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

Diabetes Insipidus | Malignant Peripheral Nerve Sheath Tumor | Emery-Dreifuss Muscular Dystrophy | Spinocerebellar Ataxia Type 10 | Cutis Laxa | Pineoblastoma | Charcot-Marie-Tooth Disease, Type 2C | Guillain-Barre Syndrome | Cohen Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Congenital Stationary Night Blindness | Mitochondrial DNA Depletion Syndrome 13 | Hereditary Hemorrhagic Telangiectasia | Eiken Syndrome | Niemann-Pick Disease, Type B | Oral Lichen Planus | Tyrosinemia Type 1 | Adenosine Deaminase 2 Deficiency | Autoimmune Autonomic Ganglionopathy | Progressive External Ophthalmoplegia | Johanson-Blizzard Syndrome | Glycogen Storage Disease Type 1b | Hemorrhoids | Primary Torsion Dystonia | Metanephric Adenoma | Meningitis | Central Retinal Artery Occlusion | Carcinoma, Merkel Cell | Niemann-Pick Disease, Type A | Glycogen Storage Disease Type 6 | Myasthenia Gravis | Thromboembolism | Diffuse Palmoplantar Keratoderma | Hyperbilirubinemia, Neonatal | Multiple System Atrophy | Achondrogenesis | Amebiasis | Prurigo Nodularis | Steel Syndrome | Meningioma, Benign | Moyamoya Disease | Infantile Liver Failure Syndrome 1 | Riboflavin Transporter Deficiency Neuronopathy | Silicosis | Dysthymia | Hamartoma | Niemann-Pick Disease | Encephalitis, Tick-borne | Heterotaxy | Papillorenal Syndrome | Kohlschutter-Tonz Syndrome | Rhabdomyosarcoma, Embryonal | Lymphoproliferative Disease, X-linked | Central Core Disease | HIBCH Deficiency | Glioblastoma Multiforme | Pericarditis | Miyoshi Myopathy | Spinocerebellar Ataxia Type 42 | Fibrillation, Atrial | Narcolepsy | Blau Syndrome | Hypertension | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Woodhouse-Sakati Syndrome | Leprosy | Megalencephaly | Melanoma | Menkes Disease | Noonan Syndrome | Creutzfeldt-Jakob Disease | Dysferlinopathy | Multiple Hamartoma Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Myoclonus | Tietze Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Neuroleptic Malignant Syndrome | Takotsubo Cardiomyopathy | Congenital Tufting Enteropathy | Choroiditis | Geleophysic Dysplasia | Paget's Disease Of The Breast | Anemia | Angioedema, Hereditary | Williams Syndrome | Muscle Wasting | Scapuloperoneal Myopathy, X-linked Dominant | Diffuse Intrinsic Pontine Glioma | Non-Langerhans Cell Histiocytosis | Hypersomnia | Tatton-Brown-Rahman Syndrome | Adult Polyglucosan Body Disease | Necrotizing Autoimmune Myopathy | Ataxia-ocular Apraxia 2 | Renal Failure | Polydactyly | Celiac Disease | Chronic Beryllium Disease | Methemoglobinemia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Cervical Dystonia | Basal Cell Nevus Syndrome | Incontinentia Pigmenti | T-cell Leukemia | Triple A Syndrome | Diabetes Type 1 | Ovarian Hyperstimulation Syndrome | Charcot-Marie-Tooth Disease Type 4D | Cystitis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Basal Ganglia Cerebrovascular Disease | Esophageal Adenocarcinoma | Infantile Spasm | Dysequilibrium Syndrome | Spinocerebellar Ataxia Type 15 | Apert Syndrome | Adenoma, Villous | Generalized Epilepsy And Paroxysmal Dyskinesia | Spinal Muscular Atrophy Type 3 | Hypobetalipoproteinemias | Intestinal Tuberculosis | Familial Cerebral Amyloid Angiopathy | Myoclonic Atonic Epilepsy | AIDS | GM2-gangliosidosis AB Variant | Zellweger Syndrome | Exocrine Pancreatic