Disease

Hypervalinemia

About the Disease
Valinemia, also known as hypervalinemia, is related to hypervalinemia and hyperleucine-isoleucinemia and hyperleucine-isoleucinemia. Related phenotypes are failure to thrive and muscle weakness

Common Targets
BCAT2

疾病靶点研报
Hypervalinemia

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

Other Diseases

Pontocerebellar Hypoplasia Type 7 | Renal Failure | Guttate Psoriasis | Reye Syndrome | Narcolepsy | 3-methylcrotonyl-CoA Carboxylase Deficiency | Avian Influenza | Metatropic Dysplasia | Lymphangioleiomyomatosis | Tietze Syndrome | Hypertension, Renovascular | Adrenomyeloneuropathy | Phosphoglycerate Dehydrogenase Deficiency | Hypotonia-cystinuria Syndrome | Vascular Calcification | Best Macular Dystrophy | Antithrombin III Deficiency | Early Infantile Epileptic Encephalopathy | Hyperlipidemia Type V | Cold Agglutinin Disease | Multiple Sclerosis, Chronic Progressive | Stuve-Wiedemann Syndrome | PASLI Disease | Plasma Cell Leukemia | Relapsing Polychondritis | Joubert Syndrome 2 | Charcot-Marie-Tooth Disease Type 4 | Hyperkalemic Periodic Paralysis | Spasticity | Potocki-Shaffer Syndrome | Spinocerebellar Ataxia Type 10 | Chromosome 8q21.11 Deletion Syndrome | Asperger Syndrome | Polymicrogyria | Bloom Syndrome | Chondroma | Trichothiodystrophy | Anodontia | Hypertension, Essential | Myeloid Leukemia | Rheumatic Heart Disease | Hyperprolactinemia | Kawasaki Disease | Sitosterolemia | Blepharoconjunctivitis | Hernia, Inguinal | Anovulation | Charcot-Marie-Tooth Disease, Type 6 | Impetigo | Varices | Corneal Dystrophies, Hereditary | Fanconi Syndrome | Neuroleptic Malignant Syndrome | Holt-Oram Syndrome | Hodgkin Lymphoma | Postpoliomyelitis Syndrome | Long QT Syndrome Type 3 | Progressive Familial Intrahepatic Cholestasis | Polymyositis | Emery-Dreifuss Muscular Dystrophy | Rhabdomyosarcoma | Encephalopathy, Hepatic | Myosin Storage Myopathy | Short-chain Acyl-CoA Dehydrogenase Deficiency | Facioscapulohumeral Muscular Dystrophy | Cholera | Inflammatory Joint Disease | Isovaleric Acidemia | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Cushing Syndrome | Osteogenesis Imperfecta Type IV | Polycythemia Vera | Patent Ductus Arteriosus | Nicotine Dependence | Premature Ejaculation | Hoyeraal-Hreidarsson Syndrome | Congenital Bile Acid Synthesis Defect | Specific Granule Deficiency | Schizotypal Personality Disorder | B-cell Chronic Lymphocytic Leukemia | Moyamoya Disease | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Spondylosis | Aspartylglycosaminuria | Tatton-Brown-Rahman Syndrome | Pancreatitis, Chronic | Membranous Nephropathy | Antley-Bixler Syndrome | Gyrate Atrophy Of The Choroid And Retina | Leukemia-lymphoma, Adult T-cell | Nephrotic Syndrome | Vestibular Disease | Achondrogenesis | Nephritis, Interstitial | Inflammatory Linear Verrucous Epidermal Nevus | Glycogen Storage Disease Type 1 | Mabry Syndrome | Epilepsy | Recurrent Respiratory Papillomatosis | Pyelonephritis | Carbonic Anhydrase VA Deficiency | Usher Syndrome Type IIC | Ellis-Van Creveld Syndrome | Diabetic Neuropathy | Familial Retinal Arterial Macroaneurysm | Maple Syrup Urine Disease | Congenital Tufting Enteropathy | Cockayne Syndrome | Lung Diseases | Guillain-Barre Syndrome | Cohen Syndrome | Ameloblastic Carcinoma | Charcot-Marie-Tooth Disease Type 4D | Keratitis-ichthyosis-deafness Syndrome | Asthma | Enlarged Vestibular Aqueduct | Hypercholesterolemia | Thyrotoxic Periodic Paralysis | Parkinson's Disease | Discoid Lupus Erythematosus | Spinocerebellar Ataxia Type 38 | Cerebral Amyloid Angiopathy | Nemaline Myopathy | Tonsillitis | Periventricular Leukomalacia | Colitis, Collagenous | Leiomyosarcoma | Hemophagocytic Lymphohistiocytosis | Hypokalemic Periodic Paralysis | Hereditary Sensory And Autonomic Neuropathy | Double Outlet Right Ventricle | Retinitis Pigmentosa 3 | Holoprosencephaly | Usher Syndrome Type I | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Epidermolysis Bullosa Dystrophica | Infantile Refsum Disease | Encephalocele | Mitochondrial Encephalomyopathy | Cheilitis | Pneumonia, Bacterial | Hyper IgE Syndrome | Hemolytic Uremic Syndrome | Chronic Mucocutaneous Candidiasis | Hypoparathyroidism | Mesothelioma, Malignant | Epidermolysis Bullosa | Schizophrenia | Lactose Intolerance | Dupuytren Disease | Pyruvate Decarboxylase Deficiency | KBG Syndrome | Pachyonychia Congenita | Geleophysic Dysplasia | Optic Neuropathy, Anterior Ischemic | Mandibuloacral Dysplasia With Type A Lipodystrophy | Polycystic Kidney, Autosomal Recessive | Renal Dysplasia | Pathological Gambling | Gnathodiaphyseal Dysplasia | Retinal Telangiectasia | Alpers Syndrome | Galactosemia | Proteasome-associated Autoinflammatory Syndrome 2 | Crohn's Disease | Infantile Liver Failure Syndrome 1 | Generalized Epilepsy And Paroxysmal Dyskinesia | Sepiapterin Reductase Deficiency | Retinoschisis | Posterior Polar Cataract | Adenoma, Pleomorphic | Spondyloepiphyseal Dysplasia Tarda, X-linked | Systemic Mastocytosis | Alpha-mannosidosis | Large Granular Lymphocytic Leukemia | Precocious Puberty | Hairy Cell Leukemia | Frank-ter Haar Syndrome | Diabetes | Xeroderma Pigmentosum | Adenomyosis | Cardiospondylocarpofacial Syndrome | Epidermolytic Hyperkeratosis | Syndactyly | Mannosidase Deficiency Diseases | Macrophage Activation Syndrome | Keratosis | Mucormycosis | Plasma Cell Dyscrasia | Endophthalmitis | Neuromuscular Disorders | Hereditary Coproporphyria | Papulopustular Rosacea | Lattice Corneal Dystrophy | Motion Sickness | Graft-versus-host Disease | Basal Ganglia Cerebrovascular Disease | Acute Chest Syndrome | Spondylolisthesis | Beta-Propeller Protein-associated Neurodegeneration | Neurofibromatosis Type 1 | Brachydactyly | Intellectual Disability, Autosomal Dominant 5 | Acne Vulgaris | Congenital Primary Aphakia | Ganglioneuroma | CDKL5 Deficiency Disorder | Metabolic Diseases | Anencephaly | C3 Glomerulonephritis | Birk-Barel Syndrome | Anorexia Nervosa | Hypersensitivity | Peripheral Neuropathy | Multiple System Atrophy | Alpha-thalassemia Myelodysplasia Syndrome | Early Infantile Epileptic Encephalopathy 1 | Transthyretin-related Amyloidosis | Hennekam Lymphangiectasia-lymphedema Syndrome | Diabetes Insipidus, Neurogenic | Endometritis | Arthrogryposis | Heimler Syndrome | Familial Glucocorticoid Deficiency | Amenorrhea | Hyperthermia, Malignant | Peyronie's Disease | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Patent Foramen Ovale | GAPO Syndrome | Chronic Lymphocytic Leukemia | Ornithine Transcarbamylase Deficiency | Vitreoretinopathy, Proliferative | Filariasis | Sickle Cell Disease | Persistent Mullerian Duct Syndrome | Progressive Familial Intrahepatic Cholestasis Type 1 | Glycogen Storage Disease Type 9 | Cholestasis | Cousin Syndrome | Anxiety Disorders | Seminoma | Sandhoff Disease | GATA2 Deficiency | Cerebellar Ataxia, Cayman Type | Herpes Genitalis | Glaucoma | Osteopathia Striata With Cranial Sclerosis | Spondylometaphyseal Dysplasia | Trichotillomania | Lassa Fever | Chordoid Glioma | Pierson Syndrome | Hypoproteinemia, Hypercatabolic | Familial Pheochromocytoma-paraganglioma | Spastic Paraplegia Type 7 | Zollinger-Ellison Syndrome | Waardenburg Syndrome | Anti-glomerular Basement