Disease

Lamellar Ichthyosis

About the Disease
Autosomal Recessive Congenital Ichthyosis, also known as lamellar ichthyosis, is related to ichthyosis, congenital, autosomal recessive 1 and ichthyosis, congenital, autosomal recessive 2. An important gene associated with Autosomal Recessive Congenital Ichthyosis is ALOX12B (Arachidonate 12-Lipoxygenase, 12R Type), and among its related pathways/superpathways are Keratinization and Prostaglandin 2 biosynthesis and metabolism FM. The drugs Bezafibrate and Ustekinumab have been mentioned in the context of this disorder. Affiliated tissues include skin, eye and subthalamic nucleus, and related phenotypes are ichthyosis and abnormality of the nail

Common Targets
SPINK5 | CYP17A1 | TGM1 | ALOXE3 | SDR9C7 | CYP4F22 | ALOX12B | CERS3 | NIPAL4 | RARG | SLC26A4 | PNPLA1

疾病靶点研报
Lamellar Ichthyosis

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

Other Diseases

Transcobalamin Deficiency | Maple Syrup Urine Disease | Rhizomelic Chondrodysplasia Punctata | Asperger Syndrome | Ghosal Syndrome | Extramammary Paget's Disease | Episodic Ataxia | Bare Lymphocyte Syndrome | Cerebrovascular Disorders | Crimean-Congo Hemorrhagic Fever | Renal Tubular Dysgenesis | Rhabdomyosarcoma, Embryonal | Congenital Dyserythropoietic Anemia Type 1 | Spinocerebellar Ataxia Type 12 | Wagner Disease | HIBCH Deficiency | Androgenic Alopecia | Alkaptonuria | Neurofibrosarcoma | Papillon-Lefevre Syndrome | Cherubism | Congenital Adrenal Hyperplasia 1 | Pfeiffer Syndrome | Glycogen Storage Disease Type 9 | Histoplasmosis | Uremia | Meleda Disease | Ectrodactyly | Vulvovaginitis | Dermatomyositis | Sclerocornea | Split Hand-foot Malformation | X-linked Charcot-Marie-Tooth Disease | Tietze Syndrome | Osteoarthritis | Exfoliative Dermatitis | Autosomal Recessive Bestrophinopathy | Early Infantile Epileptic Encephalopathy 1 | Atrial Septal Defect | Hypertension, Renal | Pontocerebellar Hypoplasia Type 7 | Schizotypal Personality Disorder | Viral Meningitis | Xeroderma Pigmentosum Variant Type | Stuttering | Hypobetalipoproteinemias | Muir-Torre Syndrome | Meconium Ileus | Arteriovenous Malformations | Focal Segmental Glomerulosclerosis | Infertility, Male | Hypodontia | Scapuloperoneal Spinal Muscular Atrophy | Fuchs Dystrophy | Waardenburg Syndrome Type 2E | Leukemia | Jalili Syndrome | Ventricular Septal Defect | Oculocutaneous Albinism Type 2 | Binge Eating Disorder | Best Macular Dystrophy | Kallmann Syndrome | Spondylo-ocular Syndrome | Pain | Congenital Fiber-type Disproportion Myopathy | T-cell Lymphoma, Subcutaneous Panniculitis-like | Hemorrhagic Disorders | Glycogen Storage Disease Type 0, Muscle | Overactive Bladder | Major Depression | Lipid Storage Myopathy | Diabetes Gestational | Menetrier Disease | Bainbridge-Ropers Syndrome | Odonto-onycho-dermal Dysplasia | Hyperlipidemia, Familial Combined | Renpenning Syndrome | Shock, Cardiogenic | Hyperostosis | Large Granular Lymphocytic Leukemia | Liddle Syndrome | Cancer, Lung | TARP Syndrome | Cancer, Brain | Myofibrillar Myopathy | Spinocerebellar Ataxia Type 6 | Hepatitis B, Chronic | Tricho-hepato-enteric Syndrome | Cocaine-Related Disorders | Histiocytic Sarcoma | Diabetes Type 1 | Migraine | Purpura, Thrombotic Thrombocytopenic | Veno-occlusive Disease | Gestational Trophoblastic Disease | Oguchi Disease-2 | Galactosemia | Myosin Storage Myopathy | Combined Pituitary Hormone Deficiency | Influenza | Granuloma Annulare | Hemochromatosis Type 1 | DRESS Syndrome | Optic Nerve Diseases | Syncope | Myhre Syndrome | Woodhouse-Sakati Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Ollier Disease | Hidradenitis | Schnitzler Syndrome | Trichomegaly | Takotsubo Cardiomyopathy | Lassa Fever | Celiac