Disease

Bardet-Biedl Syndrome

About the Disease
Bardet-Biedl Syndrome, also known as bbs, is related to bardet-biedl syndrome 11 and bardet-biedl syndrome 1. An important gene associated with Bardet-Biedl Syndrome is BBS1 (Bardet-Biedl Syndrome 1), and among its related pathways/superpathways are Organelle biogenesis and maintenance and Ciliary landscape. The drugs Pharmaceutical Solutions and Hormones have been mentioned in the context of this disorder. Affiliated tissues include eye, kidney and retina, and related phenotypes are intellectual disability and abnormal electroretinogram

Common Targets
TTC21B | FBN3 | CORO2B | CFAP418 | G3630 | NPHP4 | BBS2 | IFT74 | TMEM67 | TMEM216 | BBS12 | PDE5A | MKS1 | IFT27 | MC3R | CEP290 | BBS7 | BBS5 | CCDC28B | ALMS1 | CEP19 | GJA1 | MC4R | ARL6 | SCAPER | TTC8 | SDCCAG8 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | BBIP1 | AMP-activated protein kinase (AMPK) | WDPCP | LZTFL1 | BBS4 | MKKS | MC1R | BBS1 | GLI1 | BBS10 | NPHP1 | AHI1 | IFT172 | BBS9 | SLC3A1

