Disease

Hypercholesterolemia

About the Disease
Hypercholesterolemia, Familial, 3, also known as hypercholesterolemia, autosomal dominant, 3, is related to hyperaldosteronism, familial, type iii and strabismus. An important gene associated with Hypercholesterolemia, Familial, 3 is PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9). The drugs Probucol and Cilostazol have been mentioned in the context of this disorder. Affiliated tissues include heart, endothelial and skin, and related phenotypes are hypercholesterolemia and xanthelasma

Common Targets
APOE | GLP1R | G5743 | Monoamine oxidase (MAO) (nonspecified subtype) | GCGR | SREBF1 | ASGR1 | Asialoglycoprotein Receptor (ASGPR) (nonspecified subtype) | NADPH Oxidase (nonspecified subtype) | CYP19A1 | APOA2 | CETP | SPP1 | LPL | G7422 | Prolyl 4-hydroxylase | HSD17B2 | FFAR4 | Proteasome Complex | CYP3A4 | G5243 | CCN1 | SNCA | RLN3 | TRIB1 | APOA4 | LDLR | CYP7A1 | PREP | APOA5 | KDR | FFAR1 | G3576 | G1956 | THRB | P4HA3 | NPC1L1 | SLCO2B1 | NR1H2 | FDFT1 | G7015 | ANGPTL3 | DGAT2 | HDAC2 | Chymotrypsin (nonspecified subtype) | AGT | G7124 | ADIPOQ | HDAC6 | AMP-activated protein kinase (AMPK) | G595 | G3620 | Phospholipase A2 (nonspecified subtype) | Cholesterol esterase (nonspecified subtype) | CYP17A1 | SLC15A1 | SCARB1 | HIF1A | SORT1 | NR1H3 | RPS6KB1 | Liver Bile Transporters (LBAT) (nonspecified subtype) | ELANE | GPR146 | ACE | MIR122 | LIPA | S1PR4 | LTA | PPARA | Calcium channel (nonspecified subtype) | IL1B | Lipoxygenase (nonspecified subtype) | LDLRAP1 | APOC3 | Oxysterols receptor LXR (nonspecified subtype) | Acetylcholine Receptors (Nicotinic) (nAChR) (nonspecified subtype) | Peroxisome Proliferator-Activated Receptors (PPAR) (nonspecified subtype) | ESR2 | PCSK9 | HMGCR | NPPA | G4780 | NPPA-AS1 | G4137 | GIPR | NR1I2 | ABCA1 | CELSR2 | S1PR3 | ABCG5 | Histone acetyltransferase (HAT) (nonspecified subtype) | NF-kappaB (NFkB) | DYRK1A | ABCC2 | NPY | Estrogen receptor (nonspecified subtype) | CES1 | HSD11B1 | P4HB | PPARD | SLC10A1 | DPP4 | Reverse transcriptase (Telomerase) | G7099 | MTTP | ATP7B | ABCG8 | P2RY12 | HDAC1 | AKR1B1 | Trypsin (nonspecified subtype) | Voltage-Gated Sodium Channel Complex | CASP8 | G3605 | ADORA3 | Triacylglycerol Lipase (TG Lipase) (nonspecified subtype) | SOAT1 | G6PC1 | LIPC | LSS | XDH | OSBP | GSK3B | APOC1 | PTGS1 | PTPN1 | G9429 | NR1H4 | ACHE | SQLE | PPARG | RXRA | CYP3A5 | HNF1A | G3480 | Sterol O-acyltransferase (ACAT) (nonspecified subtype) | FAAH | STK25 | Platelet-Derived Growth Factor Receptor (nonspecified subtype) | TXNRD1 | FGFR4 | ACACB | G2099 | G3630 | Sodium channel (nonspecified subtype) | HCAR3 | SLC10A2 | APOA1 | FASN | G836 | Poly [ADP-ribose] polymerase (nonspecified subtype) | Mitogen-Activated Protein Kinase (nonspecified subtype) | SLC5A1 | AP-1 Transcription Factor Complex | ACLY | FASLG | HSD17B1 | Sterol Regulatory Element-Binding Protein (nonspecified subtype) | SOAT2 | ADRB2 | MRAS | FMO3 | LIPE | G1786 | SLCO1B1 | LPA | ERP44 | PNLIP | HCAR2 | NOX3 | APOB | MBOAT4 | UGT1A1 | THRA | FSHB | P4HA2 | G367 | NADPH Oxidase Complex | SIK3 | GLA | ENOX2 | TRPM3 | LIPG | S1PR1

