Disease

Transcobalamin Deficiency

About the Disease
Transcobalamin Ii Deficiency, also known as tcn2 deficiency, is related to pancytopenia and glossitis, and has symptoms including diarrhea, lethargy and vomiting. An important gene associated with Transcobalamin Ii Deficiency is TCN2 (Transcobalamin 2), and among its related pathways/superpathways are Metabolism and Disease. Affiliated tissues include bone marrow, bone and kidney, and related phenotypes are abnormality of chromosome stability and methylmalonic aciduria

Common Targets
CD320 | TCN2

疾病靶点研报
Transcobalamin Deficiency

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

Other Diseases

Viral Meningitis | Leukoplakia | Cholelithiasis | Sleep Apnea, Obstructive | Pseudohermaphroditism | Birt-Hogg-Dube Syndrome | Adenocarcinoma | Endometritis | Becker Muscular Dystrophy | Raine Syndrome | Preaxial Polydactyly | SAPHO Syndrome | Osteochondroma | Ornithine Transcarbamylase Deficiency | Meningioma | Delayed Sleep Phase Syndrome | Persistent Fetal Circulation | Hypermetropia | Neurofibroma, Plexiform | Tularemia | Chondroma | Noonan Syndrome-like Disorder With Loose Anagen Hair | Renal Dysplasia | Congenital Nephrotic Syndrome | Congenital Heart Block | HANAC Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Brugada Syndrome 1 | Isobutyryl-CoA Dehydrogenase Deficiency | Splenomegaly | Rickets | Senior-Loken Syndrome | Porphyria, Variegate | Ocular Surface Squamous Neoplasia | Malignant Peripheral Nerve Sheath Tumor | Dermatomyositis | Ataxia-ocular Apraxia 2 | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Herpes Genitalis | Specific Granule Deficiency | Johanson-Blizzard Syndrome | Albinism | Craniosynostosis | Williams Syndrome | Kearns-Sayre Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Esophagitis | Premenstrual Syndrome | Hemoglobinopathies | Congenital Central Hypoventilation Syndrome | Ischemia | Cholestasis, Intrahepatic | Wolfram Syndrome 2 | Familial Hyperaldosteronism | Chronic Lymphocytic Leukemia | Keratoconjunctivitis | Asphyxia Neonatorum | Nance-Horan Syndrome | Usher Syndrome Type I | Diabetic Encephalopathy | Barakat Syndrome | Spinal Muscular Atrophy Type 2 | Erdheim-Chester Disease | Prolidase Deficiency | Myeloid Leukemia | Smith-Magenis Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Myoclonic Atonic Epilepsy | Epidermodysplasia Verruciformis | Hyperparathyroidism | Stickler Syndrome | Autosomal Recessive Spastic Paraplegia Type 75 | Osteogenesis Imperfecta Type I | Craniofacial Dysostosis | Avellino Corneal Dystrophy | Cerebral Amyloid Angiopathy | Hydrops Fetalis | Agoraphobia | Hepatitis D | Blau Syndrome | Familial Episodic Pain Syndrome | Unverricht-Lundborg Syndrome | Hydrocephalus, Normal Pressure | Pernicious Anemia | Filariasis | Leukoplakia, Oral | Neuronal Ceroid Lipofuscinosis | Thromboembolism | Metaphyseal Chondrodysplasia, Schmid Type | Cold Agglutinin Disease | T-cell Chronic Lymphocytic Leukemia | Hyperphenylalaninemia | Meningioma, Benign | Congenital Dyserythropoietic Anemia Type 4 | Macular Degeneration | Persistent Truncus Arteriosus | Leukocyte Adhesion Deficiency Type 1 | Majeed Syndrome | Sleep Disorder | Waldenstrom Macroglobulinemia | Cholangiocarcinoma | Snyder-Robinson Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Erythromelalgia | Intracranial Hypertension | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Enhanced S-cone Syndrome | Micro Syndrome | Lymphedema-distichiasis Syndrome | Fahr Disease | Sialidosis | Myelomeningocele | TARP Syndrome | Cryopyrin-associated Periodic Syndromes | Insulin Resistance | Lysosomal Acid Lipase