Disease

Poirier-Bienvenu Neurodevelopmental Syndrome

About the Disease
Poirier-Bienvenu Neurodevelopmental Syndrome, also known as pobinds, is related to alacrima, achalasia, and mental retardation syndrome and cerebellar atrophy, developmental delay, and seizures. An important gene associated with Poirier-Bienvenu Neurodevelopmental Syndrome is CSNK2B (Casein Kinase 2 Beta). Affiliated tissues include tongue, and related phenotypes are intellectual disability and mandibular prognathia

Common Targets
FKRP | CSNK2B

疾病靶点研报
Poirier-Bienvenu Neurodevelopmental Syndrome

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

Other Diseases

Nephrotic Syndrome | Porphyria, Variegate | Non-Hodgkin Lymphoma | Synovitis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Congenital Hereditary Endothelial Dystrophy Type II | Primary Progressive Aphasia | Mast Cell Leukemia | Erdheim-Chester Disease | Gastroenteritis | Pulverulent Zonular Cataract | Chordoid Glioma | Colitis, Microscopic | Pycnodysostosis | Epithelioid Hemangioma | Farber Disease | Cardiomyopathy, Dilated, 1L | Neurofibroma, Plexiform | Monilethrix | Epidermal Nevus Syndrome | Infantile Neuroaxonal Dystrophy | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | AIDS | Osteosarcoma | SAPHO Syndrome | Charcot-Marie-Tooth Disease, Type 6 | Specific Granule Deficiency | Polyarteritis Nodosa | Emery-Dreifuss Muscular Dystrophy | Tracheal Disorders | Actinomycetoma | Lymphoma, AIDS-related | Osteogenesis Imperfecta Type III | Exotropia | Cholangitis | Pulmonary Alveolar Microlithiasis | Li-Fraumeni Syndrome | Nance-Horan Syndrome | Norrie Disease | Infectious Diarrhea | Smoldering Myeloma | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Congenital Hemolytic Anemia | Intestinal Obstruction | Leukemia-lymphoma, Adult T-cell | Cannabis Abuse | Hypersensitivity Pneumonitis | Paternal Uniparental Disomy Of Chromosome 14 | Anxiety Disorders | Reye Syndrome | Waldenstrom Macroglobulinemia | Episodic Ataxia Type 2 | Sorsby Fundus Dystrophy | Hypotension, Orthostatic | Prolactinoma | Ataxia-ocular Apraxia 2 | Pneumothorax | Cluster Headache | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Impulse Control Disorder | Macrophage Activation Syndrome | Corneal Dystrophy | Budd-Chiari Syndrome | Craniolenticulosutural Dysplasia | Alazami Syndrome | Schistosomiasis | Tyrosinemia Type 2 | Glutathione Synthetase Deficiency | Menkes Disease | Hypercholesterolemia | Pierson Syndrome | Scapuloperoneal Spinal Muscular Atrophy | FG Syndrome | Lymphoma, Mantle Cell | Spinocerebellar Ataxia Type 20 | Sarcoma, Alveolar Soft Part | Fucosidosis | Hemophilia | Hypopituitarism | Tonsillitis | Cardiomyopathy, Peripartum | Charcot-Marie-Tooth Disease Type 4 | Schwannoma | Lattice Corneal Dystrophy | Chitayat Syndrome | Macular Degeneration | Fibrillation, Atrial | Spinocerebellar Ataxia Type 7 | Coronary Heart Disease | Schuurs-Hoeijmakers Syndrome | Best Macular Dystrophy | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Pemphigus Vulgaris | Cerebellar Ataxia, Cayman Type | Neutrophilia | Dysmorphophobia | Protein C Deficiency | Craniosynostosis | Melnick-Needles Syndrome | Lipid Storage Myopathy | Thrombocytopenia | Sialidosis Type I | Dementia | GM2-gangliosidosis AB Variant | Glycogen Storage Disease Type 3 | Panniculitis | Krabbe Disease | Neurodevelopmental Disorders | Holt-Oram Syndrome | Wiedemann-Steiner Syndrome | Cramp Fasciculation Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Myoclonic Epilepsy With Ragged Red Fibers | Oligoasthenoteratozoospermia | Keratosis, Seborrheic | Alpha-1 