Disease

Primary Hyperoxaluria Type 3

About the Disease
Hyperoxaluria, Primary, Type Iii, also known as primary hyperoxaluria type 3, is related to primary hyperoxaluria and nephrolithiasis, calcium oxalate. An important gene associated with Hyperoxaluria, Primary, Type Iii is HOGA1 (4-Hydroxy-2-Oxoglutarate Aldolase 1), and among its related pathways/superpathways are PERK regulates gene expression and Glyoxylate metabolism and glycine degradation. The drugs Omalizumab and Mupirocin have been mentioned in the context of this disorder. Affiliated tissues include kidney, pancreas and skeletal muscle, and related phenotypes are hematuria and nephrocalcinosis

Common Targets
HOGA1

疾病靶点研报
Primary Hyperoxaluria Type 3

Note: If you'd like to get a target analysis report for Primary Hyperoxaluria Type 3, 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 Primary Hyperoxaluria Type 3 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Lactose Intolerance | Fibrosis | Silver-Russell Syndrome | Coloboma | Thrombocythemia, Essential | Diabetic Macular Edema | Kabuki Syndrome 2 | Chorea-acanthocytosis | Cystinosis | Cleidocranial Dysplasia | Glycogen Storage Disease Type 5 | Gout | Malaria, Cerebral | Renal Failure | Spinocerebellar Ataxia Type 13 | Anodontia | Rett Syndrome | Alpha-mannosidosis | Evans Syndrome | Meningioma, Benign | Fuchs Dystrophy | Myelitis, Transverse | Renal Hypomagnesemia 3 | Stevens-Johnson Syndrome | Goiter | Birk-Barel Syndrome | Congenital Hypofibrinogenemia | Nephronophthisis | Parvovirus B19 Infection | Tumoral Calcinosis | Twin-to-twin Transfusion Syndrome | Lyme Disease | Aneurysm, Abdominal Aortic | Cirrhosis | Panuveitis | Hemorrhoids | Epidermolytic Palmoplantar Keratoderma | Lipid Storage Myopathy | Cerebral Amyloid Angiopathy | DRESS Syndrome | Inflammatory Myofibroblastic Tumor | Basal Ganglia Disease, Biotin-responsive | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Hypertelorism | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Coenzyme Q10 Deficiency | Charcot-Marie-Tooth Disease, Type 1A | Tendinitis | Periodic Limb Movement Disorder | COACH Syndrome | Heterotopic Ossification | Varicocele | Cryptosporidiosis | Primary Carnitine Deficiency | Thrombosis | Ovarian Sex Cord-stromal Tumor | Malnutrition | Chylothorax, Congenital | Autonomic Neuropathy | Leukemia | Cramp Fasciculation Syndrome | Shwachman-Bodian-Diamond Syndrome | Tetraplegia | Wolfram Syndrome | Retinopathy, Diabetic | Colitis, Lymphocytic | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Schizencephaly | Non-proliferative Diabetic Retinopathy | Hepatic Adenomatosis | Tardive Dyskinesia | AIDS Dementia Complex | Hereditary Multiple Exostoses | Esophagitis, Eosinophilic | Adenylosuccinate Lyase Deficiency | Usher Syndrome Type III | Crimean-Congo Hemorrhagic Fever | Distal Spinal Muscular Atrophy | Congenital Dyserythropoietic Anemia Type 1 | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Urofacial Syndrome | Mucolipidosis Type II | Avellino Corneal Dystrophy | Bronchitis, Chronic | Relapsing Polychondritis | Spastic Paraplegia Type 7 | Benign Hereditary Chorea | Myelitis | Waardenburg Syndrome Type 1 | Synovitis | Eosinophilia | Metanephric Adenoma | Pompe Disease | Low Phospholipid Associated Cholelithiasis | Hypermethioninemia | Pernicious Anemia | Combined Pituitary Hormone Deficiency | Vitamin A Deficiency | Early Infantile Epileptic Encephalopathy 4 | Short-chain Acyl-CoA Dehydrogenase Deficiency | Hyperglycemia | Metaphyseal Chondrodysplasia, Schmid Type | Pemphigoid | Barrett Esophagus | Sarcoma, Endometrial Stromal | Lipid Metabolism Disorders | Hypotension, Orthostatic | Oculocutaneous Albinism Type 1 | Arthritis, Gouty | Hemoglobinopathies | Rotor Syndrome | Methylmalonic Acidemia | Palsy, Cerebral | Early Infantile Epileptic Encephalopathy 28 | Uveitis, Anterior | Dyslipidemia | Pre-eclampsia | Congenital Heart Block | Nicotine Dependence | Guanidinoacetate Methyltransferase Deficiency | Peroxisomal Disorder | Blepharospasm | Spinocerebellar Ataxia Type 8 | Acute Chest Syndrome | Cancer, Breast | Mucolipidosis Type IV | Spondylocarpotarsal Synostosis Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Incontinentia Pigmenti | Li-Fraumeni Syndrome | Aldosterone Synthase Deficiency | Pseudo-pseudohypoparathyroidism | Central Retinal Artery Occlusion | Cartilage Disorders | Herpes Genitalis | Mitochondrial Encephalomyopathy | Sarcoma, Ewing | Osteoporosis | Eczema | Empyema | Lymphangioleiomyomatosis | Myopia | Geleophysic Dysplasia | Acute Coronary Syndrome | Graft-versus-host Disease | Cardiomyopathy, Restrictive | Sengers Syndrome | Autosomal Recessive Bestrophinopathy | Temtamy Preaxial Brachydactyly Syndrome | Congenital Generalized Lipodystrophy | Tay-Sachs Disease | Alpha-1 Antitrypsin Deficiency | Tuberculosis | Huntington's Disease | Intracranial Hypertension | Orotic Aciduria | Leukemia-lymphoma, Adult T-cell | Disseminated Superficial Actinic Porokeratosis | Absence Epilepsy | Sleep Apnea | Pyruvate Dehydrogenase Deficiency | Heroin Dependence | Reye Syndrome | Conn Syndrome | Coffin-Lowry Syndrome | Brachial Plexus Neuropathy | Paroxysmal Kinesigenic Dyskinesia | Roberts Syndrome | Panniculitis | Epidermolysis Bullosa Simplex | Rhizomelic Chondrodysplasia Punctata | Primary Hyperoxaluria | Enlarged Vestibular Aqueduct | Perry Syndrome | Osteonecrosis Of The Jaw | Cholestasis | Parkinson's Disease | Leigh Syndrome | Kaposi Sarcoma | Bone Giant Cell Tumor | Hepatic Veno-occlusive Disease | Progressive Encephalopathy-optic Atrophy Syndrome | Intestinal Hypomagnesemia 1 | Kashin-Beck Disease | Hydronephrosis | Hoyeraal-Hreidarsson Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Hydrolethalus Syndrome | Gitelman Syndrome | Chondromyxoid Fibroma | Ocular Hypertension | Transthyretin-related Amyloidosis | Esophageal Carcinoma | Nicotine Addiction | Sponastrime Dysplasia | 5-oxoprolinase Deficiency | Spinal And Bulbar Muscular Atrophy | Sclerosteosis | Rhabdomyosarcoma, Embryonal | Amyloidosis | Acanthosis Nigricans | Infectious Diarrhea | Chondrosarcoma | Rubeosis Iridis | Hepatorenal Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Zollinger-Ellison Syndrome | MIRAGE Syndrome | Sleep Disorder | Lattice Corneal Dystrophy Type 1 | Stuve-Wiedemann Syndrome | CHOPS Syndrome | Ischemia | Microphthalmia | Epidermodysplasia Verruciformis | Anorectal Fistula | Citrullinemia | Congenital Diaphragmatic Hernia | Scleritis | Familial Episodic Pain Syndrome | Meier-Gorlin Syndrome | Richter's Syndrome | Chondrodysplasia Punctata 2, X-linked Dominant | Carcinoid Tumor | Chronic Myelomonocytic Leukemia | Hypercholesterolemia | Hemimegalencephaly | Orthostatic Intolerance | Tyrosinemia Type 2 | Congenital Stromal Corneal Dystrophy | Asperger Syndrome | Medulloblastoma | Spinocerebellar Ataxia Type 23 | Erythrokeratodermia Variabilis | Schwannoma | Craniosynostosis | Congenital Ichthyosiform Erythroderma | Pigment Dispersion Syndrome | Multiple Myeloma | Meningeal Melanocytoma | Swine Influenza | Asphyxia Neonatorum | Acne | Vulvovaginitis | Pyruvate Kinase Deficiency | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | NDH Syndrome | Carotid Artery Disease | Retinoschisis | Blue Nevus | Hypospadias | Anterior Segment Dysgenesis | Osteogenesis Imperfecta Type VI | Pulmonary Capillary Hemangiomatosis | Chronic Granulomatous Disease | Wilson's Disease | Atrioventricular Septal Defect | Hemochromatosis | Acute Kidney Injury | Krabbe Disease | Van Der Knaap Disease | Pituitary Disorders | 3-methylglutaconic Aciduria Type I | Alcoholism | Polyneuropathy | Cancer, Colon | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Mood Disorder | Optic Nerve Diseases | Astigmatism | Beta-Propeller Protein-associated Neurodegeneration | Nutrition Disorders | 3-methylglutaconic Aciduria | Sitosterolemia | Omenn Syndrome | Haim-Munk Syndrome | Heart Septal Defects | Multiple Sclerosis | Gangliosidosis, GM1 | Neurofibromatosis-Noonan Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Coronary Restenosis | Hereditary Spherocytosis | Dementia | Heterotaxy | Paternal Uniparental Disomy Of Chromosome 14 | Behavioral Variant Of Frontotemporal Dementia | Epidermolytic Ichthyosis, Annular | Thromboembolism | Scoliosis | Autosomal Recessive Spastic Paraplegia Type 75 | Iron Metabolism Disorders | Spitzoid Melanoma | Muckle-Wells Syndrome | Mountain Sickness | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Amyotrophic Lateral Sclerosis, Juvenile | Glioma | Pyoderma Gangrenosum | Thrombocytopenia | Hepatitis, Autoimmune | Knobloch Syndrome | Spondylocostal Dysostosis | Dystrophy, Cone-rod | Ataxia-ocular Apraxia 2 | Spitz Nevus | Campomelic Dysplasia | DOCK8 Immunodeficiency Syndrome | Von Hippel-Lindau Disease | Nemaline Myopathy 10 | Adenomyosis | Cholangitis | Fetal And Neonatal Alloimmune Thrombocytopenia | Juvenile Polyposis | Lymphedema | Schamberg Disease | Porphyria Cutanea Tarda | Bare Lymphocyte Syndrome | Chronic Neutrophilic Leukemia | Hypoalbuminemia | Keratitis | Canavan Disease | Familial Partial Lipodystrophy | Kernicterus | Polycystic Kidney, Autosomal Recessive | CREST Syndrome | Familial Thoracic Aortic Aneurysm | LEOPARD Syndrome | Bardet-Biedl Syndrome | Wiedemann-Steiner Syndrome | Congenital Heart Defects | Progressive Familial Intrahepatic Cholestasis Type 2 | GATA2 Deficiency | Familial Retinal Arterial Macroaneurysm | Bruck Syndrome | Fibronectin Glomerulopathy | Hypolipoproteinemia | Hepatitis C, Chronic | Erythropoietic Protoporphyria | Seminoma | Hyperbilirubinemia, Neonatal | Hereditary Sensory Neuropathy Type 1 | Retinal Dystrophy, Early-onset Severe | Charcot-Marie-Tooth Disease Type 4E | Paroxysmal Nocturnal Hemoglobinuria | Bursitis | Klippel-Feil Syndrome | Major Depression | Schwannomatosis | Epidermal Nevus Syndrome | C3 Glomerulonephritis | Hernia, Inguinal | Maternally Inherited Diabetes And Deafness | Spinocerebellar Ataxia Type 40 | Angioedema | Parapsoriasis | Acrodermatitis | Agranulocytosis | Neutropenia | Waardenburg Syndrome Type 2A | Hyperhomocysteinemia | Chronic Beryllium Disease | Tularemia | Neurofibrosarcoma | Myeloid Leukemia | Cardiomyopathy, Peripartum | Scapuloperoneal Spinal Muscular Atrophy | Neonatal Progeroid Syndrome | Schizoaffective Disorder | Neuroendocrine Cancer | Headache | Zellweger Syndrome | Hyperinsulinemic Hypoglycemia | Blastomycosis | Lymphoma, Follicular | Hereditary Sensory And Autonomic Neuropathy | Thyrotoxic Periodic Paralysis | Congenital Disorders Of Glycosylation Type II | Amebiasis | Skin Carcinoma | Pulmonary Alveolar Proteinosis | Teratozoospermia | Emery-Dreifuss Muscular Dystrophy | Neutrophilia | 3-methylcrotonyl-CoA Carboxylase Deficiency | Primary Hyperoxaluria Type 3 | Cancer, Bladder | Renal Oncocytoma | Oculocutaneous Albinism | Mandibuloacral Dysplasia With Type A Lipodystrophy | Acute Generalized Exanthematous Pustulosis | Angioimmunoblastic T-cell Lymphoma | Exotropia | Vasculitis | Hemangioendothelioma | Peripheral T-cell Lymphoma | Alazami Syndrome | Giant Axonal Neuropathy | Sturge-Weber Syndrome | Neurocutaneous Syndromes