Disease

Infantile Liver Failure Syndrome 1

About the Disease
Infantile Liver Failure Syndrome 1, also known as acute infantile liver failure-multisystemic involvement syndrome, is related to infantile liver failure syndrome and liver failure, infantile, transient, and has symptoms including seizures An important gene associated with Infantile Liver Failure Syndrome 1 is LARS1 (Leucyl-TRNA Synthetase 1), and among its related pathways/superpathways are Regulation of expression of SLITs and ROBOs and tRNA Aminoacylation. The drugs Entecavir and Lenograstim have been mentioned in the context of this disorder. Affiliated tissues include liver, bone marrow and brain, and related phenotypes are frontal bossing and sensorineural hearing impairment

Common Targets
LARS1

疾病靶点研报
Infantile liver failure syndrome 1

Note: If you'd like to get a target analysis report for Infantile Liver Failure Syndrome 1, 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 Infantile Liver Failure Syndrome 1 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

Other Diseases

Pontocerebellar Hypoplasia | Dystonia | Alstrom Syndrome | Uterine Leiomyoma | Neuromuscular Disorders | Metachondromatosis | Epithelial-myoepithelial Carcinoma | Holt-Oram Syndrome | Mannosidase Deficiency Diseases | Diffuse Mesangial Sclerosis | Leukoplakia, Oral | Usher Syndrome Type III | Plasmacytoma | T-cell Prolymphocytic Leukemia | N-acetylglutamate Synthase Deficiency | Persistent Fetal Circulation | Diabetic Macular Edema | Asthma | Systemic Mastocytosis | Ornithine Transcarbamylase Deficiency | Personality Disorders | Proteus Syndrome | Pseudohermaphroditism | Adult Polyglucosan Body Disease | Basal Ganglia Disease, Biotin-responsive | Hypogammaglobulinemia | Pseudohypoparathyroidism Type 1A | Genee-Wiedemann Syndrome | Papillorenal Syndrome | Oligoastrocytoma | Infertility | Paternal Uniparental Disomy Of Chromosome 14 | Peripheral T-cell Lymphoma | Sialidosis Type I | Wiedemann-Steiner Syndrome | Diabetic Nephropathy | Kleine-Levin Syndrome | Dysthymia | Cocaine-Related Disorders | Familial Thoracic Aortic Aneurysm | Ulcerative Colitis | Muscle Wasting | Senior-Loken Syndrome | Osteoarthritis | Brooke-Spiegler Syndrome | Narcolepsy | Congenital Stationary Night Blindness | Hypercalciuria | Primary Hyperoxaluria Type 3 | Non-epidermolytic Palmoplantar Keratoderma | Choroideremia | Cataplexy | Thrombophlebitis | Crouzon Syndrome With Acanthosis Nigricans | Joubert Syndrome | Wiskott-Aldrich Syndrome | Colitis, Microscopic | Pemphigoid | Congenital Myopathy | Melanoma | Epidermolysis Bullosa | Cluster Headache | Fibromuscular Dysplasia | Rotor Syndrome | Familial Male-limited Precocious Puberty | Diabetes Insipidus, Neurogenic | Hypermethioninemia | Early Infantile Epileptic Encephalopathy 4 | Light Chain Amyloidosis | Prediabetes | Lissencephaly 2 | Congenital Muscular Dystrophy | Schwannoma | Renal Tubular Dysgenesis | Adrenal Insufficiency | Gastritis | Galloway-Mowat Syndrome | Gardner Syndrome | Periventricular Nodular Heterotopia | Recurrent Respiratory Papillomatosis | Bronchitis, Chronic | Peeling Skin Syndrome Type B | Glucagonoma | Sponastrime Dysplasia | Warsaw Breakage Syndrome | Hereditary Coproporphyria | Congenital Afibrinogenemia | Infantile Liver Failure Syndrome 1 | Polycythemia | Obesity, Morbid | Schnyder Crystalline Corneal Dystrophy | Combined Pituitary Hormone Deficiency | Hereditary Spherocytosis | Oligospermia | Thrombotic Microangiopathy | Urticaria | PASLI Disease | Hemorrhoids | Parapsoriasis | DRESS Syndrome | Connective Tissue Disorders | Hypocalcemia | Primary Hyperoxaluria | Ichthyosis | Hemolytic Uremic