Antitrypsin Deficiency | Asplenia | Hypohidrotic Ectodermal Dysplasia | Familial Digital Arthropathy-brachydactyly | Paroxysmal Kinesigenic Dyskinesia | Leukoencephalopathy, Progressive Multifocal | Pneumonia, Bacterial | Congenital Hereditary Endothelial Dystrophy Type I | Chloridorrhea, Congenital | Erythropoietic Protoporphyria | Hyperlipidemia | Gastrointestinal Disorders | Hepatoblastoma | Basal Cell Nevus Syndrome | Pulmonary Capillary Hemangiomatosis | Mucolipidosis Type IV | Cheilitis | Hyperthyroidism | Sensory Neuropathy | Carcinoma, Squamous Cell | Congenital Stationary Night Blindness | Congenital Nystagmus | Hereditary Spherocytosis | Tetraplegia | Nephroblastoma | Tendinitis | Combined Deficiency Of Factor V And Factor VIII | Desbuquois Syndrome | Osteogenesis Imperfecta Type II | Congenital Disorders Of Glycosylation | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Dupuytren Disease | Homocystinuria | Encephalitis | Adenocarcinoma | Hypothalamic Obesity | Bethlem Myopathy | Pseudo-pseudohypoparathyroidism | Lymphoma | Palsy, Cerebral | Zollinger-Ellison Syndrome | Camurati-Engelmann Disease | Glaucoma, Congenital | Duane Retraction Syndrome | Peripheral T-cell Lymphoma | Myositis | Galactosemia | Primary Ovarian Insufficiency | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Spinocerebellar Ataxia Type 31 | Rhizomelic Chondrodysplasia Punctata | McLeod Syndrome | Juvenile Hyaline Fibromatosis | Pantothenate Kinase-associated Neurodegeneration | Botulism | Mycosis Fungoides | Carbamoyl Phosphate Synthetase I Deficiency | Common Cold | Veno-occlusive Disease | Fetal Akinesia Deformation Sequence | Potocki-Shaffer Syndrome | Pompe Disease | Aplastic Anemia | Sjogren Syndrome | Viral Meningitis | Fibromuscular Dysplasia | Smith-Magenis Syndrome | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Silver-Russell Syndrome | Pupil Disorders | Macular Corneal Dystrophy Type 1 | Polycystic Kidney, Autosomal Dominant | Hypogammaglobulinemia | Aarskog-Scott Syndrome | Congenital Myopathy | Familial Mediterranean Fever | Arthropathy | Peritonitis | Thyroid Dysgenesis | Spondylo-ocular Syndrome | Cryopyrin-associated Periodic Syndromes | Dyskeratosis Congenita | Gastritis, Atrophic | Congenital Ichthyosiform Erythroderma | Polyomavirus Nephropathy | Dyslipidemia | Ependymoma | Ghosal Syndrome | Spinocerebellar Ataxia Type 28 | Diverticulitis | Arthritis, Reactive | Placenta Previa | Geleophysic Dysplasia | T-cell Leukemia | Non-proliferative Diabetic Retinopathy | Premature Ejaculation | Renal Tubular Dysgenesis | Nasodigitoacoustic Syndrome | Adrenomyeloneuropathy | Leber Congenital Amaurosis | Oculocutaneous Albinism Type 1 | Cardiofaciocutaneous Syndrome | Sepiapterin Reductase Deficiency | Asthma | Opisthorchiasis | Congenital Mirror Movements | Thalassemia, Beta | X-linked Sideroblastic Anemia | Seizures | Blomstrand Osteochondrodysplasia | Basal Ganglia Disease, Biotin-responsive | Heimler Syndrome | Spasticity | Melanoma | Dysgerminoma | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Diabetes Type 2 | Lathosterolosis | Retinal Detachment | Porphyria, Acute Intermittent | Proteasome-associated Autoinflammatory Syndrome 2 | Hepatitis, Autoimmune | Central Retinal Artery Occlusion | Fabry's Disease | Spinocerebellar Ataxia Type 38 | Carcinoma, Small Cell | Argininosuccinic Aciduria | Gilbert Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Prolymphocytic Leukemia | Membranous Nephropathy | Maple Syrup Urine Disease | Thyroiditis | Chiari Malformation Type I | Globozoospermia | Phenylketonuria | Amyotrophic