Disease | Rubinstein-Taybi Syndrome | Salla Disease | Borjeson-Forssman-Lehmann Syndrome | Emery-Dreifuss Muscular Dystrophy | Pompe Disease | Yellow Fever | Mabry Syndrome | Amenorrhea | Colitis | Rickets | Cholangitis | Dupuytren Disease | Kleine-Levin Syndrome | Myelitis, Transverse | Mitochondrial Cytopathy | Hepatic Adenomatosis | Plasma Cell Dyscrasia | Hemorrhage | Cerebellar Ataxia, Cayman Type | Pseudohypoparathyroidism Type 1C | Parkinson's Disease | Tremor | Hypogonadism | Subacute Sclerosing Panencephalitis | Auriculocondylar Syndrome | Papilledema | Charcot-Marie-Tooth Disease Type 2D | Chronic Periodontitis | Urea Cycle Disorder | Pyloric Stenosis, Infantile Hypertrophic | Glomerulonephritis | Idiopathic Pulmonary Fibrosis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Mosaic Variegated Aneuploidy Syndrome 2 | Epidermolysis Bullosa | Vitreoretinal Degeneration, Snowflake Type | Myoclonic Epilepsy With Ragged Red Fibers | Congenital Tufting Enteropathy | Congenital Bile Acid Synthesis Defect | Imerslund-Grasbeck Syndrome | Eating Disorder | Hypercholesterolemia | Behavioral Variant Of Frontotemporal Dementia | Pyruvate Dehydrogenase Deficiency | GATA2 Deficiency | Hyperlipidemia Type V | Paroxysmal Nocturnal Hemoglobinuria | Lennox-Gastaut Syndrome | Anxiety Disorders | Paraplegia | Potocki-Shaffer Syndrome | Hyperbilirubinemia, Neonatal | Chronic Idiopathic Myelofibrosis | Tendinopathy | Hoyeraal-Hreidarsson Syndrome | Familial Cerebral Amyloid Angiopathy | Multiple Epiphyseal Dysplasia | Diabetes Insipidus, Neurogenic | Pseudohypoparathyroidism Type 1A | Patent Foramen Ovale | Wolfram Syndrome 2 | Renal Tubular Acidosis | Retinal Detachment | Cholestasis | Cardiomyopathy, Hypertrophic | Glycogen Storage Disease Type 6 | Hyperuricemia | Cryopyrin-associated Periodic Syndromes | Alopecia Areata | VACTERL Association | Pyruvate Carboxylase Deficiency Disease | Huntington's Disease-like 2 | Dent Disease | Nevus | Hypervalinemia | Niemann-Pick Disease, Type B | Gnathodiaphyseal Dysplasia | Ameloblastoma | Ameloblastic Carcinoma | Blood Protein Disorders | Spinocerebellar Ataxia Type 3 | Hypercholesterolemia, Familial | Keratoconjunctivitis | Tracheal Disorders | Pontocerebellar Hypoplasia | Amebiasis | Cirrhosis | Spinocerebellar Ataxia Type 7 | DOCK8 Immunodeficiency Syndrome | Parkinson Disease 6, Autosomal Recessive Early-onset | Hepatitis A | Hypoparathyroidism | MELAS Syndrome | Persistent Hyperplastic Primary Vitreous | Toxic Epidermal Necrolysis | Macrophage Activation Syndrome | Chromosome 5q Deletion Syndrome | Aicardi-Goutieres Syndrome | Joubert Syndrome | Adenomatoid Tumor | Intracranial Hypertension | Cerebellofaciodental Syndrome | Stroke, Ischemic | Necrobiosis Lipoidica | Frank-ter Haar Syndrome | Fibromyalgia | Primary Hyperoxaluria Type 1 | Mitochondrial Disease | Inflammatory Linear Verrucous Epidermal Nevus | Hartsfield Syndrome | Coffin-Siris Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Osteoporosis, Postmenopausal | Spinal Muscular Atrophy Type 2 | Pyruvate Decarboxylase Deficiency | Agammaglobulinemia | Canavan Disease | Long QT Syndrome Type 1 | Neurofibroma, Plexiform | Glaucoma, Congenital | Leukoplakia | Chondrosarcoma | Nephrocalcinosis | Pleurisy | Asthma, Exercise-induced | Growth Hormone Excess | Hypereosinophilic Syndrome | McLeod Syndrome | Tuberculous Meningitis | Heterotaxy | Inflammatory Joint Disease | Pseudohypoaldosteronism | Allan-Herndon-Dudley Syndrome | Pterygium | Intestinal Obstruction | Robinow Syndrome | Neurofibroma | Distal Spinal Muscular Atrophy | Lymphedema-distichiasis Syndrome | Neuroblastoma | Hereditary Pyropoikilocytosis | Polycythemia | Spinal Muscular Atrophy Type 3 | Infectious Diarrhea | Klinefelter Syndrome | Christianson Syndrome | Wieacker-Wolff Syndrome | Pulmonary Capillary Hemangiomatosis | Asthma, Nocturnal | Early Infantile Epileptic Encephalopathy 4 | Ectodermal Dysplasia | Creatine Deficiency Syndrome Due To AGAT Deficiency | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Polycystic Kidney, Autosomal Recessive | Silver-Russell Syndrome | Benign Hereditary Chorea | Pseudohermaphroditism | Carcinoid Syndrome | Retinoblastoma | Lattice Corneal Dystrophy | Von Willebrand Disease | Lipid Storage Diseases | Inflammatory Myopathy | Hypolipoproteinemia | Learning Disability | Postpoliomyelitis Syndrome | Pneumonia, Bacterial | Autosomal Recessive Spastic Paraplegia Type 54 | Hyperekplexia | Bruck Syndrome | Spitzoid Melanoma | Phenylketonuria | Aromatic L-amino Acid Decarboxylase Deficiency | Bernard-Soulier Syndrome | Dysequilibrium Syndrome | Stiff-man Syndrome | Primary Biliary Cholangitis | H Syndrome | Birt-Hogg-Dube Syndrome | Multiple Sclerosis, Secondary Progressive | Spondylocarpotarsal Synostosis Syndrome | Spinocerebellar Ataxia Type 40 | Rheumatoid Arthritis | Hypertrophy | Cataplexy | Shprintzen-Goldberg Syndrome | Neurodegeneration With Brain Iron Accumulation | Stickler Syndrome | Dwarfism | Chronic Beryllium Disease | Cancer, Kidney | Porokeratosis | Epidermodysplasia Verruciformis | Spinocerebellar Ataxia Type 13 | Thalassemia, Beta | Beta-Propeller Protein-associated Neurodegeneration | Long QT Syndrome Type 3 | Familial Hypobetalipoproteinemia | Cockayne Syndrome | Epidermolysis Bullosa Simplex, Generalized | Impulse Control Disorder | Cryptorchidism | Progressive Familial Intrahepatic Cholestasis Type 2 | Waardenburg Syndrome Type 2 | Paronychia | Riboflavin Transporter Deficiency Neuronopathy | Barakat Syndrome | Uveitis | Glutaric Aciduria Type 3 | Fatty Aldehyde Dehydrogenase Deficiency | Pycnodysostosis | Perivascular Epithelioid Cell Tumor | Cervical Dystonia | Myocarditis | Bulimia Nervosa | Charcot-Marie-Tooth Disease Type 4B1 | Thyroid Dyshormonogenesis | Von Hippel-Lindau Disease | DEND Syndrome | Pneumoconiosis | Epithelial-myoepithelial Carcinoma | Bicuspid Aortic Valve | Methylmalonic Aciduria And Homocystinuria, CblC Type | Intestinal Pseudo-obstruction | Budd-Chiari Syndrome | Demyelinating Diseases | Carcinoma, Signet Ring Cell | Trachoma | Olmsted Syndrome | GLUT1 Deficiency Syndrome | Congestive Heart Failure | Sarcoma | Choriocarcinoma | Usher Syndrome Type IIC | Congenital Afibrinogenemia | Congenital Aniridia | Pituitary Disorders | Multicystic Renal Dysplasia | Reye Syndrome | Motion Sickness | Multiple Sclerosis | Pure Autonomic Failure | Tylosis With Esophageal Cancer | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Purpura | Neuroectodermal Tumors, Primitive | Sweet Syndrome | Hereditary Sensory And Autonomic Neuropathy | Early Infantile Epileptic Encephalopathy 13 | Carpal Tunnel Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Specific Granule Deficiency | L-2-Hydroxyglutaric Aciduria | Neurofibromatosis | AIDS | Huntington's Disease | Dominant Optic Atrophy | Apert Syndrome | Adult Polyglucosan Body Disease | Myositis | Alopecia | Keratosis | Glomerulonephritis, Membranous | Cutaneous Lupus Erythematosus | Common Cold | Hypogammaglobulinemia | Osteogenesis Imperfecta Type V | Cutaneous Angiosarcoma | Diamond-Blackfan Anemia | Heroin Dependence | Erythema Multiforme | Encephalocele | Hepatic Steatosis | Leri-Weill Dyschondrosteosis | Acral Lentiginous Melanoma | Acute Myeloid Leukemia | Diabetes Insipidus, Nephrogenic | Communication Disorders | Cardiofaciocutaneous Syndrome | Hypothalamic Obesity | Lipoma | Enlarged Vestibular Aqueduct | Blepharoconjunctivitis | Acromesomelic Dysplasia