Insufficiency | Angelman Syndrome | Frontometaphyseal Dysplasia | Polycystic Liver | Adams-Oliver Syndrome | Ocular Hypertension | Ichthyosis Hystrix, Curth-Macklin Type | Dwarfism | Craniometaphyseal Dysplasia | Peeling Skin Syndrome, Acral Type | Tic Disorder | Renal Tubular Dysgenesis | Lymphangioleiomyomatosis | Hepatic Adenomatosis | Nager Acrofacial Dysostosis | Keratitis | Spondylocarpotarsal Synostosis Syndrome | Fuchs Dystrophy | Asphyxia Neonatorum | DRESS Syndrome | Sjogren Syndrome | Urticaria | Congenital Aniridia | McCune-Albright Syndrome | Relapsing Polychondritis | Galactosemia | Pyruvate Decarboxylase Deficiency | Hereditary Hemorrhagic Telangiectasia Type 2 | Carcinoma, Small Cell | Glycogen Storage Disease Type 3 | Spinocerebellar Ataxia Type 23 | Joubert Syndrome 2 | Fatty Aldehyde Dehydrogenase Deficiency | Fundus Albipunctatus | Cardiospondylocarpofacial Syndrome | Thymoma, Malignant | Lipodystrophy | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Oligoasthenoteratozoospermia | Pyelonephritis | Thyroid Hormone Resistance | Reticular Dysgenesis | Corneal Dystrophy And Perceptive Deafness | NDH Syndrome | Rett Syndrome | Genitopatellar Syndrome | Multiple Sclerosis, Primary Progressive | Norrie Disease | Tibial Muscular Dystrophy | Neuromyelitis Optica | Occipital Neuralgia | Cutaneous T-cell Lymphoma | Asthma, Exercise-induced | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Chromosome 8q21.11 Deletion Syndrome | Hyperinsulinemic Hypoglycemia | Familial Hemiplegic Migraine | Keratitis-ichthyosis-deafness Syndrome | Ulcerative Colitis | Pneumonia, Mycoplasma | Cancer, Breast | Fukuyama Congenital Muscular Dystrophy | Coma | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Syndactyly | Osteonecrosis | Early Infantile Epileptic Encephalopathy | Plasmacytoma | Intracerebral Hemorrhage | Oculocutaneous Albinism Type 1 | Jacobsen Syndrome | Metachromatic Leukodystrophy | Shprintzen-Goldberg Syndrome | FG Syndrome | Spinocerebellar Ataxia Type 8 | Antiphospholipid Syndrome | Diabetic Nephropathy | Epiphyseal Chondrodysplasia, Miura Type | ADNP Syndrome | Carney-Stratakis Syndrome | Neuromyotonia | Overactive Bladder | Christianson Syndrome | Pathological Gambling | Keratosis, Seborrheic | Congenital Adrenal Hyperplasia | Retinal Dystrophy | Autonomic Nervous System Disorders | Alopecia | Intestinal Pseudo-obstruction | Diabetic Encephalopathy | Meningeal Melanocytoma | Hereditary Multiple Exostoses | Epidermolysis Bullosa Dystrophica | Retinal Detachment | Lipoma | Thyroid Dysgenesis | Menetrier Disease | Lathosterolosis | Dengue Hemorrhagic Fever | Protein S Deficiency | Endometritis | Stuve-Wiedemann Syndrome | Arthritis, Gouty | Acromicric Dysplasia | Episodic Ataxia Type 2 | Hyperthyroidism | Primary Biliary Cholangitis | Spinocerebellar Ataxia Type 5 | Cockayne Syndrome | Hyperandrogenemia | Autism Spectrum Disorders | Goldenhar Syndrome | DOCK8 Immunodeficiency Syndrome | Creatine Deficiency Syndrome | Schizophrenia | Crigler-Najjar Syndrome | Goiter | Pseudohypoaldosteronism | Aldosterone Deficiency | Cabezas Syndrome | Hypoplastic Left Heart Syndrome | Down Syndrome | Dementia | Heterotopic Ossification | Spondylolisthesis | Skin Carcinoma | Benign Familial Infantile Seizures | Light Chain Amyloidosis | Lennox-Gastaut Syndrome | Seasonal Mood Disorder | Hypokalemia | Batten Disease | Wolfram