疾病靶点研报
Bardet-Biedl Syndrome

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

Other Diseases

Charcot-Marie-Tooth Disease Type 4D | Fatty Aldehyde Dehydrogenase Deficiency | Vascular Calcification | Chromosome 5q Deletion Syndrome | Personality Disorders | Stuttering | Apraxia | Chordoma | Bulimia Nervosa | Beta-Propeller Protein-associated Neurodegeneration | Birk-Barel Syndrome | Trigonocephaly | Centronuclear Myopathy | Nutrition Disorders | Nanophthalmos | CHARGE Syndrome | Schwannoma | Fuchs Heterochromic Iridocyclitis | Familial Pheochromocytoma-paraganglioma | Gardner Syndrome | Congestive Heart Failure | Supravalvular Aortic Stenosis | Alpha-thalassemia Myelodysplasia Syndrome | Diabetes Insipidus | Fontaine Progeroid Syndrome | Macular Corneal Dystrophy Type 1 | Pulmonary Tuberculosis | Cysticercosis | Proopiomelanocortin Deficiency | Charcot-Marie-Tooth Disease Type 2D | Osteogenesis Imperfecta Type V | Arthritis, Psoriatic | Palsy, Cerebral | Prune Belly Syndrome | Intestinal Tuberculosis | Pfeiffer Syndrome | Hemorrhagic Disorders | Shprintzen-Goldberg Syndrome | NDH Syndrome | Stroke | Loeys-Dietz Syndrome | Ornithine Transcarbamylase Deficiency | Juvenile Xanthogranuloma | Paternal Uniparental Disomy Of Chromosome 14 | Sclerocornea | Myocarditis | Idiopathic Multicentric Castleman Disease | Alveolar Capillary Dysplasia | Schwartz-Jampel-Aberfeld Syndrome | Lymphoma, B-cell | Diabetes | Trachoma | Neuroleptic Malignant Syndrome | Chronic Neutrophilic Leukemia | Poirier-Bienvenu Neurodevelopmental Syndrome | Tatton-Brown-Rahman Syndrome | Rhabdoid Tumor | Von Willebrand Disease | Sarcoidosis, Pulmonary | Optic Nerve Hypoplasia, Bilateral | Hepatitis, Chronic | Camurati-Engelmann Disease | Nemaline Myopathy 10 | Pilomatrix Carcinoma | Malignant Fibrous Histiocytoma | Spinal Muscular Atrophy Type 3 | Gigantism | Sarcomatoid Carcinoma Of The Lung | Ocular Albinism Type 1 | Combined Deficiency Of Factor V And Factor VIII | Renal Tubular Dysgenesis | Giant Axonal Neuropathy | Insulin Resistance | Metatropic Dysplasia | Ichthyosis, X-linked | Charcot-Marie-Tooth Disease, Type 6 | Hepatorenal Syndrome | Hyperthermia, Malignant | Familial Mediterranean Fever | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Adenoid Cystic Carcinoma | Reflex Epilepsy | Potocki-Shaffer Syndrome | Strabismus | Hodgkin Lymphoma | Cystinuria | Subacute Sclerosing Panencephalitis | Early Infantile Epileptic Encephalopathy 13 | Progressive Familial Intrahepatic Cholestasis | Cryptosporidiosis | Parvovirus B19 Infection | Epithelioid Hemangioma | Persistent Fetal Circulation | Measles | Hypohidrotic Ectodermal Dysplasia | Nephrocalcinosis | Danon Disease | Lymphedema | Hypersensitivity Pneumonitis | Vitreoretinopathy, Proliferative | Walker-Warburg Syndrome | Apparent Mineralocorticoid Excess Syndrome | Blastoma, Pleuropulmonary | Craniometaphyseal Dysplasia | Mumps | Sporadic Inclusion Body Myositis | Congenital Hereditary Endothelial Dystrophy Type II | Leigh Syndrome | Subcortical Band Heterotopia | Pulmonary Vein Stenosis | Thrombophilia | Crohn's Disease | VACTERL/VATER Association | Cholangitis | Pemphigus | Neurofibromatosis Type 1 | Schizotypal Personality Disorder | Proteus Syndrome | Nicotine Dependence | Leiomyoma | Acrodermatitis Enteropathica | Muscular Dystrophy | Coronary Heart Disease | Stickler Syndrome | Distal Myopathy | Shwachman-Bodian-Diamond Syndrome | High Molecular Weight Kininogen Deficiency | Ocular Hypertension | Sleep Apnea, Obstructive | Thanatophoric Dysplasia | Glycogen Storage Disease | Varicocele | Phenylketonuria II | McCune-Albright Syndrome | Dengue Shock Syndrome | Giant Cell Glioblastoma | Congenital Nephrotic Syndrome | Charcot-Marie-Tooth Disease Type 3 | Acral Lentiginous Melanoma | Asphyxia Neonatorum | Cholestasis, Intrahepatic | Pain | Optic Neuropathy | CEDNIK Syndrome | Optic Neuritis | Anuria | Coenzyme Q10 Deficiency | Schizencephaly | Dermatitis | Saul-Wilson Syndrome | X-linked Myotubular Myopathy | Acne | Trichothiodystrophy | Alstrom Syndrome | Progressive Familial Intrahepatic Cholestasis Type 1 | Bone Marrow Necrosis | Combined Malonic And Methylmalonic Acidemia | Asthma, Exercise-induced | NGLY1 Deficiency | Platelet Disorders | Iron Deficiency Anemia | Seasonal Mood Disorder | Osteoarthritis | Chronic Thromboembolic Pulmonary Hypertension | Psoriasis | Charcot-Marie-Tooth Disease Axonal Type 2N | Hereditary Mixed Polyposis Syndrome | Congenital Nystagmus | Acrodermatitis | Macular Corneal Dystrophy | Multifocal Motor Neuropathy | Granuloma Annulare | Mucolipidosis | Spinocerebellar Ataxia | Hepatitis E | Endometriosis | Multiple Sclerosis | Glycogen Storage Disease Type 5 | Hypertensive Nephropathy | Keratitis | Protein S Deficiency | Disseminated Intravascular Coagulation | Perivascular Epithelioid Cell Tumor | Thrombocytopenia | Genitopatellar Syndrome | Erythematotelangiectatic Rosacea | Hydronephrosis | Nail-Patella Syndrome | Intestinal Obstruction | Hypermethioninemia | Mevalonate Kinase Deficiency | Heterotopic Ossification | Nephropathy | Vulvovaginitis | Progressive Familial Intrahepatic Cholestasis Type 3 | Mastitis | Cardiomyopathy, Hypertrophic | Glycogen Storage Disease Type 9 | Temporal Lobe Epilepsy | Hashimoto Thyroiditis | Carcinoma, Squamous Cell | Argininosuccinic Aciduria | Hypoparathyroidism | Headache | Porphyria, Variegate | Progressive Myoclonic Epilepsy | Glomerulonephritis, Membranoproliferative | 3-M Syndrome | Narcolepsy | Chorea-acanthocytosis | Cancer, Skin | Bursitis | Papillon-Lefevre Syndrome | Schistosomiasis Mansoni | Opisthorchiasis | Avellino Corneal Dystrophy | MELAS Syndrome | Kindler Syndrome | Meningioma, Benign | Tibial Muscular Dystrophy | Hyperparathyroidism-jaw Tumor Syndrome | Interstitial Lung Diseases | Cat Eye Syndrome | Glaucoma, Congenital | Papilloma | Systemic Lupus Erythematosus | Fowler's Syndrome | Basan Syndrome | Usher Syndrome Type III | Porencephaly | Disseminated Superficial Actinic Porokeratosis | Analgesia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Metachondromatosis | Greig Cephalopolysyndactyly Syndrome | Glioblastoma | Endophthalmitis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Congenital Diaphragmatic Hernia | Hyperammonemia | Lyme Disease | Stroke, Ischemic | Polycystic Kidney, Autosomal Recessive | Chronic Kidney Disease | Basal Ganglia Cerebrovascular Disease | Alzheimer Disease, Late Onset | Hyperacusis | Seborrheic Dermatitis | Sengers Syndrome | Epidermolytic Ichthyosis, Annular | Botulism | Evans Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Ganglioglioma | Peripheral Neuropathy | COACH Syndrome | Goldenhar Syndrome | Oculodentodigital Dysplasia | Snyder-Robinson Syndrome | Whipple's Disease | Osteogenesis Imperfecta Type I | Microvillus Inclusion Disease | Encephalopathy, Glycine | Dysferlinopathy | Alopecia | Hereditary Inclusion Body Myopathy | Hemolytic Anemia | Neurotoxicity | Polycystic Kidney, Autosomal Dominant | Spondylocarpotarsal Synostosis Syndrome | Cirrhosis | Retinoblastoma | Polyomavirus Nephropathy | Histiocytosis | Demyelinating Diseases | Impulse Control Disorder | Cramp Fasciculation Syndrome | Ehlers-Danlos Syndrome | Hypertension, Renovascular | Intermittent Explosive Disorder | Gastrointestinal Disorders | Irritable Bowel Syndrome | Acute Anterior Uveitis | Melanoma | Thyroiditis | Castleman Disease | Blepharoconjunctivitis | Liver Diseases | Lymphoma, Mantle Cell | Li-Fraumeni Syndrome | Pulmonary Alveolar Microlithiasis | Esthesioneuroblastoma | Cushing Syndrome | HANAC Syndrome | Acute Tubular Necrosis | Anterior Segment Dysgenesis | Dementia, Vascular | Cholecystitis | Hypercholesterolemia | Bruck Syndrome | Choroiditis | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Hyperuricemic Nephropathy, Familial Juvenile | Jaundice, Obstructive | Central Pain Syndrome | Hypoglycemia | Swine Influenza | Primary Hyperoxaluria Type 3 | Viral Meningitis | Seizures | Nager Acrofacial Dysostosis | Peripheral T-cell Lymphoma | Congenital Primary Aphakia | Primary Hyperoxaluria Type 1 | Infantile Liver Failure Syndrome 1 | LEOPARD Syndrome | Alopecia Totalis | Primary Torsion Dystonia | Huntington's Disease-like 2 | AIDS | Autonomic Nervous System Disorders | Anemia | Congenital Hypofibrinogenemia | Infantile Nephropathic Cystinosis | Schnyder Crystalline Corneal Dystrophy | Kidney Stones | Postpartum Depression | Pseudohypoaldosteronism | Fabry's Disease | Pitt-Hopkins Syndrome | Spinocerebellar Ataxia Type 8 | Rickets | Empyema | Spinocerebellar Ataxia Type 5 | Otosclerosis | Hereditary Folate Malabsorption | Hereditary Hemorrhagic Telangiectasia Type 2 | LRBA Deficiency | Neural Tube Defect | Charcot-Marie-Tooth Disease, Type 1A | Amenorrhea | Large Granular Lymphocytic Leukemia | Schuurs-Hoeijmakers Syndrome | Currarino Syndrome | Congenital Stationary Night Blindness | Familial Isolated Hyperparathyroidism | Melanocytic Nevus | Chorioretinitis | Osteogenesis Imperfecta Type IV | Waardenburg Syndrome | Autonomic Neuropathy | Ameloblastic Carcinoma | Uremic Pruritus | Anorectal Malformations | Non-small Cell Lung Cancer | 5-oxoprolinase Deficiency | Rhabdomyosarcoma, Embryonal | Urolithiasis | T-cell Leukemia | Angiosarcoma | Distal Spinal Muscular Atrophy | Neuromuscular Disorders | Heimler Syndrome | Chudley-McCullough Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Primrose Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Primary Aldosteronism | Ischemia | Dengue Hemorrhagic Fever | AIDS Dementia Complex | Arts Syndrome | Cenani-Lenz Syndactyly Syndrome | Leukocyte Adhesion Deficiency Type 1 | Sleep Disorder | Polycystic Liver | Dyskeratosis Congenita | Congenital Fiber-type Disproportion Myopathy | Papilledema | Vasculitis | Carcinoid Tumor | Creutzfeldt-Jakob Disease | Carey-Fineman-Ziter Syndrome | Hypospadias | Nicotine Addiction | Milk Allergy | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | VACTERL Association | Arthritis | Multiple Sclerosis, Secondary Progressive | Enhanced S-cone Syndrome | Mucolipidosis Type III | Pierpont Syndrome | Hyperthyroidism | Cerebral Cavernous Malformations | Calcium Pyrophosphate Deposition Disease | Diamond-Blackfan Anemia | Chronic Mucocutaneous Candidiasis | Follicular Dendritic Cell Sarcoma | Richter's Syndrome