Disease

Hemosiderosis

About the Disease
Rare Hereditary Hemochromatosis, also known as iron overload, is related to hemochromatosis, type 5 and iron overload in africa. An important gene associated with Rare Hereditary Hemochromatosis is HFE (Homeostatic Iron Regulator), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Insulin receptor recycling. The drugs Orange and Deferasirox have been mentioned in the context of this disorder. Affiliated tissues include liver, heart and bone marrow, and related phenotypes are liver/biliary system and homeostasis/metabolism

Common Targets
APP | HNF4A | APOE

疾病靶点研报
Hemosiderosis

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

Other Diseases

Protein S Deficiency | Multiple Epiphyseal Dysplasia | Pituitary Dwarfism | Cartilage Disorders | Okihiro Syndrome | Gynecomastia | Polycystic Kidney, Autosomal Recessive | Mabry Syndrome | Autosomal Recessive Bestrophinopathy | Urolithiasis | Vogt-Koyanagi-Harada Syndrome | Spinocerebellar Ataxia Type 42 | Chordoid Glioma | Cold-induced Sweating Syndrome | Persistent Hyperplastic Primary Vitreous | Hypermethioninemia | Myelomeningocele | Anorchia | Paracoccidioidomycosis | Evans Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Presbycusis | Acne Vulgaris | Myofibrillar Myopathy | Ocular Hypertension | Antenatal Bartter Syndrome Type 1 | Thanatophoric Dysplasia Type 1 | Triple A Syndrome | Mitochondrial DNA Depletion Syndrome | Proteus Syndrome | Chromosome 16p11.2 Deletion Syndrome | Herpes Simplex Dermatitis | Myosin Storage Myopathy | Spinocerebellar Ataxia Type 23 | Congenital Aniridia | Dyskeratosis Congenita | Globozoospermia | Echinococcosis | Usher Syndrome | Giant Cell Glioblastoma | Bronchiolitis | Pulmonary Tuberculosis | Xeroderma Pigmentosum | Congenital Nystagmus | Hypocalcemia | Meningioma, Benign | Fontaine Progeroid Syndrome | Long QT Syndrome Type 1 | Myelitis, Transverse | Lewy Body Dementia | Treacher Collins Syndrome | Benign Recurrent Intrahepatic Cholestasis 1 | Rheumatoid Arthritis | Pleomorphic Xanthoastrocytoma | Peroxisomal Disorder | Pyelonephritis | Zollinger-Ellison Syndrome | Generalized Epilepsy With Febrile Seizures Plus | Mesothelioma, Malignant | Familial Thoracic Aortic Aneurysm | Otitis Media | Thyroid Dyshormonogenesis | Low Tension Glaucoma | Peritonitis | Primary Aldosteronism | Trismus-pseudocamptodactyly Syndrome | Hyperlipidemia, Familial Combined | Prolidase Deficiency | VACTERL Association | Proctitis | Erythromelalgia | Palsy, Cerebral | Hypotrichosis | Osmotic Demyelination Syndrome | Atrioventricular Septal Defect | Argininosuccinic Aciduria | Impetigo | Frontotemporal Dementia | Spinocerebellar Ataxia Type 14 | Perivascular Epithelioid Cell Tumor | NGLY1 Deficiency | Distal Spinal Muscular Atrophy | Homocystinuria | Glycogen Storage Disease Type 6 | Pancreatitis, Chronic | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Hepatitis E | Hypersensitivity Pneumonitis | Alopecia | Major Depression | Glycogen Storage Disease Type 9 | Craniofacial Dysostosis | Spinocerebellar Ataxia Type 6 | Erythema Multiforme | PHARC Syndrome | Herpes Genitalis | Atopy | Spasticity | Glycogen Storage Disease Type 1b | Acute Leukemia | Polyomavirus Nephropathy | Hyperthyroidism | Hypertriglyceridemia | Fundus Albipunctatus | Influenza | Neonatal Progeroid Syndrome | Nemaline Myopathy | Bone Marrow Necrosis | Retinal Dystrophy | Fatty Aldehyde Dehydrogenase Deficiency | Epithelioid Hemangioma | Aldosterone Synthase Deficiency | Rash | Inflammatory Myofibroblastic Tumor | Agnathia-Otocephaly Complex | Cousin Syndrome | Carcinoid Syndrome | Temporal Lobe Epilepsy | Pityriasis Rubra Pilaris | Pyloric