Syndrome 2 | Loeys-Dietz Syndrome | Scleritis | Chondroma | Macular Degeneration | Epilepsy, Generalized | Leukocyte Adhesion Deficiency Type 1 | Autoimmune Polyendocrinopathy Syndrome Type I | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Schindler Disease | Infantile Refsum Disease | Sengers Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Hypokalemic Periodic Paralysis | Stomatitis | Autoimmune Disease | Thanatophoric Dysplasia | Cryptosporidiosis | Uveitis | Stromal Corneal Dystrophy | Compartment Syndrome | Liver Failure | Meleda Disease | Progressive Myoclonic Epilepsy | Limb Girdle Muscular Dystrophy | Pelvic Inflammatory Disease | Renal Medullary Carcinoma | Familial Glucocorticoid Deficiency | Hypertension, Renal | Cerebrovascular Disorders | Hypoglycemia | Pulmonary Alveolar Microlithiasis | Gestational Trophoblastic Disease | Sulfite Oxidase Deficiency | Congenital Hypofibrinogenemia | Heart Block | Hyperparathyroidism, Primary | Borderline Personality Disorder | Corticobasal Syndrome | Distal Myopathy 2 | Acanthosis Nigricans | Congenital Diaphragmatic Hernia | Neurofibroma, Plexiform | Transcobalamin Deficiency | Leiomyosarcoma | Autosomal Recessive Bestrophinopathy | Chromosome 16p11.2 Deletion Syndrome | CDKL5 Deficiency Disorder | Keloid | Atelosteogenesis Type 2 | Meconium Ileus | Huntington's Disease-like 2 | Episodic Ataxia | GAPO Syndrome | Congenital Mirror Movements | Gastrointestinal Disorders | Usher Syndrome Type IIC | Gout | Porokeratosis | Bronchitis | Osteoporosis | Antisynthetase Syndrome | Wolff-Parkinson-White Syndrome | Charcot-Marie-Tooth Disease Type 4E | Hyperoxaluria | Ectodermal Dysplasia | Congenital Bile Acid Synthesis Defect | Monilethrix | Eating Disorder | Adenomatoid Tumor | Hereditary Elliptocytosis | Panniculitis | Spitzoid Melanoma | Spastic Paraplegia Type 7 | Lattice Corneal Dystrophy Type 1 | Hepatitis C, Chronic | Spinocerebellar Ataxia Type 13 | Avellino Corneal Dystrophy | Babesiosis | Barakat Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Fucosidosis | Cousin Syndrome | Tuberculosis | Enlarged Vestibular Aqueduct | Pilomatrix Carcinoma | Van Der Knaap Disease | Centronuclear Myopathy | HUPRA Syndrome | Cataract | Gynecomastia | Rolandic Epilepsy | Sleep Apnea | Becker Muscular Dystrophy | Spasticity | Ellis-Van Creveld Syndrome | Metatropic Dysplasia | Keratocystic Odontogenic Tumor | Rhinitis | Ollier Disease | Familial Hypobetalipoproteinemia | Mumps | Vitreoretinal Degeneration, Snowflake Type | Fanconi Anemia | Spinocerebellar Ataxia Type 21 | Heimler Syndrome | Myhre Syndrome | Aplastic Anemia | Combined Pituitary Hormone Deficiency | Bronchiectasis | Carcinoma, Transitional Cell | Withdrawal Syndrome | Metabolic Diseases | Chronic Idiopathic Myelofibrosis | Gastric Atrophy | Epidermolytic Palmoplantar Keratoderma | Myopathy | Low Tension Glaucoma | Nemaline Myopathy 8 | KBG Syndrome | Enterocolitis, Necrotizing | Gastritis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Skin Fragility-woolly Hair Syndrome | Graft-versus-host Disease | Glutaric Aciduria Type 1 | Congenital Heart Block | Prune Belly Syndrome | Proteus Syndrome | Situs Inversus | Heart Septal Defects | Congenital Absence Of Vas Deferens | Keratosis | Neuroma | Kabuki Syndrome 2 | Birt-Hogg-Dube Syndrome | Cellulitis | Long QT Syndrome Type 1 | Paraganglioma | Parkinson's Disease