Pleuropulmonary | Hamartoma | Aneurysm, Thoracic Aortic | Rift Valley Fever | Juvenile Myelomonocytic Leukemia | Kindler Syndrome | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Primary Ovarian Insufficiency | Sleep Apnea, Central | Keloid | Polymyalgia Rheumatica | Scleroderma, Diffuse | Encephalopathy, Hepatic | Carotid Artery Disease | Sickle Cell Disease | Urethritis | Cohen Syndrome | Giant Cell Glioblastoma | Mesothelioma, Malignant | Pancytopenia | Spinal Muscular Atrophy | Congenital Dyserythropoietic Anemia | Greig Cephalopolysyndactyly Syndrome | Hypogonadism | Progressive Familial Intrahepatic Cholestasis Type 1 | Myositis | Osteoporosis | Episodic Ataxia | Waardenburg Syndrome Type 4 | Carcinoma, Squamous Cell | Malnutrition | X-linked Charcot-Marie-Tooth Disease | Spondylosis | Aphasia | Hyperparathyroidism, Primary | Multiple Myeloma | Infantile Refsum Disease | Sertoli Cell-only Syndrome | Common Variable Immunodeficiency | Frank-ter Haar Syndrome | Gangliosidosis | Hypotrichosis Simplex | Neurofibroma, Plexiform | Schwartz-Jampel-Aberfeld Syndrome | Hypersomnia | Allergic Contact Dermatitis | Ganglioglioma | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Oculocutaneous Albinism | Klippel-Feil Syndrome | Pendred Syndrome | Spondylocostal Dysostosis | Teratozoospermia | Fanconi Syndrome | Macular Corneal Dystrophy Type 1 | Cancer, Colon | Pathological Gambling | Myelofibrosis | Myotonia | Diabetes Mellitus, Transient Neonatal | Fatty Aldehyde Dehydrogenase Deficiency | REM Sleep Behavior Disorder | Hydrops Fetalis | Osteochondroma | Usher Syndrome Type I | Preaxial Polydactyly | Inflammatory Bowel Disease | Polycystic Ovary Syndrome | Oligoastrocytoma | Congenital Hemolytic Anemia | Acne Vulgaris | Chylothorax, Congenital | Craniofrontonasal Syndrome | Acute Chest Syndrome | Gastroenteritis, Eosinophilic | Pycnodysostosis | Hoyeraal-Hreidarsson Syndrome | Tremor | Antley-Bixler Syndrome | Adrenoleukodystrophy, X-linked | Otopalatodigital Syndrome Type 2 | Incontinentia Pigmenti | Seizures-scoliosis-macrocephaly Syndrome | Specific Granule Deficiency | Hemophagocytic Lymphohistiocytosis | Lactose Intolerance | Antenatal Bartter Syndrome Type 1 | Burn-McKeown Syndrome | Ureteropelvic Junction Obstruction | Inborn Errors Of Metabolism | Ehlers-Danlos Syndrome | Hemorrhagic Disorders | Retinitis Pigmentosa 3 | Double Outlet Right Ventricle | Sengers Syndrome | Best Macular Dystrophy | Hereditary Multiple Exostoses | Cryptococcal Meningitis | Stuttering | Aldosterone Deficiency | Insulin Resistance | Meier-Gorlin Syndrome | Spitzoid Melanoma | Stargardt Disease | Ataxia-ocular Apraxia 2 | Congestive Heart Failure | Early Infantile Epileptic Encephalopathy 28 | Cranial Nerve Disease | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Anosmia, Congenital | Primary Pigmented Nodular Adrenocortical Disease | Osteoporosis, Postmenopausal | Anorchia | Arteriosclerosis | Insulinoma | Distal Myopathy 2 | Autism | Smith-Kingsmore Syndrome | Rothmund-Thomson Syndrome | Paraganglioma | Microphthalmia | Glycogen Storage Disease | Congenital Dysfibrinogenemia | Dyslexia | Apert Syndrome | Melanoma, Uveal | Hodgkin Lymphoma | Cutaneous T-cell Lymphoma | Meleda Disease | Bulimia Nervosa | Spinocerebellar Ataxia Type 14 | Multiple Epiphyseal Dysplasia | Encephalopathy, Glycine | Iron Overload | Congenital Myasthenic Syndrome | Schistosomiasis