Stenosis, Infantile Hypertrophic | Vertebrobasilar Insufficiency | Osteogenesis Imperfecta | Neuromuscular Disorders | Wolfram Syndrome | Skin Fragility-woolly Hair Syndrome | Dysfibrinogenemia | Heart Septal Defects | Dysplastic Nevus | Goiter, Nodular | Osteogenesis Imperfecta Type IV | Non-Langerhans Cell Histiocytosis | Myelitis | Allergic Contact Dermatitis | Focal Dermal Hypoplasia | Localized Scleroderma | Stomatitis | Rift Valley Fever | Tenosynovial Giant Cell Tumor | Cerebrovascular Disorders | Anorexia Nervosa | Esotropia | Periodontitis | Sarcoidosis | Tremor | Progressive Familial Intrahepatic Cholestasis Type 2 | Emery-Dreifuss Muscular Dystrophy | Vitamin B12 Deficiency | Nephritis, Interstitial | Portal Vein Thrombosis | Hydrolethalus Syndrome | Blepharo-cheilo-odontic Syndrome | Dengue Shock Syndrome | Non-small Cell Lung Cancer | Nicotine Addiction | Pilomatrix Carcinoma | Ocular Albinism Type 1 | Hemolytic Uremic Syndrome | Cold Agglutinin Disease | Spondyloepiphyseal Dysplasia Tarda, X-linked | Cancer, Bladder | Metabolic Syndrome | Early Infantile Epileptic Encephalopathy 28 | Epidermolytic Hyperkeratosis | Pelvic Inflammatory Disease | Micro Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Usher Syndrome Type III | Carcinoma, Squamous Cell | Sialoadenitis | Macrophagic Myofasciitis | Gastroenteritis, Eosinophilic | Adenoid Cystic Carcinoma | Endometriosis | Spondylometaphyseal Dysplasia | Congenital Diaphragmatic Hernia | Chronic Kidney Disease | Gaucher Disease | Pelizaeus-Merzbacher Disease | Ophthalmia, Sympathetic | Systemic Lupus Erythematosus | Anodontia | Hypoparathyroidism | Chanarin-Dorfman Syndrome | Pontocerebellar Hypoplasia Type 7 | Citrullinemia | Sepiapterin Reductase Deficiency | Cancer, Breast | Rotor Syndrome | Oligoastrocytoma | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Coma | Lattice Corneal Dystrophy Type 1 | Melanocytic Nevus | Oculocutaneous Albinism | Hereditary Sensory And Autonomic Neuropathy | Growth Hormone Excess | Alkaptonuria | Woodhouse-Sakati Syndrome | Glycogen Storage Disease | Papilloma | Dent Disease | Benign Familial Pemphigus | Partington Syndrome | Hereditary Xerocytosis | Melanoma, Malignant | Agoraphobia | Sarcoma, Alveolar Soft Part | Neurocutaneous Syndromes | Brachydactyly | Hypertrophy | Hyperostosis | Tylosis With Esophageal Cancer | Arthropathy | Aarskog-Scott Syndrome | Reticular Dysgenesis | Hypersomnia | Scabies | Seborrheic Dermatitis | Conjunctivitis, Allergic | Sengers Syndrome | Hypophosphatasia | Porencephaly | Thrombotic Microangiopathy | Hyperkalemic Periodic Paralysis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Charcot-Marie-Tooth Disease Type 4E | Fetal Akinesia Deformation Sequence | Glaucoma, Congenital | Congenital Stationary Night Blindness | DEND Syndrome | Gliosarcoma | Pancytopenia | Osteosarcoma | Niemann-Pick Disease, Type A | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Castleman Disease | TARP Syndrome | Angiosarcoma Of The Breast | Albinism | Primary Progressive Nonfluent Aphasia | Microcephalic Primordial Dwarfism | Blue Nevus | POEMS Syndrome | Panic Disorder | Tyrosine Hydroxylase Deficiency | Corneal Dystrophy | Fraser Syndrome | Angioedema, Hereditary | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | T-cell Lymphoma, Subcutaneous Panniculitis-like | Epidermodysplasia Verruciformis | Donnai-Barrow Syndrome | Demyelinating Diseases | Postpartum Depression | Charcot-Marie-Tooth Disease, Type 1A | Pompe Disease | Congenital Stromal Corneal Dystrophy | Chronic Inflammatory Demyelinating Polyneuropathy | Oculopharyngeal Muscular Dystrophy | Vascular Calcification | Thalassemia | Disseminated Superficial