Disease

Low Phospholipid Associated Cholelithiasis

About the Disease
Gallbladder Disease 1, also known as gallstones, is related to gallbladder disease and ovalocytosis, southeast asian. An important gene associated with Gallbladder Disease 1 is ABCB4 (ATP Binding Cassette Subfamily B Member 4). The drugs Ketamine and Dopamine have been mentioned in the context of this disorder. Affiliated tissues include liver, small intestine and kidney, and related phenotypes are intrahepatic cholestasis and abdominal colic

Common Targets
CDK2 | CDK5/p25 | ABCB4 | Casein kinase I (nonspecified subtype) | CDK5 | CDK9/Cyclin T1 | CDK9 | DYRK1A | CCNT1 | GSK3B | CDK2/Cyclin A | CLK1 | Cyclin A (nonspecified subtype)

疾病靶点研报
Low Phospholipid Associated Cholelithiasis

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

Other Diseases

Chronic Mucocutaneous Candidiasis | Evans Syndrome | Localized Scleroderma | Nutrition Disorders | Takayasu's Arteritis | Chudley-McCullough Syndrome | Schizencephaly | Epidermolysis Bullosa | Multiple Sclerosis, Secondary Progressive | Thrombotic Microangiopathy | Hereditary Coproporphyria | Osteochondroma | Gynecomastia | Low Tension Glaucoma | Platelet Disorders | Goldenhar Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Zellweger Syndrome | Coronary Heart Disease | Microcephaly | Skin Fragility-woolly Hair Syndrome | Hypothyroidism | Dental Caries | Pachyonychia Congenita | Spermatocele | 3-hydroxy-3-methylglutaric Aciduria | Keloid | Nephrotic Syndrome Type 1 | Mucolipidosis Type IV | Neurocutaneous Melanocytosis | LEOPARD Syndrome | Diabetic Neuropathy | Fraser Syndrome | Myocardial Infarction | Proteasome-associated Autoinflammatory Syndrome 2 | VACTERL/VATER Association | Wolfram Syndrome 2 | Adenoma, Pleomorphic | Spondylolisthesis | Eosinophilic Asthma | Arts Syndrome | Urolithiasis | Stroke | Progressive Familial Intrahepatic Cholestasis Type 2 | Lymphomatoid Granulomatosis | Hepatitis | Liver Failure, Acute Infantile | Delayed Sleep Phase Syndrome | Shprintzen-Goldberg Syndrome | Androgenic Alopecia | Micro Syndrome | Malignant Fibrous Histiocytoma | Stromal Corneal Dystrophy | Pleural Tuberculosis | Gnathodiaphyseal Dysplasia | Neurofibromatosis-Noonan Syndrome | Acute Anterior Uveitis | Precocious Puberty | Exfoliative Dermatitis | Agammaglobulinemia | Osteoporosis | Phenylketonuria II | Acute Chest Syndrome | Overactive Bladder | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Triphalangeal Thumb-polysyndactyly Syndrome | Malonyl-CoA Decarboxylase Deficiency | Chromosome 17q21.31 Deletion Syndrome | Fibrosis | Vitelliform Macular Dystrophy | Diarrhea | Ganglioneuroma | Beare-Stevenson Syndrome | Waardenburg Syndrome Type 2E | Hemangioblastoma | Hypogammaglobulinemia | Agranulocytosis | Vascular Calcification | Intestinal Pseudo-obstruction | Pseudo-pseudohypoparathyroidism | Dentinogenesis Imperfecta | Schamberg Disease | Sarcomatoid Carcinoma Of The Lung | Esophagitis, Eosinophilic | Anorexia Nervosa | Periventricular Leukomalacia | VEXAS Syndrome | Pineoblastoma | Hermansky-Pudlak Syndrome | Cutaneous T-cell Lymphoma | Familial Episodic Pain Syndrome | Familial Hypertrophic Cardiomyopathy | Aplasia Cutis Congenita | Vitamin K Deficiency | Bronchitis, Chronic | Long QT Syndrome Type 3 | Avellino Corneal Dystrophy | Meningitis | Pseudoexfoliation Syndrome | Diabetes Type 2 | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Migraine | Familial Glucocorticoid Deficiency | Pulmonary Alveolar Microlithiasis | Acquired Partial Lipodystrophy | Diastrophic Dysplasia | Peeling Skin Syndrome, Acral Type | Larsen Syndrome | Hernia, Inguinal | Progressive Familial Intrahepatic Cholestasis | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Biotinidase