Disease

Greenberg Dysplasia

About the Disease
Greenberg Dysplasia, also known as hem dysplasia, is related to smith-lemli-opitz syndrome and x-linked chondrodysplasia punctata 2. An important gene associated with Greenberg Dysplasia is LBR (Lamin B Receptor), and among its related pathways/superpathways are "Cell Cycle, Mitotic" and Separation of Sister Chromatids. Affiliated tissues include bone, pancreatic islet and bone marrow, and related phenotypes are lymphedema and brachydactyly

Common Targets
LBR

疾病靶点研报
Greenberg Dysplasia

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

Other Diseases

Anuria | Glaucomatocyclitic Crisis | Focal Dermal Hypoplasia | Coffin-Siris Syndrome | Calcium Pyrophosphate Deposition Disease | Dystonia | Peters-plus Syndrome | Avian Influenza | Pontocerebellar Hypoplasia Type 2 | Esophageal Motility Disorders | Leber Congenital Amaurosis | Sweet Syndrome | Alazami Syndrome | Syncope | Hyperkalemic Periodic Paralysis | Okihiro Syndrome | Tinea Versicolor | Premenstrual Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Pericarditis | Early Infantile Epileptic Encephalopathy | Desbuquois Syndrome | Kleine-Levin Syndrome | Hypertension, Renal | Adenomyosis | Spinocerebellar Ataxia Type 42 | Familial Hyperaldosteronism | Aldosteronism | Primary Sclerosing Cholangitis | Esophagitis, Eosinophilic | Proopiomelanocortin Deficiency | Synovitis | Nicolaides-Baraitser Syndrome | Blastoma, Pleuropulmonary | Fanconi Anemia | Adenosine Deaminase Deficiency | Cryptococcal Meningitis | Neurodevelopmental Disorders | Hyperinsulinism-hyperammonemia Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Lipoma | Dysgerminoma | Vitreoretinal Degeneration, Snowflake Type | Mucolipidosis Type II | Polyneuropathy | REM Sleep Behavior Disorder | Hypohidrotic Ectodermal Dysplasia | Metachromatic Leukodystrophy | Cartilage Disorders | Congenital Dyserythropoietic Anemia | Globozoospermia | Rothmund-Thomson Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Progressive Osseous Heteroplasia | Facioscapulohumeral Muscular Dystrophy Type 2 | Autoimmune Disease | Pseudoexfoliation Syndrome | High Molecular Weight Kininogen Deficiency | Polydactyly | Thanatophoric Dysplasia | Leber Hereditary Optic Neuropathy | Diabetes Insipidus | Renal-hepatic-pancreatic Dysplasia | Tendinopathy | Eczema | Renal Failure | Ectopia Lentis, Isolated, Autosomal Recessive | Williams Syndrome | Majeed Syndrome | Pulmonary Capillary Hemangiomatosis | Adams-Oliver Syndrome | WAGR Syndrome | Sezary Syndrome | Fetal Akinesia Deformation Sequence | Trimethylaminuria | Palmoplantar Keratoderma | Familial Exudative Vitreoretinopathy | Glaucoma, Congenital | Panuveitis | Antisynthetase Syndrome | Trichotillomania | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Depression | Persistent Fetal Circulation | AIDS Dementia Complex | Tularemia | Cancer, Prostate | Myoclonic Epilepsy With Ragged Red Fibers | Thanatophoric Dysplasia Type 1 | Ellis-Van Creveld Syndrome | Priapism | Spondylometaphyseal Dysplasia | Chondrodysplasia Punctata 2, X-linked Dominant | Bronchiolitis | Long QT Syndrome Type 3 | Hyperparathyroidism, Primary | Heart Septal Defects | Zimmermann-Laband Syndrome | Pilomatrix Carcinoma | Erythrokeratodermia Variabilis | Cholecystitis | Colitis, Collagenous | Cystinosis | Mandibuloacral Dysplasia With Type A Lipodystrophy | Norrie Disease | Aspergillosis | Ureteropelvic Junction Obstruction | Dysferlinopathy | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Jaundice, Obstructive | Growth Hormone Excess | Hamartoma | Polyradiculopathy | Polycystic Kidney, Autosomal Dominant | Myelitis | Pneumoconiosis | DiGeorge Syndrome | Ameloblastic Carcinoma | Sponastrime Dysplasia | Acromesomelic Dysplasia | Meningioma | Becker Muscular Dystrophy | Hypocalcemia | Pseudohypoparathyroidism Type 1A | Spinocerebellar Ataxia | Long QT Syndrome Type 2 | Shwachman-Bodian-Diamond Syndrome | Gigantism | Tonsillitis | Metachondromatosis | Neurofibromatosis-Noonan Syndrome | Opisthorchiasis | Chronic Kidney Disease | Polycystic Liver | Cerebrovascular Disorders | Fahr Disease | Cerebral Cavernous Malformations | Carpal Tunnel Syndrome | X-linked Sideroblastic Anemia | Epithelioid Hemangioma | Lentigo | Charcot-Marie-Tooth Disease, Type 6 | Mitochondrial Myopathy | Cheilitis | Bladder Exstrophy | Persistent Mullerian Duct Syndrome | Creatine Deficiency Syndrome | Nephrotic Syndrome | Familial Retinal Arterial Macroaneurysm | Congenital Lipoid Adrenal Hyperplasia | Rickets | Acute Anterior Uveitis | Urofacial Syndrome | Fibrillation, Atrial | Polycystic Kidney, Autosomal Recessive | Liddle Syndrome | Hyperparathyroidism, Secondary | Retinal Coloboma | Ocular Surface Squamous Neoplasia | Spinal Muscular Atrophy Type 3 | Patent Ductus Arteriosus | Bullous Pemphigoid | Thyrotoxic Periodic Paralysis | Neuronal Ceroid Lipofuscinosis | Pyoderma Gangrenosum | Crouzon Syndrome With Acanthosis Nigricans | Leishmaniasis, Visceral | Stuttering | Nance-Horan Syndrome | LRBA Deficiency | Giant Cell Arteritis | Nephrosclerosis | Tetraplegia | Alkaptonuria | Schizoaffective Disorder | Preaxial Polydactyly | Anovulation | Benign Familial Pemphigus | Rolandic Epilepsy | Benign Recurrent Intrahepatic Cholestasis 1 | Epidermal Nevus Syndrome | Lesch-Nyhan Syndrome | Diabetes Insipidus, Neurogenic | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Corneal Edema | Parapsoriasis | Neuromuscular Disorders | Poikiloderma With Neutropenia | Pyruvate Kinase Deficiency | Charcot-Marie-Tooth Disease, Type 2C | Anal Fissure | Chondrodysplasia Punctata | Mucolipidosis Type IV | Nephronophthisis | Angioedema | Motor Neuron Diseases | Inflammatory Myopathy | Erythropoietic Protoporphyria | Optic Atrophy 2 | Precocious Puberty | Skin Carcinoma | Harlequin Ichthyosis | Colitis, Lymphocytic | CEDNIK Syndrome | Retinitis Pigmentosa | Peroxisomal Disorder | Cockayne Syndrome | Endometriosis | Infertility | Carney Triad | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Vogt-Koyanagi-Harada Syndrome | Congenital Poikiloderma | 3-M Syndrome | Hemochromatosis | Hereditary Coproporphyria | Neutrophilia | Chloridorrhea, Congenital | Budd-Chiari Syndrome | Cone Dystrophy | Schnitzler Syndrome | Anencephaly | Anterior Segment Dysgenesis | Cervical Dystonia | IMAGe Syndrome | Hypertension, Renovascular | Pierpont Syndrome | Gestational Trophoblastic Disease | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Combined Pituitary Hormone Deficiency | Bardet-Biedl Syndrome | Chorea-acanthocytosis | Endometritis | Silicosis | Presbyopia | Porphyria, Variegate | Conn Syndrome | Early Infantile Epileptic Encephalopathy 13 | Odonto-onycho-dermal Dysplasia | Hemolytic Uremic Syndrome, Atypical | Platelet Disorders | Adenoid Cystic Carcinoma | Primary Ovarian Insufficiency | Analgesia | Liver Failure | Danon Disease | Sarcoidosis | Beckwith-Wiedemann Syndrome | Gastric Atrophy | Carcinoma, Squamous Cell | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Chronic Neutrophilic Leukemia | Goiter, Nodular | Alopecia | Mumps | Diamond-Blackfan Anemia | Alopecia Areata | Stroke | Anxiety Disorders | Congenital Heart Defects | Adenoma, Villous | Graft-versus-host Disease | Riboflavin Transporter Deficiency Neuronopathy | Hyperprolactinemia | Nestor-Guillermo Progeria Syndrome | Alveolar Capillary Dysplasia | Antenatal Bartter Syndrome Type 1 | Heart Failure | Pulmonary Tuberculosis | Large Granular Lymphocytic Leukemia | Pontocerebellar Hypoplasia | Macrophagic Myofasciitis | Reflex Epilepsy | Pneumonia, Bacterial | Heart Block | Autism Spectrum Disorders | Carbohydrate Metabolism Disorders | Hypereosinophilic Syndrome | GLUT1 Deficiency Syndrome | Primary Progressive Nonfluent Aphasia | Frontotemporal Dementia | Autosomal Recessive Spastic Paraplegia Type 75 | Hereditary Inclusion Body Myopathy | Spinal Muscular Atrophy Type 2 | Stargardt Disease | Fabry's Disease | Craniofacial Dysostosis | Schwannoma | Greenberg Dysplasia | Muscular Dystrophy | Tumoral Calcinosis | Trachoma | Trichorhinophalangeal Syndrome | Neuroectodermal Tumors, Primitive | Kabuki Syndrome 2 | Hydrocephalus | Porencephaly | Androgenic Alopecia | Ectrodactyly | Vitiligo | Molybdenum Cofactor Deficiency | Necrotizing Autoimmune Myopathy | Kabuki Syndrome | Hypospadias | Myhre Syndrome | Wolff-Parkinson-White Syndrome | Urea Cycle Disorder | Coronary Heart Disease | Lennox-Gastaut Syndrome | Tendinitis | Cranial Nerve Disease | Neurofibromatosis Type 2 | Angioedema, Acquired | Von Willebrand Disease | Scapuloperoneal Spinal Muscular Atrophy | Angiodysplasia | Nephrocalcinosis | Gitelman Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Myotonic Disorders | Colorectal Adenoma | Aromatic L-amino Acid Decarboxylase Deficiency | Familial Hypertrophic Cardiomyopathy | Restless Legs Syndrome | Pregnancy, Ectopic | Rett Syndrome | GNE Myopathy | Cyclic Vomiting Syndrome | Schistosomiasis | Shprintzen-Goldberg Syndrome | Optic Neuropathy, Anterior Ischemic | Waardenburg Syndrome Type 4 | Ocular Hypertension | Syphilis | Acromicric Dysplasia | Hepatitis A | Chronic Mucocutaneous Candidiasis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Benign Familial Infantile Seizures | Osteoglophonic Dysplasia | Japanese Encephalitis | Fraser Syndrome | Eosinophilic Asthma | Primary Erythromelalgia | McKusick Type Metaphyseal Chondrodysplasia | Episodic Ataxia Type 2 | Peritonitis | Holoprosencephaly | Bone Giant Cell Tumor | Agranulocytosis | Hypotonia-cystinuria Syndrome | Uveitis, Anterior | Retinal Dystrophy | Pendred Syndrome | Chondroma | Cole-Carpenter Syndrome | Blood Protein Disorders | Knobloch Syndrome | Melanoma, Malignant | Lipodystrophy | Persistent Truncus Arteriosus | Charcot-Marie-Tooth Disease Type 4D | Acrodermatitis | Nephrotic Syndrome Type 1 | Scoliosis | Potocki-Shaffer Syndrome | Dyskeratosis Congenita | Sick Sinus Syndrome | Fibronectin Glomerulopathy | Hydrolethalus Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Trichothiodystrophy | Anodontia | Perry Syndrome | Congenital Myopathy | Cardiac Arrest | Gastrointestinal Disorders | Hypophosphatasia | Marinesco-Sjogren Syndrome | Heimler Syndrome | Non-Hodgkin Lymphoma | Intermittent Claudication | Apparent Mineralocorticoid Excess Syndrome | Spinocerebellar Ataxia Type 3 | Keratoacanthoma | Ghosal Syndrome | Plasmacytoma | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Woodhouse-Sakati Syndrome | Cutis Laxa | Congenital Mirror Movements | Chromosome 5q Deletion Syndrome | Cholestasis | Neuroleptic Malignant Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Rhizomelic Chondrodysplasia Punctata | Dermatofibrosarcoma | Melanoma | Gardner Syndrome | Distal Myopathy 2