Syndrome | Schizophrenia | Dyggve-Melchior-Clausen Disease | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Neutropenia | Rift Valley Fever | Chiari Malformation Type I | Smith-Lemli-Opitz Syndrome | Cryptorchidism | Congenital Poikiloderma | Basan Syndrome | Hypertelorism | Cavitary Optic Disc Anomalies | Thyroid Dyshormonogenesis | Melanoma, Uveal | Diarrhea | Pure Autonomic Failure | Leukodystrophies | Fabry's Disease | Angina Pectoris | Hyper IgE Syndrome | Aspartylglycosaminuria | Patent Ductus Arteriosus | Axenfeld-Rieger Syndrome | Pneumoconiosis | Tetanus | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hypoproteinemia, Hypercatabolic | Mitochondrial DNA Depletion Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Coronary Artery Disease | Hypolipoproteinemia | Pleomorphic Xanthoastrocytoma | Esophageal Adenocarcinoma | Pulmonary Vein Stenosis | Congenital Central Hypoventilation Syndrome | Proopiomelanocortin Deficiency | Keratoconus | Ghosal Syndrome | Histiocytosis | Bartsocas-Papas Syndrome | Chondrosarcoma | Pemphigus | Tangier Disease | Sotos Syndrome | CHARGE Syndrome | Otopalatodigital Syndrome Type 2 | Spasticity | Crohn's Disease | Cannabis Abuse | Spinocerebellar Ataxia Type 8 | Retinoblastoma | Reticular Dysgenesis | Calcium Pyrophosphate Deposition Disease | Nephrosclerosis | Cutaneous T-cell Lymphoma | Familial Pheochromocytoma-paraganglioma | Glomerulonephritis, Membranoproliferative | Hypoparathyroidism | Congenital Adrenal Hyperplasia | Nijmegen Breakage Syndrome | Hypertension, Portal | Sporadic Hemiplegic Migraine | Sporadic Inclusion Body Myositis | Chorea | Endometrial Hyperplasia | Partington Syndrome | Allergic Contact Dermatitis | Combined Deficiency Of Factor V And Factor VIII | Aspergillosis | Bloom Syndrome | Diabetes Insipidus | Centronuclear Myopathy | Benign Familial Infantile Seizures | Basal Ganglia Disease | Niemann-Pick Disease | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Osteochondroma | Low Tension Glaucoma | Leishmaniasis, Cutaneous | Sengers Syndrome | Hemolytic Uremic Syndrome, Atypical | Pseudohypoparathyroidism Type 1B | Cantu Syndrome | Azoospermia | Hyperuricemia | Chronic Beryllium Disease | Hypersensitivity | Lennox-Gastaut Syndrome | Fontaine Progeroid Syndrome | Melanocytic Nevus | Smoldering Myeloma | Familial Retinal Arterial Macroaneurysm | Growth Hormone Excess | Cholecystitis | Cancer, Breast | Maternally Inherited Diabetes And Deafness | Jacobsen Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Schizophrenia, Paranoid | Hereditary Neuropathy With Liability To Pressure Palsies | Porphyria, Variegate | Focal Cortical Dysplasia Type 2 | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Papilledema | Sandhoff Disease | Congenital Torticollis | Tetraplegia | Cardiomyopathy, Dilated, 1L | Glycogen Storage Disease Type 5 | Hyperacusis | Pearson Syndrome | Pain | Hashimoto Thyroiditis | Pregnancy, Ectopic | Liddle Syndrome | Enlarged Vestibular Aqueduct | Glaucomatocyclitic Crisis | Congenital Generalized Lipodystrophy | Methylmalonic Acidemia | Proctitis | Turner's Syndrome | Pulmonary Sclerosing Hemangioma | Clouston Hidrotic Ectodermal Dysplasia | Spondylosis | Adenoma, Villous | Ellis-Van Creveld Syndrome | Mastitis | Brugada Syndrome 1 | Donnai-Barrow Syndrome | Acute Anterior Uveitis | Speech Disorders | Infantile Neuroaxonal Dystrophy | Liver Failure | Mitochondrial DNA Depletion Syndrome 13 | Schwannomatosis | Hepatitis, Chronic | Central Core Disease | Wolcott-Rallison Syndrome | Thyroiditis | Charcot-Marie-Tooth Disease, Type 1A | CREST Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Neuroblastoma | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Endometritis | Neurofibromatosis-Noonan Syndrome | Eosinophilia | Postaxial Polydactyly | X-linked Acrogigantism | Non-Hodgkin Lymphoma | Acrodysostosis | Multiple Myeloma | Galactosialidosis | Harlequin Ichthyosis | Long QT Syndrome Type 3 | Sialidosis | Diffuse Palmoplantar Keratoderma | 3-methylglutaconic Aciduria Type IV | Spinocerebellar Ataxia Type 3 | Hypermetropia | Ovarian Sex Cord-stromal Tumor | Spinal Muscular Atrophy | Pulmonary Alveolar Proteinosis | Fibromyalgia | Takenouchi-Kosaki Syndrome | Actinomycetoma | Emery-Dreifuss Muscular Dystrophy | Greig Cephalopolysyndactyly Syndrome | Hermansky-Pudlak Syndrome | Lattice Corneal Dystrophy Type 1 | Panuveitis | Ectrodactyly | Porencephaly | Hypodontia | Meier-Gorlin Syndrome | Familial Episodic Pain Syndrome | Unverricht-Lundborg Syndrome | Waardenburg Syndrome Type 2E | 3C Syndrome | DEND Syndrome | X-linked Creatine Transporter Deficiency | Hidradenitis | Chordoma | Intellectual Disability, Autosomal Dominant 5 | Kindler Syndrome | Alveolar Capillary Dysplasia | Meleda Disease | Sarcosinemia | Prurigo Nodularis | Hyperandrogenemia | Chronic Granulomatous Disease, X-linked | Epidermolytic Hyperkeratosis | Ichthyosis, X-linked | Onchocerciasis | Anorchia | Bulimia Nervosa | Intestinal Tuberculosis | Kaposiform Hemangioendothelioma | Pneumonia, Bacterial | Von Willebrand Disease | Huntington's Disease | Lassa Fever | Granuloma Annulare | Hypercholesterolemia | Acanthosis Nigricans | Sturge-Weber Syndrome | Giant Axonal Neuropathy | Micropenis | Hypereosinophilic Syndrome | Psoriasis | Pierre Robin Syndrome | Follicular Dendritic Cell Sarcoma | Cerebellofaciodental Syndrome | Central Retinal Artery Occlusion | Mast Cell Leukemia | Alopecia Areata | Peroxisomal Disorder | Intracranial Hypertension | Malignant Peripheral Nerve Sheath Tumor | Patent Foramen Ovale | Spinocerebellar Ataxia Type 31 | Porphyria, Acute Intermittent | Chondromyxoid Fibroma | Mitochondrial Disease | Insulin Resistance | Dystrophy, Cone-rod | Vici Syndrome | Meconium Ileus | Disseminated Intravascular Coagulation | Communication Disorders | Waldenstrom Macroglobulinemia | Phenylketonuria | Bardet-Biedl Syndrome | Chudley-McCullough Syndrome | Heart Septal Defects | Still Disease | Thyroid Dysgenesis | Bethlem Myopathy | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Pleural Tuberculosis | Diabetes | Charcot-Marie-Tooth Disease, Type 2C | Arts Syndrome | Dementia | Cancer, Bladder | Progressive Encephalopathy-optic Atrophy Syndrome | Brachydactyly | CDKL5 Deficiency Disorder | MELAS Syndrome | Neurodevelopmental Disorders | Acute Chest Syndrome | Megaloblastic Anemia | Danon Disease | Schuurs-Hoeijmakers Syndrome | Hyperbilirubinemia, Neonatal | Major Depression | Impetigo | Platelet Disorders | Generalized Epilepsy With Febrile Seizures Plus | Epithelioid Hemangioma | Pemphigus Vulgaris | Osteitis | Hemophagocytic Lymphohistiocytosis | Pre-eclampsia | Hypotrichosis | Osteogenesis Imperfecta Type I | Fanconi Syndrome | Loeys-Dietz Syndrome | Cancer, Prostate | Angiodysplasia | Toxoplasmosis | Meningococcal Infections | Wolff-Parkinson-White Syndrome | Ventricular Septal Defect | Gastroenteritis | Congenital Aniridia | Gerstmann-Straussler-Scheinker Syndrome | Lentigo | Medulloblastoma | Takayasu's Arteritis | Antisocial Personality Disorder | Alpers Syndrome | Feingold Syndrome | IMAGe Syndrome | Hemolytic Anemia | Graves Disease | Paraplegia | Myelomeningocele | Ovarian Hyperstimulation Syndrome | Mountain Sickness | Amish Infantile Epilepsy Syndrome | Rickets | Persistent Truncus Arteriosus | Angiosarcoma Of The Breast