Deficiency | COACH Syndrome | Lymphedema-distichiasis Syndrome | Ataxia-ocular Apraxia 2 | Pearson Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Osteomalacia | Leukemia | Pupil Disorders | Osmotic Demyelination Syndrome | Neovascular Glaucoma | Hyperthyroidism | Gastric Atrophy | Niemann-Pick Disease, Type B | Macular Corneal Dystrophy | Leukocyte Adhesion Deficiency | Tendinopathy | Combined Pituitary Hormone Deficiency | Dementia | Adenomatoid Tumor | Hyperphenylalaninemia | Neurodegeneration With Brain Iron Accumulation | Molybdenum Cofactor Deficiency | Generalized Epilepsy With Febrile Seizures Plus | Pyruvate Decarboxylase Deficiency | Astrocytoma, Anaplastic | Large Granular Lymphocytic Leukemia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Pompe Disease | Pseudohermaphroditism | Pyoderma Gangrenosum | Pseudoachondroplasia | Hyperprolactinemia | Trichotillomania | Robinow Syndrome | Polymyalgia Rheumatica | Transcobalamin Deficiency | Presbyopia | Infantile Nephropathic Cystinosis | Globozoospermia | Anal Fissure | Retinal Vasculitis | Congenital Lipoid Adrenal Hyperplasia | Cancer, Skin | Hemochromatosis Type 1 | Niemann-Pick Disease, Type C | Fragile X Syndrome | Lipodystrophy | Aplastic Anemia | Glycogen Storage Disease Type 5 | Dystonia | Erectile Dysfunction | Tietze Syndrome | Pontocerebellar Hypoplasia Type 2 | Desbuquois Syndrome | Retinal Dystrophy | Hemophilia | Polycystic Kidney, Autosomal Recessive | Schistosomiasis | Familial Thoracic Aortic Aneurysm | Achromatopsia | Gastritis | Sclerocornea | Osteosarcoma | Oculodentodigital Dysplasia | Esophageal Motility Disorders | Greenberg Dysplasia | Intellectual Disability, Autosomal Dominant 5 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | X-linked Acrogigantism | Neuromyotonia | Hashimoto Thyroiditis | Rett Syndrome | Amelogenesis Imperfecta | Carcinoid Tumor | Hypertrophy | Intracerebral Hemorrhage | Fuchs Dystrophy | Conjunctivitis | Waardenburg Syndrome Type 2 | Congenital Tufting Enteropathy | Cervicitis | Frank-ter Haar Syndrome | X-linked Charcot-Marie-Tooth Disease | Parkinsonism | H Syndrome | Thin Basement Membrane Disease | Porphyria Cutanea Tarda | Takotsubo Cardiomyopathy | Bronchiolitis | Hypokalemia | Dystonia-parkinsonism, X-linked | Myelodysplasia | Spondylometaphyseal Dysplasia | Conjunctivitis, Allergic | Cardiospondylocarpofacial Syndrome | Personality Disorders | Gigantism | Niemann-Pick Disease | Liebenberg Syndrome | Episodic Ataxia Type 1 | Common Variable Immunodeficiency | Carbamoyl Phosphate Synthetase I Deficiency | Graves Disease | Subcortical Band Heterotopia | Benign Hereditary Chorea | Plasma Cell Leukemia | Scleroderma, Diffuse | Multiple System Atrophy | Adenoma, Pituitary | Carcinoma, Signet Ring Cell | Acromegaly | Retinopathy Of Prematurity | Multiple Myeloma | Photosensitivity | Pneumoconiosis | Congenital Disorders Of Glycosylation Type II | Hypopigmentation | Renal Medullary Carcinoma | Hereditary Sensory And Autonomic Neuropathy | Open-angle Glaucoma | Lewy Body Dementia | Primary Biliary Cholangitis | Klinefelter Syndrome | Benign Recurrent Intrahepatic Cholestasis 1 | Familial Retinal Arterial Macroaneurysm | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Cholesteryl Ester Storage Disease | Pantothenate Kinase-associated Neurodegeneration | Polycythemia Vera | Gitelman Syndrome | Hemorrhage | Lymphoproliferative Disease, X-linked | CHOPS Syndrome | Pigment Dispersion Syndrome | Ehlers-Danlos Syndrome | Camurati-Engelmann Disease | Actinomycetoma | Muscle Wasting | Liver Diseases | Von Willebrand Disease | Iron Overload | Ligneous Conjunctivitis | Abetalipoproteinemia | Mohr-Tranebjaerg Syndrome | Spinocerebellar