Disease

Annular Epidermolytic Ichthyosis

About the Disease
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis, also known as annular epidermolytic ichthyosis, is related to ichthyosis and autosomal dominant epidermolytic ichthyosis. An important gene associated with Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis is KRT10 (Keratin 10), and among its related pathways/superpathways is Keratinization. Affiliated tissues include skin, and related phenotypes are erythema and palmoplantar hyperkeratosis

Common Targets
KRT1 | KRT10

疾病靶点研报
Annular Epidermolytic Ichthyosis

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

Other Diseases

Autosomal Recessive Spastic Paraplegia Type 35 | Pneumonia, Bacterial | Carcinoma, Squamous Cell | Blue Rubber Bleb Nevus Syndrome | Obesity | Common Variable Immunodeficiency | Kearns-Sayre Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Limb Girdle Muscular Dystrophy | Osteoporosis-pseudoglioma Syndrome | Cancer, Breast | Potocki-Shaffer Syndrome | Esophageal Carcinoma | Burn-McKeown Syndrome | Meckel-Gruber Syndrome | Periodontitis | Lamellar Ichthyosis | Eclampsia | Chronic Neutrophilic Leukemia | Peeling Skin Syndrome, Acral Type | Tenosynovial Giant Cell Tumor | Alpha-1 Antitrypsin Deficiency | Exocrine Pancreatic Insufficiency | Bicuspid Aortic Valve | Urolithiasis | WAGR Syndrome | Personality Disorders | Corneal Edema | Cutis Laxa | Influenza | Otopalatodigital Syndrome Type 2 | DiGeorge Syndrome | Protein C Deficiency | Encephalitis, Tick-borne | Coma | Basan Syndrome | Epiphyseal Chondrodysplasia, Miura Type | Chronic Beryllium Disease | Cryptorchidism | Rothmund-Thomson Syndrome | Marinesco-Sjogren Syndrome | Mitochondrial Cytopathy | Saul-Wilson Syndrome | Persistent Fetal Circulation | Pseudoachondroplasia | Torticollis | Pelvic Inflammatory Disease | Down Syndrome | Hereditary Elliptocytosis | Hypercholesterolemia | Pineoblastoma | Neurocysticercosis | Tularemia | Familial Retinal Arterial Macroaneurysm | Ichthyosis, X-linked | Blau Syndrome | Hereditary Hemorrhagic Telangiectasia | Nicotine Dependence | Hyperparathyroidism, Secondary | Brachial Plexus Neuropathy | VEXAS Syndrome | HELLP Syndrome | Arthritis, Reactive | Blepharitis | Hyperuricemic Nephropathy, Familial Juvenile | Aspergillosis | Heroin Dependence | Postpoliomyelitis Syndrome | Myofibrillar Myopathy | Teratozoospermia | Vitamin K Deficiency | Alkaptonuria | Triphalangeal Thumb-polysyndactyly Syndrome | Diabetic Macular Edema | Metanephric Adenoma | Meleda Disease | Pneumonia, Mycoplasma | Depression | Spinocerebellar Ataxia Type 28 | Maple Syrup Urine Disease | Renal Tubular Dysgenesis | Sweet Syndrome | Chorioretinitis | Cantu Syndrome | Kabuki Syndrome 2 | Skin Carcinoma | Epithelial-myoepithelial Carcinoma | Neurodermatitis | Crouzon Syndrome With Acanthosis Nigricans | Noonan Syndrome | Mabry Syndrome | Kaposi Sarcoma | Cutaneous T-cell Lymphoma | Keratoacanthoma | Lateral Meningocele Syndrome | Primary Cutaneous Amyloidosis | Phenylketonuria II | Avellino Corneal Dystrophy | Alagille Syndrome | Myoclonic Atonic Epilepsy | Tylosis With Esophageal Cancer | Castleman Disease | Leukocyte Adhesion Deficiency Type 1 | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Intermittent Explosive Disorder | Hemophagocytic Lymphohistiocytosis | Charcot-Marie-Tooth Disease, Type 2C | Usher Syndrome Type II | Hypohidrotic Ectodermal Dysplasia | Osteogenesis Imperfecta Type VI | Specific Granule Deficiency | Non-small Cell Lung Cancer | Enlarged Vestibular Aqueduct | Stiff-man Syndrome | Leukoencephalopathy, Progressive Multifocal | Congestive Heart Failure | Vitreoretinopathy, Proliferative | Pupil Disorders | Adult Polyglucosan Body Disease | Takotsubo Cardiomyopathy | Hereditary Hemorrhagic Telangiectasia Type 2 | Obsessive-compulsive Disorder | Sensory Neuropathy | Argininosuccinic Aciduria | Microcephalic Primordial Dwarfism | Zimmermann-Laband Syndrome | Adrenomyeloneuropathy | Cold Agglutinin Disease | Cerebellar Ataxia, Cayman Type | Aldosterone Deficiency | Neovascular Glaucoma | Spinocerebellar Ataxia Type 20 | Myelitis, Transverse | Niemann-Pick Disease, Type B | Apparent Mineralocorticoid Excess Syndrome | Pontocerebellar Hypoplasia Type 2 | Dysthymia | Familial Exudative Vitreoretinopathy | Paroxysmal Nocturnal Hemoglobinuria | Alopecia Areata | Retinal Detachment | Wolfram Syndrome | Salla Disease | ICF Syndrome | Gnathodiaphyseal Dysplasia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Graves Disease | Acute Chest Syndrome | Temporal Lobe Epilepsy | Hemochromatosis Type 1 | Pulmonary Sclerosing Hemangioma | Spinocerebellar Ataxia Type 16 | Takenouchi-Kosaki Syndrome | Meesmann Corneal Dystrophy | Aplasia Cutis Congenita | Cavitary Optic Disc Anomalies | Proctitis | Angiomyolipoma | Echinococcosis | Chloridorrhea, Congenital | Retinitis | Tyrosinemia Type 1 | Neutropenia | Li-Fraumeni Syndrome | Schwartz-Jampel-Aberfeld Syndrome | Glutaric Aciduria Type 2 | Dystrophy, Cone-rod | Poretti-Boltshauser Syndrome | Gliosarcoma | Iron Deficiency Anemia | Pseudohypoaldosteronism | Disseminated Superficial Actinic Porokeratosis | Kabuki Syndrome | Neuronal Ceroid Lipofuscinosis | Bietti Crystalline Dystrophy | Menkes Disease | Combined Pituitary Hormone Deficiency | Anorchia | Alcoholism | Waardenburg Syndrome Type 2 | Mucolipidosis | Lung Diseases | Bronchiolitis | Dyslexia | Vitreoretinal Degeneration, Snowflake Type | LRBA Deficiency | Stevens-Johnson Syndrome | Neurofibromatosis Type 2 | Chromosome 17q21.31 Deletion Syndrome | Cannabis Abuse | Malaria | Feingold Syndrome | Steel Syndrome | Dominant Optic Atrophy | Cri-du-chat Syndrome | Osteoporosis, Postmenopausal | Peyronie's Disease | Hypercalciuria | Tetraplegia | Encephalopathy | NDH Syndrome | LEOPARD Syndrome | Tremor | Leber Congenital Amaurosis | Epithelioid Hemangioma | Panuveitis | Learning Disability | Chordoid Glioma | Split Hand-foot Malformation | Cardiomyopathy, Dilated, 1L | Juvenile Polyposis | Lymphoma, AIDS-related | Tangier Disease | Charcot-Marie-Tooth Disease Type 4B1 | Gigantism | Hypohidrotic Ectodermal Dysplasia, X-linked | Malnutrition | Atrioventricular Septal Defect | Thrombocythemia, Essential | Familial Digital Arthropathy-brachydactyly | Optic Nerve Diseases | Cheilitis | Hemorrhage | Congenital Dyserythropoietic Anemia Type 1 | Long QT Syndrome Type 1 | Pneumoconiosis | Charcot-Marie-Tooth Disease, Type 2A | Chronic Lymphocytic Leukemia | Pseudohypoparathyroidism Type 1C | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Hypotonia-cystinuria Syndrome | Dysmorphophobia | Colitis, Lymphocytic | Charcot-Marie-Tooth Disease Axonal Type 2N | Cohen Syndrome | Porokeratosis | Dermatomyositis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Tonsillitis | Vestibular Disease | Apert Syndrome | Hepatitis C, Chronic | Guanidinoacetate Methyltransferase Deficiency | Silver-Russell Syndrome | Charcot-Marie-Tooth Disease Type 3 | Carney-Stratakis Syndrome | Ehlers-Danlos Syndrome | L-2-Hydroxyglutaric Aciduria | Carcinoma, Transitional Cell | Pre-eclampsia | Oligoasthenoteratozoospermia | Glomerulonephritis | Waardenburg Syndrome | Basal Ganglia Disease | Focal Cortical Dysplasia Type 2 | Transcobalamin Deficiency | Marshall-Smith Syndrome | Usher Syndrome Type III | Yellow Fever | Gangliosidosis, GM1 | Cholestasis, Intrahepatic | Preaxial Polydactyly | Thrombophlebitis | Epidermolysis Bullosa | Meier-Gorlin Syndrome | Congenital Adrenal Hyperplasia 1 | Jawad Syndrome | Hypospadias | Focal Dermal Hypoplasia | Mitochondrial DNA Depletion Syndrome | Progressive Myoclonic Epilepsy | Spinocerebellar Ataxia Type 1 | Plasma Cell Leukemia | Autosomal Recessive Spastic Paraplegia Type 75 | Polycystic Ovary Syndrome | AIDS Dementia Complex | Malignant Peripheral Nerve Sheath Tumor | Ependymoma | CHARGE Syndrome | Fibrodysplasia Ossificans Progressiva | Aarskog-Scott Syndrome | Chronic Granulomatous Disease | Acrodermatitis | Pain | Pneumococcal Meningitis | Trichorhinophalangeal Syndrome | Pituitary Dwarfism | Encephalopathy, Glycine | Mitochondrial Encephalomyopathy | Inflammatory Myofibroblastic Tumor | Retinal Dystrophy | Multiple Sclerosis, Chronic Progressive | Trigonocephaly | Dyggve-Melchior-Clausen Disease | Parkinson's Disease | Hypertensive Retinopathy | Anti-NMDA Receptor Encephalitis | Acanthosis Nigricans | Congenital Sodium Diarrhea | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Guttate Psoriasis | Oculocutaneous Albinism Type 1 | Renal Tubular Acidosis | Primary Familial Brain Calcification | Porencephaly | Familial Dysautonomia | Craniometaphyseal Dysplasia | Vasculitis | Prurigo Nodularis | Neuromuscular Disorders | Distal Myopathy 2 | Peroxisomal Disorder | Anxiety Disorders | Congenital Poikiloderma | Lichen Planus | Ligneous Conjunctivitis | Sick Sinus Syndrome | Charcot-Marie-Tooth Disease, Type 2 | Focal Facial Dermal Dysplasia | B-cell Chronic Lymphocytic Leukemia | Spinocerebellar Ataxia Type 15 | Stickler Syndrome | Papulopustular Rosacea | Polyneuropathy | Congenital Hereditary Endothelial Dystrophy Type II | Progressive Familial Intrahepatic Cholestasis Type 3 | Spondyloepiphyseal Dysplasia Tarda, X-linked | Fuchs Heterochromic Iridocyclitis | Pyruvate Decarboxylase Deficiency | T-cell Chronic Lymphocytic Leukemia | Chronic Thromboembolic Pulmonary Hypertension | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Multiple Sclerosis, Primary Progressive | Spinocerebellar Ataxia Type 21 | Iron Overload | Leri Pleonosteosis | Epidermolysis Bullosa Acquisita | Intracranial Hypertension | Osteogenesis Imperfecta Type II | Myeloid Leukemia | Meningitis | Hydrocephalus, Normal Pressure | Leiomyoma | Chondrodysplasia Punctata 2, X-linked Dominant | Pituitary Stalk Interruption Syndrome | Tatton-Brown-Rahman Syndrome | Melanoma, Uveal | Lymphangiomatosis | Relapsing Polychondritis | Dysfibrinogenemia | Thanatophoric Dysplasia | Motion Sickness | Spinocerebellar Ataxia Type 7 | Rhinitis | Vici Syndrome | Albinism | Isovaleric Acidemia | Pancytopenia | Hyperkalemic Periodic Paralysis | Sotos Syndrome | Non-Langerhans Cell Histiocytosis | Erythema Multiforme | Rickets | Lipid Storage Diseases | Giant Axonal Neuropathy | Communication Disorders | Choriocarcinoma | Juvenile Myoclonic Epilepsy | Heart Failure | HIBCH Deficiency | Compartment Syndrome | Asphyxia Neonatorum | Cutaneous Lupus Erythematosus | Corneal Ulcer | Fuchs Dystrophy | Osteosclerosis | Esotropia | Pulmonary Alveolar Proteinosis | Tuberculosis | Progressive Familial Intrahepatic Cholestasis | Parkinsonism | Schwannoma | Superficial Spreading Melanoma | Hyperglycemia | Pfeiffer Syndrome | Cataplexy | Erdheim-Chester Disease | Kawasaki Disease | Leishmaniasis, Visceral | Hyperprolactinemia | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Sclerosteosis 2 | Binge Eating Disorder | Major Depression | Thyroiditis, Autoimmune | Pendred Syndrome | Neuromyelitis Optica | Cryptococcal Meningitis | Basal Cell Nevus Syndrome