疾病靶点研报
Hypercholesterolemia

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

Other Diseases

Venous Insufficiency | Creatine Deficiency Syndrome Due To AGAT Deficiency | Glucagonoma | Speech Disorders | Thrombasthenia | Hereditary Pyropoikilocytosis | Omenn Syndrome | Gastritis, Atrophic | Salla Disease | Primary Torsion Dystonia | Acute Lung Injury | Goiter | Postpoliomyelitis Syndrome | Rotor Syndrome | Hepatitis, Autoimmune | Gitelman Syndrome | Primary Pigmented Nodular Adrenocortical Disease | Pulmonary Alveolar Proteinosis | Thrombosis | Stroke | Schizencephaly | Progressive Encephalopathy-optic Atrophy Syndrome | Anosmia, Congenital | Tendinopathy | Micropenis | Teratozoospermia | Juvenile Polyposis | Pseudohypoparathyroidism Type 1A | Primary Hyperoxaluria Type 3 | X-linked Myotubular Myopathy | Spinocerebellar Ataxia Type 2 | Sandhoff Disease | Bronchitis | Arterial Tortuosity Syndrome | Trismus-pseudocamptodactyly Syndrome | Chronic Periodontitis | Ganglioglioma | Impulse Control Disorder | Reye Syndrome | Melanoma, Malignant | Niemann-Pick Disease, Type C | Small Lymphocytic Lymphoma | Campomelic Dysplasia | Spermatocele | Hyperparathyroidism, Primary | Hennekam Lymphangiectasia-lymphedema Syndrome | Ichthyosis, X-linked | Alpha-mannosidosis | Methylmalonic Aciduria And Homocystinuria, CblC Type | Macular Corneal Dystrophy Type 1 | Lymphomatoid Granulomatosis | Focal Cortical Dysplasia Type 2 | Neuroleptic Malignant Syndrome | Thyroid Dyshormonogenesis | Early Infantile Epileptic Encephalopathy | Microcephaly | Hemangioendothelioma | Schistosomiasis | Epidermodysplasia Verruciformis | Giant Axonal Neuropathy | LMNA-related Congenital Muscular Dystrophy | Pseudohypoparathyroidism Type 1C | Autoimmune Polyendocrine Syndrome | Micro Syndrome | Progressive Familial Intrahepatic Cholestasis | Ovarian Hyperstimulation Syndrome | Usher Syndrome Type I | Cancer, Lung | Loeys-Dietz Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Pneumonia, Mycoplasma | Kohlschutter-Tonz Syndrome | Acrodermatitis Enteropathica | Congenital Aniridia | Congenital Bilateral Absence Of Vas Deferens | Bone Marrow Necrosis | Gerodermia Osteodysplastica | Neuroblastoma | Spasticity | Pregnancy, Ectopic | Hypoparathyroidism | Osteomyelitis | Fowler's Syndrome | Methemoglobinemia Type IV | Kindler Syndrome | Periventricular Leukomalacia | Hereditary Multiple Exostoses | Hyperhomocysteinemia | Common Cold | Hartsfield Syndrome | Congenital Adrenal Hyperplasia | Cancer, Breast | Iron Metabolism Disorders | Mucolipidosis Type III | Autism Spectrum Disorders | Carcinoma, Squamous Cell | Anal Fissure | Epidermolysis Bullosa Simplex, Localized | Immunoproliferative Disorders | Calcium Pyrophosphate Deposition Disease | Vasculitis | Nicotine Dependence | Neuropathy | Leukoplakia, Oral | Learning Disability | Hypospadias | Papilledema | Neuromuscular Disorders | Keratocystic Odontogenic Tumor | Dystonia-parkinsonism, X-linked | Intermittent Explosive Disorder | Endometriosis | Ectodermal Dysplasia | Waardenburg Syndrome Type 2E | Chordoma | Noonan Syndrome | Mitochondrial Myopathy | Amblyopia | Erythromelalgia | AIDS Dementia Complex | Pyruvate Kinase Deficiency | Carcinoid Syndrome | Apraxia | COACH Syndrome | Polymyalgia Rheumatica | Aspergillosis | Scapuloperoneal Spinal Muscular Atrophy | Inflammatory Bowel Disease | Methemoglobinemia | Erythema Multiforme | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Joubert Syndrome 2 | Delayed Sleep Phase Syndrome | Priapism | Oculopharyngeal Muscular Dystrophy | Thanatophoric Dysplasia | Pouchitis | Pulmonary Stenosis | Noonan Syndrome-like Disorder With Loose Anagen Hair | Myelomeningocele | Gestational Trophoblastic Disease | Craniosynostosis | Nasodigitoacoustic Syndrome | Epidermolysis Bullosa | Asthma | Congenital Heart Defects | Chorea-acanthocytosis | Bernard-Soulier Syndrome | Hereditary Xerocytosis | Infertility, Male | Anterior Segment Dysgenesis | Intracranial Hypertension | Diabetic Nephropathy | Rhabdomyosarcoma, Alveolar | Uremic Pruritus | Cryptococcal Meningitis | Cysticercosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Pleomorphic Xanthoastrocytoma | Erectile Dysfunction | Vitreoretinal Degeneration, Snowflake Type | Optic Atrophy 2 | Japanese Encephalitis | Von Hippel-Lindau Disease | Basal Ganglia Disease | Acromicric Dysplasia | Keratosis, Actinic | Neurofibromatosis Type 2 | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Lactose Intolerance | Mucolipidosis Type IV | Hepatic Veno-occlusive Disease | Coffin-Siris Syndrome | Hamartoma | Saethre-Chotzen Syndrome | Peripheral Neuropathy | Central Core Disease | Atrioventricular Septal Defect | Cystinuria | Cataract | Polydactyly | Ehlers-Danlos Syndrome | Personality Disorders | Exostoses | Carotid Artery Disease | Oligoasthenoteratozoospermia | Fetal Alcohol Syndrome | Hepatic Adenomatosis | Hypertensive Retinopathy | Idiopathic Pulmonary Fibrosis | Sick Sinus Syndrome | Gastric Atrophy | Leukoencephalopathy, Progressive Multifocal | Malignant Peripheral Nerve Sheath Tumor | Specific Granule Deficiency | Keratoacanthoma | Lennox-Gastaut Syndrome | Galactosialidosis | Scleritis | Meningeal Melanocytoma | Nephroblastoma | Cabezas Syndrome | Leprosy | Retinitis Pigmentosa | Glutaric Aciduria Type 3 | Autosomal Recessive Congenital Ichthyosis | Hypertension, Pulmonary | Autosomal Recessive Spastic Paraplegia Type 54 | Malignant Fibrous Histiocytoma | X-linked Charcot-Marie-Tooth Disease | Ventricular Septal Defect | Beare-Stevenson Syndrome | Epilepsy | Hypopituitarism | Postaxial Polydactyly | Gardner Syndrome | Oligodendroglioma | Menkes Disease | Charcot-Marie-Tooth Disease Type 4 | Familial Partial Lipodystrophy | Sturge-Weber Syndrome | Multiple Epiphyseal Dysplasia | Superficial Spreading Melanoma | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Meier-Gorlin Syndrome | Tendinitis | Angioedema | Neonatal Progeroid Syndrome | Eclampsia | Citrullinemia | Burn-McKeown Syndrome | Retinal Coloboma | Chylothorax, Congenital | Diffuse Palmoplantar Keratoderma | Glioblastoma Multiforme | Uveitis, Anterior | Dent Disease | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Ophthalmia, Sympathetic | Neurofibrosarcoma | Lipid Storage Diseases | Paroxysmal Kinesigenic Dyskinesia | Spinocerebellar Ataxia Type 13 | Protein C Deficiency | Primary Carnitine Deficiency | Osteochondrosis | Melanoma, Uveal | Coma | Granuloma Annulare | Keratosis | Cancer, Prostate | Bronchiolitis | Spinal Muscular Atrophy Type 3 | Mitochondrial Cytopathy | Dentinogenesis Imperfecta | Pleural Tuberculosis | Schuurs-Hoeijmakers Syndrome | Marshall-Smith Syndrome | Endometritis | Hyperinsulinemic Hypoglycemia | Rett Syndrome | Stiff-man Syndrome | Panic Disorder | Idiopathic Multicentric Castleman Disease | Dysfibrinogenemia | Juvenile Xanthogranuloma | Creutzfeldt-Jakob Disease | Coronary Artery Disease | Congenital Myopathy | Pineoblastoma | Urofacial Syndrome | Cousin Syndrome | Spondylolisthesis | Kabuki Syndrome | Richter's Syndrome | Cone Dystrophy | Central Pain Syndrome | Cole-Carpenter Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Familial Advanced Sleep Phase Syndrome | Mitochondrial DNA Depletion Syndrome | Cystitis, Interstitial | Stargardt Disease | Fuchs Dystrophy | Allergic Contact Dermatitis | Pierre Robin Syndrome | Eccrine Porocarcinoma | Lattice Corneal Dystrophy | Myofibrillar Myopathy | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Glaucoma, Congenital | Dengue Hemorrhagic Fever | Myeloid Leukemia | Pneumonia, Viral | Charcot-Marie-Tooth Disease, Type 6 | Urea Cycle Disorder | Hemorrhoids | Hypotrichosis Simplex | Tricho-hepato-enteric Syndrome | Goiter, Nodular | Melnick-Needles Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Connective Tissue Disorders | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hypocalcemia | Hypothalamic Obesity | Temporal Lobe Epilepsy | Sickle Cell Disease | Retinal Dystrophy, Early-onset Severe | Turner's Syndrome | Intestinal Tuberculosis | Glycogen Storage Disease Type 1a | Bare Lymphocyte Syndrome | Infantile Spasm | Scabies | Kleine-Levin Syndrome | Mannosidase Deficiency Diseases | Cenani-Lenz Syndactyly Syndrome | Pearson Syndrome | Mycosis Fungoides | Amelogenesis Imperfecta | Silver-Russell Syndrome | Craniofrontonasal Syndrome | Lymphoma, B-cell | Fibromyalgia | Wolcott-Rallison Syndrome | Papilloma | Chronic Idiopathic Myelofibrosis | Neuromyotonia | Myocarditis | Osteosarcoma | Combined Malonic And Methylmalonic Acidemia | VEXAS Syndrome | Schistosomiasis Mansoni | Carbohydrate Metabolism Disorders | Syphilis | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Pulmonary Capillary Hemangiomatosis | Erythropoietic Protoporphyria | Hepatitis, Chronic | Sporadic Inclusion Body Myositis | Charcot-Marie-Tooth Disease Type 2E | Neurofibroma, Plexiform | Restrictive Dermopathy | Infantile Neuroaxonal Dystrophy | Zygomycosis | Nail-Patella Syndrome | Tetraplegia | Synpolydactyly | Spinal Cord Diseases | Crohn's Disease | Synovitis | Transcobalamin Deficiency | Trigonocephaly | Charcot-Marie-Tooth Disease, Type 2 | Demyelinating Diseases | Autosomal Recessive Bestrophinopathy | Varices | Muscle Wasting | Osteogenesis Imperfecta Type III | Nephritis, Interstitial | Chromosome 16p11.2 Deletion Syndrome | Astrocytoma | Hypoalbuminemia | Eosinophilia | Pericarditis | Otitis Media | Thrombophilia | Johanson-Blizzard Syndrome | Blepharoconjunctivitis | Encephalopathy | Woodhouse-Sakati Syndrome | Megalencephaly | Intellectual Disability, Autosomal Dominant 5 | Acute Coronary Syndrome | Chanarin-Dorfman Syndrome | Premature Ejaculation | Schizoaffective Disorder | Spinal And Bulbar Muscular Atrophy | Thyroid Hormone Resistance | Lafora Disease | Myhre Syndrome | Metachondromatosis | Photosensitivity | Lateral Meningocele Syndrome | Retinitis Pigmentosa 3 | CHOPS Syndrome | Corticobasal Syndrome | Extramammary Paget's Disease | Larsen Syndrome | Waardenburg Syndrome | Myasthenia Gravis | Cushing Syndrome | Peters-plus Syndrome | Charcot-Marie-Tooth Disease Type 4B1 | Lipid Metabolism Disorders | Vestibular Disease | Cutaneous Angiosarcoma | Focal Segmental Glomerulosclerosis | Blau Syndrome