Ataxia Type 21 | Trimethylaminuria | Postpoliomyelitis Syndrome | Lissencephaly 2 | N-acetylglutamate Synthase Deficiency | Blomstrand Osteochondrodysplasia | Intracranial Hypertension | Ependymoma | Congenital Nystagmus | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Agnathia-Otocephaly Complex | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Tonsillitis | Supravalvular Aortic Stenosis | Anti-NMDA Receptor Encephalitis | Corneal Neovascularization | Rhabdoid Tumor | Bulimia Nervosa | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Congenital Heart Block | Sialidosis | Encephalopathy | Whipple's Disease | Hypertension, Renovascular | Phenylketonuria | Mitochondrial Encephalomyopathy | Carotid Artery Disease | Alzheimer Disease, Late Onset | Smith-Lemli-Opitz Syndrome | Cryopyrin-associated Periodic Syndromes | Cutaneous Mastocytosis | Cold Agglutinin Disease | Adrenal Insufficiency | Carcinoma In Situ | Kabuki Syndrome | Dubin-Johnson Syndrome | Eccrine Porocarcinoma | MIRAGE Syndrome | Dysferlinopathy | Congestive Heart Failure | Infantile Refsum Disease | Hyperparathyroidism, Primary | T-cell Prolymphocytic Leukemia | Ichthyosis Hystrix, Curth-Macklin Type | Hypervalinemia | Patent Foramen Ovale | Hypodontia | Cancer, Brain | Spondylocostal Dysostosis | Angioimmunoblastic T-cell Lymphoma | Neonatal Progeroid Syndrome | Malnutrition | Brenner Tumor | Schaaf-Yang Syndrome | Familial Mediterranean Fever | Bone Giant Cell Tumor | C3 Glomerulonephritis | Osteogenesis Imperfecta Type VI | Leiomyoma | Non-bullous Congenital Ichthyosiform Erythroderma | Progressive Osseous Heteroplasia | Thanatophoric Dysplasia | Erythematotelangiectatic Rosacea | Adenoid Cystic Carcinoma | Alpha-mannosidosis | Turner's Syndrome | Urticaria | Hypoplastic Left Heart Syndrome | Nephrotic Syndrome | Sleep Apnea, Obstructive | Adenylosuccinate Lyase Deficiency | GM2-gangliosidosis AB Variant | Adenosine Deaminase Deficiency | Waardenburg Syndrome Type 2A | Schuurs-Hoeijmakers Syndrome | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Dysfibrinogenemia | Epidermolytic Hyperkeratosis | Dowling-Degos Disease | Hyperinsulinemia | Coffin-Lowry Syndrome | Knobloch Syndrome | Adams-Oliver Syndrome | Arteriosclerosis | Subacute Sclerosing Panencephalitis | Hepatitis B, Chronic | Cabezas Syndrome | Otitis Externa | Uremic Pruritus | Keratosis, Seborrheic | Scapuloperoneal Myopathy, X-linked Dominant | Cataract | Eating Disorder | Craniometaphyseal Dysplasia | B-cell Chronic Lymphocytic Leukemia | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Monilethrix | Spinocerebellar Ataxia Type 38 | Thrombocytopenia | Scapuloperoneal Spinal Muscular Atrophy | Lassa Fever | Hereditary Spherocytosis | Acute Kidney Injury | Beta-Propeller Protein-associated Neurodegeneration | Spondylo-ocular Syndrome | Multiple Sclerosis, Chronic Progressive | Panniculitis | Dwarfism | Central Core Disease | Fibrodysplasia Ossificans Progressiva | Joubert Syndrome 2 | Autonomic Nervous System Disorders | Loeys-Dietz Syndrome | Acrocallosal Syndrome | ICF Syndrome | ADNP Syndrome | Spastic Paraplegia Type 7 | HIBCH Deficiency | Crisponi Syndrome | Epidermolysis Bullosa Simplex, Generalized | Heart Septal Defects | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Lupus Erythematosus | Paraplegia | Hepatic Adenomatosis | Acrodermatitis Enteropathica | Patent Ductus Arteriosus | Acute Leukemia | Aceruloplasminemia | Autism | Isovaleric Acidemia | Atopic Dermatitis | Spitzoid Melanoma | Ectrodactyly | Becker Muscular Dystrophy | Cyst | Splenomegaly | Xeroderma Pigmentosum | Teratozoospermia | Plasmacytoma | Systemic Lupus Erythematosus | Familial Dysautonomia | Conduct Disorder | Erythromelalgia