Disease

Methemoglobinemia Type IV

About the Disease
Methemoglobinemia and Ambiguous Genitalia, also known as methemoglobinemia type iv, is related to methemoglobinemia and congenital methemoglobinemia. An important gene associated with Methemoglobinemia and Ambiguous Genitalia is CYB5A (Cytochrome B5 Type A), and among its related pathways/superpathways is "Methylene Blue Pathway, Pharmacodynamics". Related phenotypes are micropenis and bifid scrotum

Common Targets
CYB5R3

疾病靶点研报
Methemoglobinemia Type IV

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

Other Diseases

Pemphigus Foliaceus | Myoclonic Atonic Epilepsy | Trachoma | Niemann-Pick Disease | Duchenne Muscular Dystrophy | Systemic Mastocytosis | Pigment Dispersion Syndrome | Methylmalonic Acidemia | Lattice Corneal Dystrophy Type 1 | Orthostatic Intolerance | Neurofibromatosis Type 1 | Gastroschisis | Rhabdomyosarcoma | Pseudohermaphroditism | Sengers Syndrome | Schistosomiasis | Phenylketonuria | Disseminated Intravascular Coagulation | Osteomyelitis | Schaaf-Yang Syndrome | Osteopetrosis | Congenital Tufting Enteropathy | Enhanced S-cone Syndrome | Microphthalmia | Roberts Syndrome | Rash | Hepatitis | Malignant Peripheral Nerve Sheath Tumor | Alzheimer Disease, Late Onset | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Cryoglobulinemia | Dystonia Musculorum Deformans | Pneumococcal Meningitis | Spinocerebellar Ataxia Type 5 | Benign Familial Infantile Seizures | Pancytopenia | Carcinoma, Small Cell | Brooke-Spiegler Syndrome | Spitzoid Melanoma | Glycogen Storage Disease Type 5 | Arts Syndrome | Paraplegia | Sleep Apnea, Central | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Skin Papilloma | Waardenburg Syndrome Type 1 | Ependymoma | Cholesteryl Ester Storage Disease | Astrocytoma, Anaplastic | Cardiac Sarcoidosis | Infantile Spasm | Kleine-Levin Syndrome | Membranous Nephropathy | Greenberg Dysplasia | Proteasome-associated Autoinflammatory Syndrome 2 | Extramammary Paget's Disease | Aphasia | Cataplexy | Obesity, Morbid | Nijmegen Breakage Syndrome | Porphyria, Variegate | Giant Cell Glioblastoma | Ollier Disease | Neurodermatitis | Hyperbilirubinemia, Neonatal | Cervicitis | Spinocerebellar Ataxia Type 12 | Stickler Syndrome | Jalili Syndrome | Epicondylitis | Hydronephrosis | Pneumothorax | Hyper IgE Syndrome | Micro Syndrome | Diastrophic Dysplasia | Rotor Syndrome | Myelitis, Transverse | Glioma | ADNP Syndrome | Intestinal Obstruction | Thrombocythemia, Essential | Brugada Syndrome 1 | Waardenburg Syndrome Type 2A | Otosclerosis | Epidermolysis Bullosa | Burn-McKeown Syndrome | Neurocutaneous Syndromes | Glycogen Storage Disease Type 1b | Thyroiditis | Meconium Ileus | Spondyloperipheral Dysplasia | Basal Ganglia Disease, Biotin-responsive | B-cell Prolymphocytic Leukemia | Blue Rubber Bleb Nevus Syndrome | Fibrodysplasia Ossificans Progressiva | DOCK8 Immunodeficiency Syndrome | Hodgkin Lymphoma | Cholecystitis | Astigmatism | Adams-Oliver Syndrome | Panic Disorder | Benign Recurrent Intrahepatic Cholestasis 1 | Brachial Plexus Neuropathy | Pulmonary Veno-occlusive Disease | Fetal Alcohol Syndrome | Methemoglobinemia Type IV | Craniofacial Dysostosis | Alopecia Totalis | Glycogen Storage Disease Type 0 | Charcot-Marie-Tooth Disease Type 4D | Spinocerebellar Ataxia Type 27 | Huntington's Disease-like 2 | Renal-hepatic-pancreatic Dysplasia | Scapuloperoneal Spinal Muscular Atrophy | Spondyloepiphyseal Dysplasia Tarda, X-linked | Trigonocephaly | Fuchs Dystrophy | Raynaud Phenomenon | Acne | Retinoschisis | Werner's Syndrome | Pleural Tuberculosis | Olmsted Syndrome | Cystinuria | Chronic Kidney Disease | Myocardial Infarction | Tinea | Urolithiasis | Hyperkalemic Periodic Paralysis | Hypermethioninemia | Oculopharyngeal Muscular Dystrophy | Mandibuloacral Dysplasia With Type A Lipodystrophy | Skin Carcinoma | Diabetes | Parkinson Disease 6, Autosomal Recessive Early-onset | Gangliosidosis, GM1 | Gastric Atrophy | Congenital Muscular Dystrophy | Osteomalacia | Optic Neuritis | Low Phospholipid Associated Cholelithiasis | Adenylosuccinate Lyase Deficiency | Hartsfield Syndrome | Citrullinemia | Mixed Connective Tissue Disease | Hypogonadism | Chondromyxoid Fibroma | Amelanotic Melanoma | Arthrogryposis | Epidermolytic Hyperkeratosis | Myofibromatosis | Myopathy | Acute Lymphocytic Leukemia | Silicosis | Primary Familial Brain Calcification | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Melanocytic Nevus | Donnai-Barrow Syndrome | Cannabis Abuse | Pulmonary Tuberculosis | Shock, Cardiogenic | Cancer, Breast | Epidermolysis Bullosa Simplex, Generalized | Chronic Granulomatous Disease | Retinal Diseases | Hydrops Fetalis | Best Macular Dystrophy | Hydrolethalus Syndrome | Papilloma | Subcortical Band Heterotopia | Insulin Resistance | Hypopigmentation | Primary Hyperoxaluria Type 1 | Hereditary Sensory And Autonomic Neuropathy | Retinopathy Of Prematurity | Tay-Sachs Disease | Primary Cutaneous Amyloidosis | Epidermolysis Bullosa Dystrophica | Congenital Fiber-type Disproportion Myopathy | Lymphangiomatosis | Colon Adenoma | Arthritis, Psoriatic | Retinopathy, Diabetic | Prolidase Deficiency | Renal Failure | Eating Disorder | Cohen Syndrome | Coloboma | Myosin Storage Myopathy | Zygomycosis | Synovitis | T-cell Chronic Lymphocytic Leukemia | Congestive Heart Failure | Menkes Disease | Thin Basement Membrane Disease | Ichthyosis, X-linked | Toxic Epidermal Necrolysis | Anxiety Disorders | Alopecia | Pouchitis | Chordoma | Traboulsi Syndrome | Retinitis | Onchocerciasis | Cyclic Vomiting Syndrome | Erdheim-Chester Disease | Hypersomnia | Infantile Refsum Disease | Thrombotic Microangiopathy | Pseudohypoparathyroidism Type 2 | Silver-Russell Syndrome | Hypertension, Renovascular | Multiple Myeloma | Pure Autonomic Failure | Adrenal Insufficiency | Coffin-Lowry Syndrome | Early Infantile Epileptic Encephalopathy 1 | Hypohidrotic Ectodermal Dysplasia | Amish Infantile Epilepsy Syndrome | Combined Deficiency Of Factor V And Factor VIII | Hypotrichosis | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | CDKL5 Deficiency Disorder | Borjeson-Forssman-Lehmann Syndrome | Placenta Previa | Postpartum Depression | Thyroid Dysgenesis | Leiomyoma | Larsen Syndrome | Neurofibroma | Usher Syndrome | Meningococcal Infections | Nicolaides-Baraitser Syndrome | Jacobsen Syndrome | Toxoplasmosis | Eosinophilia | Non-Hodgkin Lymphoma | Esotropia | Gigantism | Hereditary Hemorrhagic Telangiectasia Type 2 | Autosomal Recessive Congenital Ichthyosis | Bronchitis | Pierpont Syndrome | Glomerulonephritis, Membranoproliferative | Beare-Stevenson Syndrome | 3-methylglutaconic Aciduria | Occipital Neuralgia | Hyperacusis | Myeloid Leukemia | Heavy Chain Disease | Triphalangeal Thumb-polysyndactyly Syndrome | Asthma, Exercise-induced | Vitamin A Deficiency | Endometritis | Trichomegaly | Obsessive-compulsive Disorder | Generalized Epilepsy And Paroxysmal Dyskinesia | Persistent Mullerian Duct Syndrome | Autism | Metachromatic Leukodystrophy | Primary Progressive Nonfluent Aphasia | Tenosynovial Giant Cell Tumor | Fahr Disease | Myositis | Carey-Fineman-Ziter Syndrome | Saul-Wilson Syndrome | Celiac Disease | Fucosidosis | Congenital Dysfibrinogenemia | Aneurysm, Thoracic Aortic | Multicystic Renal Dysplasia | Cryptosporidiosis | Hypertension, Portal | Tibial Muscular Dystrophy | Common Variable Immunodeficiency | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Muscle Wasting | Monilethrix | Gingivitis | Familial Episodic Pain Syndrome | Erythrokeratodermia Variabilis | Mucolipidosis Type IV | Leukocyte Adhesion Deficiency Type 1 | Waldenstrom Macroglobulinemia | Li-Fraumeni Syndrome | Osteopathia Striata With Cranial Sclerosis | Anencephaly | Thyrotoxic Periodic Paralysis | Cenani-Lenz Syndactyly Syndrome | Antisocial Personality Disorder | Constipation | Osteitis | Overactive Bladder | Endometriosis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Chromosome 8q21.11 Deletion Syndrome | Blepharo-cheilo-odontic Syndrome | Snyder-Robinson Syndrome | Primary Lateral Sclerosis | Urea Cycle Disorder | Withdrawal Syndrome | Rhabdoid Tumor | Fragile X Syndrome | Geleophysic Dysplasia | Hypohidrotic Ectodermal Dysplasia, X-linked | Autonomic Neuropathy | Birk-Barel Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Lupus Erythematosus | Schnitzler Syndrome | Retinal Dystrophy | CHARGE Syndrome | Lissencephaly 2 | Duodenal Atresia | SAPHO Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Macular Corneal Dystrophy Type 1 | Erythematotelangiectatic Rosacea | Holt-Oram Syndrome | Usher Syndrome Type I | Mannosidase Deficiency Diseases | Thromboembolism | Hemolytic Anemia | Lipid Storage Myopathy | Sarcoma, Alveolar Soft Part | Cocaine-Related Disorders | Headache | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Cushing Syndrome | Personality Disorders | Meckel-Gruber Syndrome | CHOPS Syndrome | Language Disorders | Ataxia-ocular Apraxia 2 | Autoimmune Disease | Deafness, Dystonia, And Cerebral Hypomyelination | Batten Disease | Vascular Cognitive Impairment | Seborrheic Dermatitis | Non-Langerhans Cell Histiocytosis | Lassa Fever | Adenosine Deaminase Deficiency | Cellulitis | Herpes Genitalis | Hidradenitis | Spondylolisthesis | Uremia | Scoliosis | Hepatic Adenomatosis | Neurofibromatosis Type 2 | Walker-Warburg Syndrome | Intestinal Tuberculosis | Ichthyosis Hystrix, Curth-Macklin Type | Hemangioma | Kidney Stones | Cholangitis | Pleomorphic Xanthoastrocytoma | Dystonia-parkinsonism, X-linked | Avellino Corneal Dystrophy | Diarrhea | MIRAGE Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Myotonia | LEOPARD Syndrome | Dysmorphophobia | Acute Coronary Syndrome | Anterior Segment Dysgenesis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Trimethylaminuria | Alopecia Areata | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Neural Tube Defect | Lymphedema | Diabetic Neuropathy | Hypotrichosis Simplex | Trismus-pseudocamptodactyly Syndrome | Juvenile Xanthogranuloma | Macular Corneal Dystrophy | Inflammatory Myofibroblastic Tumor | Odonto-onycho-dermal Dysplasia | Infectious Diarrhea | Hyperostosis | Urticaria | Ovarian Sex Cord-stromal Tumor | Acute Leukemia | Intermittent Claudication | Thrombophilia | Perivascular Epithelioid Cell Tumor | Spina Bifida | Liebenberg Syndrome | Anovulation | Cancer, Prostate | Uterine Leiomyoma | Mucormycosis | Cabezas Syndrome | Spastic Paraplegia Type 7 | Lateral Meningocele Syndrome | Coenzyme Q10 Deficiency | Rett Syndrome | Lung Diseases