Actinic Porokeratosis | Low Phospholipid Associated Cholelithiasis | Hamartoma | Bronchitis | Renal Hypomagnesemia 3 | Tietze Syndrome | Charcot-Marie-Tooth Disease | Spinocerebellar Ataxia Type 21 | Adenoma, Pituitary | Chloridorrhea, Congenital | Hereditary Hemorrhagic Telangiectasia Type 2 | Schizophrenia | Polymicrogyria | Glomerulonephritis, Membranous | Autoimmune Polyendocrinopathy Syndrome Type I | Hyperthermia, Malignant | Esthesioneuroblastoma | Binge Eating Disorder | Pseudohypoparathyroidism Type 2 | Essential Fructosuria | Rosacea | Waldenstrom Macroglobulinemia | Recurrent Respiratory Papillomatosis | Clouston Hidrotic Ectodermal Dysplasia | Sarcoma | Anemia | Oculocutaneous Albinism Type 2 | Hemochromatosis | Spinal And Bulbar Muscular Atrophy | Acute Myeloid Leukemia | HANAC Syndrome | Papilledema | Eosinophilia | Congenital Disorders Of Glycosylation | Asthma, Nocturnal | Hypokalemic Periodic Paralysis | Disseminated Intravascular Coagulation | Keratocystic Odontogenic Tumor | Rhizomelic Chondrodysplasia Punctata | Schamberg Disease | Diffuse Mesangial Sclerosis | Oligoasthenoteratozoospermia | Methemoglobinemia | Polycystic Liver | Ectrodactyly | Hidradenitis | Lymphangioleiomyomatosis | Familial Male-limited Precocious Puberty | DICER1 Syndrome | Frank-ter Haar Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Carpal Tunnel Syndrome | Left Ventricular Noncompaction | Fibromuscular Dysplasia | Osteopetrosis | Compartment Syndrome | Intestinal Obstruction | Hypoplastic Left Heart Syndrome | Uterine Leiomyoma | Nance-Horan Syndrome | Epidermolysis Bullosa Simplex, Localized | Pantothenate Kinase-associated Neurodegeneration | Ectopia Lentis, Isolated, Autosomal Recessive | Intermittent Claudication | Infertility | Schwannomatosis | Cyst | Conduct Disorder | Pyruvate Carboxylase Deficiency Disease | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Waardenburg Syndrome Type 1 | Wolfram Syndrome 2 | Meniere's Disease | Charcot-Marie-Tooth Disease Type 2D | Primary Torsion Dystonia | Oculodentodigital Dysplasia | Osteonecrosis | Polydactyly | Priapism | Anthrax | Schuurs-Hoeijmakers Syndrome | Optic Nerve Diseases | Congenital Poikiloderma | Protein C Deficiency | Glaucomatocyclitic Crisis | Malaria, Cerebral | Dermatitis Herpetiformis | 3-methylglutaconic Aciduria | Autosomal Recessive Congenital Ichthyosis | Menetrier Disease | Biotinidase Deficiency | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Sleep Disorder | Phenylketonuria | Cholangitis | Spinal Muscular Atrophy Type 3 | Neurocysticercosis | Neuroendocrine Cancer | Ureteropelvic Junction Obstruction | Uremia | Guanidinoacetate Methyltransferase Deficiency | Stickler Syndrome | Hypertension, Renovascular | Glycogen Storage Disease Type 3 | Schizencephaly | Familial Exudative Vitreoretinopathy | Congenital Primary Aphakia | Bursitis | Antisocial Personality Disorder | FG Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Viral Meningitis | Takayasu's Arteritis | Meningitis | Osteoporosis-pseudoglioma Syndrome | Alexander Disease | Iron Metabolism Disorders | Dysgerminoma | Erectile Dysfunction | Maternally Inherited Diabetes And Deafness | Idiopathic Multicentric Castleman Disease | Hereditary Sensory Neuropathy Type 1 | T-cell Prolymphocytic Leukemia | Ovarian Sex Cord-stromal Tumor | Lipodystrophy | Trigonocephaly | Myasthenia Gravis | Oral Lichen Planus | Renal Dysplasia | Pulmonary Alveolar Microlithiasis | Porphyria, Variegate | Glutathione Synthetase Deficiency | Carotid Artery Disease | Charcot-Marie-Tooth Disease Type 3 | Brooke-Spiegler Syndrome | Pain | Rhabdomyosarcoma, Embryonal | Nemaline Myopathy 8 | Kaposiform Hemangioendothelioma