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

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

Sick Sinus Syndrome 1 | Tendinitis | Milk Allergy | Cholelithiasis | Hypopituitarism | Vitreoretinopathy, Proliferative | Communication Disorders | Fibrosarcoma | Crouzon Syndrome With Acanthosis Nigricans | Hashimoto Thyroiditis | Venous Insufficiency | Hypotrichosis | Cystitis, Interstitial | Anal Fissure | Phenylketonuria | Aplastic Anemia | Fraser Syndrome | Leiomyosarcoma | Leigh Syndrome | Spastic Paraplegia Type 7 | Intermittent Explosive Disorder | Sleep Apnea | Burn-McKeown Syndrome | Hypoalbuminemia | ICF Syndrome | Ophthalmoplegia | Shock, Cardiogenic | Microvillus Inclusion Disease | Ataxia-ocular Apraxia 2 | Chudley-McCullough Syndrome | Hyperglycemia | Esophageal Carcinoma | Hypertensive Nephropathy | Primary Hyperoxaluria | Mesothelioma, Malignant | Multiple Hamartoma Syndrome | Vitamin B12 Deficiency | Oculocutaneous Albinism Type 1 | Opisthorchiasis | Charcot-Marie-Tooth Disease Type 2D | Loeys-Dietz Syndrome Type 4 | Sarcoidosis, Pulmonary | Riboflavin Transporter Deficiency Neuronopathy | Leukoplakia | Sclerosing Cholangitis | Neurofibroma | Carcinoid Syndrome | Neuroleptic Malignant Syndrome | Esthesioneuroblastoma | 3C Syndrome | Epithelial-myoepithelial Carcinoma | Chondrodysplasia Punctata 1, X-linked Recessive | Transient Bullous Dermolysis Of The Newborn | Ebstein Anomaly | Blue Nevus | Hypertension, Portal | Spondylosis | Prediabetes | Dystonia Musculorum Deformans | Fetal And Neonatal Alloimmune Thrombocytopenia | Pneumoconiosis | Mitochondrial Myopathy | Odonto-onycho-dermal Dysplasia | Persistent Truncus Arteriosus | Meniere's Disease | Charcot-Marie-Tooth Disease | Salla Disease | Metanephric Adenoma | Adenoma, Pituitary | Adult Polyglucosan Body Disease | H Syndrome | Thin Basement Membrane Disease | Congenital Disorders Of Glycosylation Type II | Hepatitis | Gallstones | Herpes Genitalis | Colitis, Lymphocytic | Disseminated Intravascular Coagulation | Familial Hypertrophic Cardiomyopathy | Alexander Disease | Chordoma | Diabetes Insipidus | Congenital Nephrotic Syndrome | Knobloch Syndrome | Blomstrand Osteochondrodysplasia | Turner's Syndrome | Neurotoxicity | Giant Cell Arteritis | Cleidocranial Dysplasia | Azoospermia | Cutaneous Angiosarcoma | Antisocial Personality Disorder | Split Hand-foot Malformation | Episodic Ataxia | Pseudohypoparathyroidism Type 2 | Seizures | Diabetes Insipidus, Nephrogenic | Budd-Chiari Syndrome | Endometritis | Polyneuropathy | VACTERL/VATER Association | Osmotic Demyelination Syndrome | Heart Septal Defects | Melanoma, Malignant | Varices | Congenital Stationary Night Blindness | Cheilitis | Cervical Dystonia | Low Tension Glaucoma | Acute Lymphocytic Leukemia | Congenital Adrenal Hyperplasia 1 | Benign Familial Infantile Seizures | Familial Advanced Sleep Phase Syndrome | Vertigo | Ollier Disease | Antiphospholipid Syndrome | Chitayat Syndrome | Barakat Syndrome | Von Willebrand Disease | Oligodendroglioma | Brenner Tumor | Osteonecrosis Of The Jaw | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Dystrophy, Cone-rod | Measles | Congenital Bile Acid Synthesis Defect | Osteoglophonic Dysplasia | Coloboma | LRBA Deficiency | Liver Failure | Central Pain Syndrome | Tyrosinemia | Cri-du-chat Syndrome | Congenital Hemolytic Anemia | Mitochondrial DNA Depletion Syndrome 13 | Genitopatellar Syndrome | Muir-Torre Syndrome | Hemolytic Uremic Syndrome, Atypical | Mohr-Tranebjaerg Syndrome | Reflex Epilepsy | Synpolydactyly | Danon Disease | Cole-Carpenter Syndrome | Pneumonia, Mycoplasma | Monilethrix | Learning Disability | Arthritis, Reactive | Cholera | GNE Myopathy | Waardenburg Syndrome Type 2 | Inflammatory Linear Verrucous Epidermal Nevus | Spinocerebellar Ataxia Type 2 | Tardive Dyskinesia | Loeys-Dietz Syndrome | Restrictive Dermopathy | C3 Glomerulopathy | Castleman Disease | Congenital Hereditary Endothelial Dystrophy Type II | Language Disorders | Congenital Adrenal Hyperplasia | Keratosis | Cancer, Prostate | Autoimmune Polyendocrinopathy Syndrome Type I | Leishmaniasis, Cutaneous | Lymphoma, AIDS-related | Methylmalonic Aciduria And Homocystinuria, CblC Type | Esophageal Adenocarcinoma | Blau Syndrome | Hyperacusis | Cone Dystrophy | Impulse Control Disorder | Neurocutaneous Melanocytosis | Apparent Mineralocorticoid Excess Syndrome | Batten Disease | Fatty Aldehyde Dehydrogenase Deficiency | Persistent Mullerian Duct Syndrome | Anorchia | Primary Torsion Dystonia | Triple A Syndrome | Dermatomyositis | PHARC Syndrome | Chronic Beryllium Disease | Cardiofaciocutaneous Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Thrombocytopenia | Hereditary Mixed Polyposis Syndrome | Dyslipidemia | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Optic Nerve Diseases | Lung Diseases | Thrombophlebitis | Granuloma Annulare | Diabetic Encephalopathy | Endophthalmitis | Atrioventricular Septal Defect | Rosacea | Glaucomatocyclitic Crisis | Lentigo | Cholangitis | Shwachman-Bodian-Diamond Syndrome | Osteopathia Striata With Cranial Sclerosis | Glucagonoma | Twin-to-twin Transfusion Syndrome | Hereditary Elliptocytosis | Rheumatic Heart Disease | Vestibular Disease | Tendinopathy | Irritable Bowel Syndrome | COACH Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Cataract | Aldosterone Synthase Deficiency | Spinocerebellar Ataxia Type 10 | Spermatocele | Spinocerebellar Ataxia Type 7 | Hyperlipidemia Type V | Schistosomiasis | Episodic Ataxia Type 1 | Lafora Disease | Fibromuscular Dysplasia | Sarcoma, Ewing | Common Variable Immunodeficiency | Trigonocephaly | Primary Progressive Nonfluent Aphasia | Hemochromatosis Type 1 | Waldenstrom Macroglobulinemia | Deafness, Dystonia, And Cerebral Hypomyelination | Carbamoyl Phosphate Synthetase I Deficiency | Miyoshi Myopathy | Greig Cephalopolysyndactyly Syndrome | Basan Syndrome | Cystitis | Poirier-Bienvenu Neurodevelopmental Syndrome | Ischemia | Congenital Muscular Dystrophy | Primary Pigmented Nodular Adrenocortical Disease | Specific Granule Deficiency | Lymphoproliferative Disease, X-linked | Camptocormia | Waardenburg Syndrome Type 2E | Spina Bifida | Epidermolysis Bullosa | Cysticercosis | Gangliosidosis, GM1 | Osteosclerosis | Heroin Dependence | Blue Rubber Bleb Nevus Syndrome | Osteoarthritis | Hypercholesterolemia | Focal Segmental Glomerulosclerosis | Greenberg Dysplasia | Glutaric Aciduria Type 1 | Renal Failure | X-linked Myotubular Myopathy | Peutz-Jeghers Syndrome | Coronary Heart Disease | Epidermodysplasia Verruciformis | Encephalitis | Metachondromatosis | Sarcoma, Alveolar Soft Part | Thrombasthenia | Congestive Heart Failure | Spinal And Bulbar Muscular Atrophy | Gerstmann-Straussler-Scheinker Syndrome | Trichorhinophalangeal Syndrome | Corticobasal Syndrome | X-linked Sideroblastic Anemia | Myopia | Hepatitis B, Chronic | Congenital Aniridia | Epilepsy Of Infancy With Migrating Focal Seizures | Uveitis | Trichothiodystrophy | Precocious Puberty | Weill-Marchesani Syndrome | Poretti-Boltshauser Syndrome | Thrombocythemia, Essential | Hydrocephalus | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Paget's Disease Of The Breast | Sickle Cell Disease | Bronchitis, Chronic | Tremor | Moyamoya Disease | Sporadic Inclusion Body Myositis | Chronic Mucocutaneous Candidiasis | Retinal Degeneration | Hermansky-Pudlak Syndrome | Best Macular Dystrophy | Conjunctivitis, Allergic | Blepharoconjunctivitis | Arterial Tortuosity Syndrome | Corneal Dystrophy | Alpha-mannosidosis | Meningitis | Optic Atrophy 2 | Bruck Syndrome | Carcinoma, Transitional Cell | Epicondylitis | Double Outlet Right Ventricle | Hypoparathyroidism | Optic Nerve Hypoplasia, Bilateral | Long QT Syndrome Type 1 | Cold-induced Sweating Syndrome | Myelitis | Plasma Cell Leukemia | Distal Myopathy 2 | Thalassemia, Beta | Hypercalcemia | Schistosomiasis Mansoni | Hepatitis, Autoimmune | Pachyonychia Congenita | Hyperuricemic Nephropathy, Familial Juvenile | Dysfibrinogenemia | Proteasome-associated Autoinflammatory Syndrome 2 | Central Core Disease | Thrombosis | Hereditary Pyropoikilocytosis | Thyrotoxic Periodic Paralysis | Colitis, Microscopic | Acanthosis Nigricans | Anthrax | Spinocerebellar Ataxia Type 3 | Coffin-Siris Syndrome | Pityriasis Rubra Pilaris | Acute Anterior Uveitis | Pseudohypoparathyroidism Type 1A | Congenital Stromal Corneal Dystrophy | Spasticity | Cardiomyopathy, Dilated, 1L | Glycogen Storage Disease Type 1b | Autism Spectrum Disorders | Trismus-pseudocamptodactyly Syndrome | Cartilage Disorders | Trichuriasis | Left Ventricular Noncompaction | Infertility | Aicardi-Goutieres Syndrome | Eosinophilia | Congenital Poikiloderma | Obesity | Sertoli Cell-only Syndrome | Corneal Dystrophy And Perceptive Deafness | Cirrhosis | Sengers Syndrome | Pseudomyxoma Peritonei | Shprintzen-Goldberg Syndrome | Cockayne Syndrome | Blastoma, Pleuropulmonary | Carpal Tunnel Syndrome | Tyrosinemia Type 2 | Carcinoma In Situ | Netherton Syndrome | Acute Tubular Necrosis | Lymphomatoid Granulomatosis | Binge Eating Disorder | Cardiomyopathy, Peripartum | Gout | Amblyopia | Keratoconus | Albinism | Fuchs Dystrophy | Incontinentia Pigmenti | Aneurysm, Abdominal Aortic | Menetrier Disease | Oculopharyngeal Muscular Dystrophy | Angiomyolipoma | Methylmalonic Acidemia | Kaposi Sarcoma | Hemochromatosis | Goiter, Nodular | Encephalocele | Alopecia Totalis | Birt-Hogg-Dube Syndrome | Diffuse Intrinsic Pontine Glioma | Vitamin A Deficiency | D-2-Hydroxyglutaric Aciduria | Kashin-Beck Disease | Heterotaxy | Mannosidase Deficiency Diseases | Acrodysostosis | Congenital Diaphragmatic Hernia | Arthropathy | Diabetic Macular Edema | Methemoglobinemia Type IV | Stroke, Ischemic | Ganglioglioma | Urolithiasis | Spinal Muscular Atrophy Type 3 | Anxiety Disorders | Menkes Disease | Van Der Knaap Disease | Cholesteryl Ester Storage Disease | Pyruvate Carboxylase Deficiency Disease | Autosomal Recessive Spastic Paraplegia Type 75 | Colitis, Collagenous | Diarrhea | Muscular Dystrophy | Kallmann Syndrome | Werner's Syndrome