Membrane Disease | Withdrawal Syndrome | Galactosialidosis | Diffuse Mesangial Sclerosis | Tumoral Calcinosis | Inflammatory Bowel Disease | Renal Medullary Carcinoma | Sporadic Hemiplegic Migraine | Poirier-Bienvenu Neurodevelopmental Syndrome | Microcephaly | Bronchiectasis | Cervical Dystonia | Pseudoexfoliation Syndrome | Olmsted Syndrome | Retinal Diseases | Pre-eclampsia | Sengers Syndrome | Spina Bifida | Spinocerebellar Ataxia Type 16 | Glomerulonephritis, Membranoproliferative | Polymyalgia Rheumatica | Hypogammaglobulinemia | Colorectal Adenoma | ACTH-independent Macronodular Adrenal Hyperplasia | Evans Syndrome | 3C Syndrome | Muir-Torre Syndrome | Neutrophilia | IgA Deficiency | Acute Coronary Syndrome | Lymphoma, AIDS-related | Stargardt Disease | Hashimoto Thyroiditis | Hypertension, Pulmonary | Neuromyelitis Optica | Blomstrand Osteochondrodysplasia | Pupil Disorders | Porphyria, Acute Intermittent | Bare Lymphocyte Syndrome | Greig Cephalopolysyndactyly Syndrome | FG Syndrome | Hereditary Pyropoikilocytosis | Congenital Lipoid Adrenal Hyperplasia | Epiphyseal Chondrodysplasia, Miura Type | Limb Girdle Muscular Dystrophy | Spinal Cord Diseases | Benign Familial Neonatal Convulsions | Endocarditis | Diabetes Gestational | Carney Triad | Arthritis | Chronic Inflammatory Demyelinating Polyneuropathy | Lymphedema | Incontinentia Pigmenti | Nager Acrofacial Dysostosis | Subcortical Band Heterotopia | Spinocerebellar Ataxia Type 27 | Hyperferritinemia-cataract Syndrome | Familial Isolated Hyperparathyroidism | Pancreatitis | Sclerosing Cholangitis | Iron Overload | Cutaneous Mastocytosis | Acquired Partial Lipodystrophy | T-cell Chronic Lymphocytic Leukemia | Schwartz-Jampel-Aberfeld Syndrome | Constipation | Carey-Fineman-Ziter Syndrome | Epilepsy Of Infancy With Migrating Focal Seizures | Angina Pectoris | Myocarditis | Small Lymphocytic Lymphoma | X-linked Myotubular Myopathy | Hepatitis | ICF Syndrome | Congenital Poikiloderma | Osteoporosis-pseudoglioma Syndrome | Erythema Nodosum | Melanoma, Malignant | Cancer, Colon | Waardenburg Syndrome Type 2 | Coffin-Lowry Syndrome | Cat Eye Syndrome | Pantothenate Kinase-associated Neurodegeneration | Adenoma, Villous | Leukocyte Adhesion Deficiency | CEDNIK Syndrome | Arteriosclerosis | Growth Hormone Excess | Majeed Syndrome | Hemangioblastoma | Purpura | Benign Familial Pemphigus | Neovascular Glaucoma | Cone Dystrophy | T-cell Prolymphocytic Leukemia | Myelomeningocele | Ichthyosis, X-linked | Fuchs Dystrophy | Urolithiasis | Aldosterone Deficiency | Preaxial Polydactyly | Kernicterus | Encephalitis, Tick-borne | Rolandic Epilepsy | Neurofibromatosis-Noonan Syndrome | Uveitis, Anterior | Gitelman Syndrome | Meniere's Disease | Carcinoid Tumor | Pneumothorax | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Hypercalciuria | Scapuloperoneal Spinal Muscular Atrophy | Pneumococcal Meningitis | Charcot-Marie-Tooth Disease, Type 1A | Juvenile Myelomonocytic Leukemia | Vogt-Koyanagi-Harada Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Lymphedema-distichiasis Syndrome | Sclerosteosis 2 | Addison Disease | Strabismus | Kashin-Beck Disease | Glutathione Synthetase Deficiency | Colitis | Leukodystrophies | Alkaptonuria | Contact Dermatitis | Neuroectodermal Tumors, Primitive | Angelman Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Schwannoma | Tenosynovial Giant Cell Tumor | Pyloric Stenosis, Infantile Hypertrophic | Neurofibrosarcoma | Congenital Ichthyosiform Erythroderma | Pseudohypoparathyroidism Type 1C | Malignant Fibrous Histiocytoma | Lymphoma Lymphoblastic | Achromatopsia | Saul-Wilson Syndrome