Deficiency | Erythropoietic Protoporphyria | Central Pain Syndrome | Encephalopathy | Malnutrition | Juvenile Hyaline Fibromatosis | Wagner Disease | Familial Isolated Hyperparathyroidism | Reflex Epilepsy | Aldosterone Deficiency | Cerebellofaciodental Syndrome | Tatton-Brown-Rahman Syndrome | Dominant Optic Atrophy | Down Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Glycogen Storage Disease Type 0, Muscle | Camurati-Engelmann Disease | Congenital Tufting Enteropathy | C3 Glomerulopathy | Centronuclear Myopathy | Coffin-Siris Syndrome | Lichen Planus | Globozoospermia | Neuroblastoma | Hypertrophy | Stiff-man Syndrome | Gastritis, Atrophic | Spinocerebellar Ataxia Type 20 | Combined Deficiency Of Factor V And Factor VIII | Urticaria | Nutrition Disorders | Coronary Heart Disease | Best Macular Dystrophy | Esophageal Motility Disorders | Amenorrhea | Erythrokeratodermia Variabilis | Insulinoma | Diastrophic Dysplasia | Hypercholesterolemia, Familial | Acute Leukemia | Beta-Propeller Protein-associated Neurodegeneration | Angioedema | Melanocytic Nevus | Wieacker-Wolff Syndrome | Lipoma | Congenital Dyserythropoietic Anemia | Hydrocephalus | Eosinophilic Asthma | Essential Fructosuria | Granular Corneal Dystrophy Type 1 | Keratitis-ichthyosis-deafness Syndrome | Myelitis, Transverse | Ovarian Sex Cord-stromal Tumor | Congenital Absence Of Vas Deferens | Acanthosis Nigricans | Diabetes | Rubinstein-Taybi Syndrome | Glanzmann Thrombasthenia | Pterygium | Orotic Aciduria | Scleroderma | Heart Block | Histoplasmosis | Vulvovaginitis | Progressive Myoclonic Epilepsy | Aphasia | Choroiditis | Celiac Disease | Asthma, Nocturnal | Guttate Psoriasis | Autonomic Nervous System Disorders | Hoyeraal-Hreidarsson Syndrome | Glomerulonephritis, Membranoproliferative | Osteonecrosis Of The Jaw | Polyomavirus Nephropathy | Tyrosine Hydroxylase Deficiency | Acrodermatitis | Niemann-Pick Disease | Anorchia | Cornelia De Lange Syndrome | 3C Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Hyperferritinemia-cataract Syndrome | C3 Glomerulonephritis | Plasma Cell Dyscrasia | Pigment Dispersion Syndrome | Hyperkeratosis | Hemolytic Uremic Syndrome | Congenital Torticollis | Low Tension Glaucoma | Takayasu's Arteritis | Acral Lentiginous Melanoma | FG Syndrome | Steel Syndrome | Diffuse Palmoplantar Keratoderma | Batten Disease | Tardive Dyskinesia | Rift Valley Fever | Paroxysmal Nocturnal Hemoglobinuria | Pantothenate Kinase-associated Neurodegeneration | Coenzyme Q10 Deficiency | Gitelman Syndrome | Metanephric Adenoma | Azoospermia | Frontotemporal Dementia | Sertoli Cell-only Syndrome | Carcinoma, Squamous Cell | Alazami Syndrome | AIDS Dementia Complex | Persistent Hyperplastic Primary Vitreous | Bartter Syndrome | Neurogenic Bladder | Imerslund-Grasbeck Syndrome | Lentigo | Inflammatory Linear Verrucous Epidermal Nevus | Megaloblastic Anemia | Restless Legs Syndrome | Hereditary Elliptocytosis | Uveitis, Anterior | Hypokalemic Periodic Paralysis | Polymicrogyria | Cohen Syndrome | Familial Glucocorticoid Deficiency | Cancer, Lung | Cold-induced Sweating Syndrome | Hypervalinemia | Transthyretin-related Amyloidosis | Sleep Apnea | Keratosis, Actinic | Hypobetalipoproteinemias | Rheumatic Heart Disease | Malaria, Cerebral | Dermatitis Herpetiformis | Neuroleptic Malignant Syndrome | Dyslexia | Systemic Lupus Erythematosus | Cardiomyopathy, Peripartum | Anorectal Malformations | Hypertensive Nephropathy | Nephritis, Interstitial | Primary Progressive Nonfluent Aphasia | Familial Advanced Sleep Phase Syndrome | Proopiomelanocortin Deficiency | Hypertension, Renovascular | Craniofrontonasal Syndrome | Pseudoexfoliation Syndrome | Pityriasis Rubra Pilaris | Trichorhinophalangeal Syndrome | Neonatal Progeroid Syndrome | Thyroiditis, Autoimmune | Chronic Thromboembolic Pulmonary Hypertension | Congenital Adrenal Hyperplasia 1 | Tendinitis | Proteus Syndrome | Myelodysplasia | Waardenburg Syndrome Type 4A | Pseudohypoparathyroidism Type 1B | Distal Myopathy 2 | Pituitary Dwarfism | Osteogenesis Imperfecta Type IV | Chanarin-Dorfman Syndrome | Infantile Neuroaxonal Dystrophy | Mitochondrial Cytopathy | Glucagonoma | Carcinoma In Situ | Hepatitis C, Chronic | Myocardial Infarction | Learning Disability | Episodic Ataxia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | CDKL5 Deficiency Disorder | Lyme Disease | Obesity | Congenital Primary Aphakia | Plasma Cell Leukemia | Spitzoid Melanoma | Retinal Vasculitis | Peripheral T-cell Lymphoma | Hyperacusis | Melanoma | CEDNIK Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Gangliosidosis | Retinal Dystrophy | Autoimmune Polyendocrine Syndrome | Angioimmunoblastic T-cell Lymphoma | Tumoral Calcinosis | Polyneuropathy | Amish Infantile Epilepsy Syndrome | Hernia, Inguinal | Cramp Fasciculation Syndrome | X-linked Myotubular Myopathy | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Osteoporosis, Postmenopausal | Dystonia | Patent Foramen Ovale | Fetal And Neonatal Alloimmune Thrombocytopenia | Epidermolytic Hyperkeratosis | Primary Pigmented Nodular Adrenocortical Disease | Leri Pleonosteosis | Gerstmann-Straussler-Scheinker Syndrome | Nephropathy | Carcinoid Tumor | Angiosarcoma Of The Breast | GATA2 Deficiency | Hypokalemia | Spondylometaphyseal Dysplasia | Hemangioma | Schwannoma | Glycogen Storage Disease Type 6 | Lymphangioleiomyomatosis | Perry Syndrome | Familial Hemiplegic Migraine | Myotonia | Irritable Bowel Syndrome | Wolfram Syndrome | Achondrogenesis | Congenital Myasthenic Syndrome | Cryoglobulinemia | Epithelial-myoepithelial Carcinoma | Paraganglioma | Interstitial Lung Diseases | Vitamin B12 Deficiency | Coma | Familial Male-limited Precocious Puberty | Pneumococcal Meningitis | Congenital Stationary Night Blindness | Argininosuccinic Aciduria | Polycythemia Vera | Geleophysic Dysplasia | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Osteosarcoma | Schaaf-Yang Syndrome | Hemochromatosis | Liebenberg Syndrome | Huntington's Disease-like 2 | Vascular Calcification | Thyroid Dysgenesis | Cleidocranial Dysplasia | Oligoasthenoteratozoospermia | Posterior Polar Cataract | Schistosomiasis | Chromosome 9q34.3 Deletion Syndrome | Polymyalgia Rheumatica | Keratitis | Hyperinsulinemic Hypoglycemia | Congenital Aniridia | Osteoporosis | Neural Tube Defect | Spinocerebellar Ataxia Type 12 | Thalassemia, Beta | Salla Disease | Lennox-Gastaut Syndrome | Ligneous Conjunctivitis | Vitreoretinal Degeneration, Snowflake Type | Pitt-Hopkins Syndrome | Hypoalbuminemia | Takotsubo Cardiomyopathy | T-cell Lymphoma, Subcutaneous Panniculitis-like | Bladder Exstrophy | Adenosine Deaminase 2 Deficiency | Alopecia Areata | Cutis Laxa | Hypersensitivity Pneumonitis | Chronic Beryllium Disease | Acute Lung Injury | Pulmonary Alveolar Proteinosis | Sengers Syndrome | Sclerocornea | Basal Ganglia Disease, Biotin-responsive | Carcinoma, Transitional Cell | Alopecia Totalis | Hyperglycemia | Hemangioblastoma | Hyperhomocysteinemia | Osmotic Demyelination Syndrome | Hyperoxaluria | Ollier Disease | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Dementia | Charcot-Marie-Tooth Disease, Type 6 | Spinocerebellar Ataxia Type 6 | Carbonic Anhydrase VA Deficiency | Tay-Sachs Disease | Schamberg Disease