Lateral Sclerosis | Neurodegeneration With Brain Iron Accumulation | Hemoglobinopathies | Hereditary Inclusion Body Myopathy | Hyperammonemia | Myeloid Leukemia | Autosomal Recessive Spastic Paraplegia Type 54 | Hidradenitis Suppurativa | Blastoma, Pleuropulmonary | Usher Syndrome Type IIC | Otitis Externa | Tylosis With Esophageal Cancer | Postpartum Depression | Cabezas Syndrome | Perry Syndrome | Graft-versus-host Disease | Myelodysplasia | Paraganglioma, Carotid Body | Marshall-Smith Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Anosmia, Congenital | Facioscapulohumeral Muscular Dystrophy Type 1 | Chromosome 9q34.3 Deletion Syndrome | Pelvic Inflammatory Disease | Ligneous Conjunctivitis | Myofibromatosis | Neovascular Glaucoma | Meesmann Corneal Dystrophy | Hypophosphatasia | Hemochromatosis | Adenomyosis | Ophthalmoplegia | Ectodermal Dysplasia | Adenoid Cystic Carcinoma | Sclerosing Cholangitis | Arthritis, Gouty | Aldosterone Deficiency | Zimmermann-Laband Syndrome | Anal Fissure | Intracranial Hypertension | Hepatitis, Alcoholic | Heroin Dependence | Brachydactyly | C3 Glomerulonephritis | Aspergillosis | Renal Failure | Impetigo | Retinopathy Of Prematurity | Perivascular Epithelioid Cell Tumor | Congenital Diaphragmatic Hernia | Liver Failure | Leiomyosarcoma | Goiter, Nodular | Cirrhosis | Keratosis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Cryptococcal Meningitis | Kaposiform Hemangioendothelioma | Thrombotic Microangiopathy | Pierpont Syndrome | Hypoglycemia | Aplasia Cutis Congenita | Diabetes Type 1 | Thrombocythemia, Essential | Craniofacial Dysostosis | Raine Syndrome | Cri-du-chat Syndrome | Pitt-Hopkins Syndrome | Low Phospholipid Associated Cholelithiasis | HELLP Syndrome | Hypertriglyceridemia | Hypogonadism | Congenital Fiber-type Disproportion Myopathy | Megaloblastic Anemia | Pyruvate Carboxylase Deficiency Disease | Congenital Heart Defects | Acute Coronary Syndrome | Anencephaly | Cystinuria | Okihiro Syndrome | Gangliosidosis, GM1 | Ichthyosis, X-linked | Multicentric Carpotarsal Osteolysis Syndrome | Knobloch Syndrome | Genitopatellar Syndrome | Liebenberg Syndrome | Antenatal Bartter Syndrome Type 1 | Hennekam Lymphangiectasia-lymphedema Syndrome | Miyoshi Myopathy | Dementia, Vascular | Kleine-Levin Syndrome | Heart Block | Eosinophilia | Hereditary Folate Malabsorption | Fahr Disease | Tremor | Esophagitis, Eosinophilic | Scoliosis | Benign Familial Pemphigus | Lung Diseases | Pendred Syndrome | Ischemia | Esophagitis | Pancytopenia | Lennox-Gastaut Syndrome | Japanese Encephalitis | Currarino Syndrome | Alopecia Totalis | Spinal And Bulbar Muscular Atrophy | Rhabdomyosarcoma, Alveolar | Incontinentia Pigmenti | Cholecystitis | Cancer, Lung | Acute Motor Axonal Neuropathy | Herpes Genitalis | Glycogen Storage Disease Type 1 | Tietze Syndrome | Palmoplantar Keratoderma | Swine Influenza | Lymphoma, Follicular | Shwachman-Bodian-Diamond Syndrome | Ulcerative Colitis | Arthritis | Agoraphobia | Becker Muscular Dystrophy | Acanthosis Nigricans | Panic Disorder | Spinal Muscular Atrophy Type 3 | Sporadic Inclusion Body Myositis | Venous Insufficiency | Schizophrenia, Paranoid | Sotos Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Vici Syndrome | Vestibular Disease | CDKL5 Deficiency Disorder | Myasthenia | Neutropenia | Pseudohypoparathyroidism Type 1C | Multifocal Motor Neuropathy | Calcium Pyrophosphate Deposition Disease | Familial Male-limited Precocious Puberty | Tuberculosis | Stiff-man Syndrome | Bartter Syndrome | C3 Glomerulopathy | Ollier Disease | Beckwith-Wiedemann Syndrome