Greenberg Dysplasia
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
Cervicitis | Pendred Syndrome | Lupus Erythematosus | Hypercalciuria | Bicuspid Aortic Valve | Sickle Cell Disease | Xeroderma Pigmentosum Variant Type | Roberts Syndrome | Papilloma | Triple A Syndrome | Spinocerebellar Ataxia Type 12 | Juvenile Polyposis | VACTERL/VATER Association | Basal Ganglia Disease, Biotin-responsive | Lymphoproliferative Disorders | Arthritis, Gouty | Adrenoleukodystrophy, X-linked | Craniopharyngioma | Borjeson-Forssman-Lehmann Syndrome | Branchiootorenal Syndrome | Arthrogryposis | Sclerosing Cholangitis | Spinocerebellar Ataxia Type 23 | Tuberculosis | Nevus | Renal Hypouricemia | Familial Male-limited Precocious Puberty | Polyneuropathy | WAGR Syndrome | Wilson's Disease | Pseudo-pseudohypoparathyroidism | Gaucher Disease | Pituitary Dwarfism | Thrombophlebitis | Chorea-acanthocytosis | Bladder Exstrophy | Heart Block | Liddle Syndrome | Obesity | Lathosterolosis | Combined Deficiency Of Factor V And Factor VIII | Pierpont Syndrome | Enlarged Vestibular Aqueduct | Carcinoma, Signet Ring Cell | Gingivitis | Heimler Syndrome | Holt-Oram Syndrome | Hypertension, Portal | Bardet-Biedl Syndrome | Fahr Disease | Osteogenesis Imperfecta Type IV | Graft-versus-host Disease | Epidermolysis Bullosa Simplex | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Neural Tube Defect | Aceruloplasminemia | Sepiapterin Reductase Deficiency | Juvenile Myoclonic Epilepsy | Corticobasal Syndrome | Bloom Syndrome | Dowling-Degos Disease | Juvenile Myelomonocytic Leukemia | Unverricht-Lundborg Syndrome | Chediak-Higashi Syndrome | Choroiditis | Conduct Disorder | Hashimoto Thyroiditis | Paronychia | Pierre Robin Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Mesothelioma, Malignant | Palsy, Cerebral | Leukocyte Adhesion Deficiency | Shwachman-Bodian-Diamond Syndrome | Borderline Personality Disorder | CHOPS Syndrome | Costello Syndrome | Alagille Syndrome | Menetrier Disease | Oral Lichen Planus | Vitiligo | Hamartoma | Aneurysm, Thoracic Aortic | Alpha-1 Antitrypsin Deficiency | Urticaria | Melanoma, Malignant | Lymphangioma | HANAC Syndrome | Spondylosis | Autoimmune Hemolytic Anemia | Cancer, Brain | Liver Failure, Acute Infantile | Stevens-Johnson Syndrome | Chiari Malformation Type I | Hodgkin Lymphoma | Angioedema | Lymphangioleiomyomatosis | Peeling Skin Syndrome Type B | Kaposiform Hemangioendothelioma | Retinitis Pigmentosa 3 | Atrial Septal Defect | Kohlschutter-Tonz Syndrome | Leukoplakia | Apparent Mineralocorticoid Excess Syndrome | Carpenter Syndrome | Congestive Heart Failure | Epidermolysis Bullosa | Wieacker-Wolff Syndrome | Paget's Disease Of The Breast | Johanson-Blizzard Syndrome | Benign Familial Pemphigus | Bullous Pemphigoid | HELLP Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Globozoospermia | X-linked Sideroblastic Anemia | Bulimia Nervosa | Vitreoretinal Degeneration, Snowflake Type | Fetal And Neonatal Alloimmune Thrombocytopenia | Retinopathy Of Prematurity | Li-Fraumeni Syndrome | X-linked Charcot-Marie-Tooth Disease | Veno-occlusive Disease | Chondromyxoid Fibroma | Ureteropelvic Junction Obstruction | Osteitis | Leukocyte Adhesion Deficiency Type 1 | Auriculocondylar Syndrome | Hepatoblastoma | Craniosynostosis | Peritonitis | Lymphangiomatosis | Still Disease | Scoliosis | Anencephaly | Parapsoriasis | ACTH-independent Macronodular Adrenal Hyperplasia | Familial Retinal Arterial Macroaneurysm | Generalized Epilepsy And Paroxysmal Dyskinesia | Kidney Stones | Klinefelter Syndrome | Tic Disorder | Antisocial Personality Disorder | Ichthyosis Hystrix, Curth-Macklin Type | Renal Failure | Cyst | Melanoma, Uveal | Osteopetrosis | Oguchi Disease-2 | Myositis, Focal | Periventricular Nodular Heterotopia | Endophthalmitis | Hyperlipidemia, Familial Combined | Light Chain Amyloidosis | Lattice Corneal Dystrophy Type 1 | Perry Syndrome | Cutaneous Mastocytosis | Optic Neuropathy, Anterior Ischemic | Bone Giant Cell Tumor | CEDNIK Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Hereditary Sensory And Autonomic Neuropathy | Diabetes | Myofibrillar Myopathy | Lichen Planus | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Ataxia-ocular Apraxia 2 | Jawad Syndrome | MELAS Syndrome | Congenital Central Hypoventilation Syndrome | Mucolipidosis Type II | Epidermolysis Bullosa Dystrophica | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Burn-McKeown Syndrome | Synpolydactyly | Allergic Contact Dermatitis | Malaria | Epidermolysis Bullosa Simplex, Generalized | Epidermodysplasia Verruciformis | Hypokalemia | Keratitis | Takayasu's Arteritis | Carcinoma, Merkel Cell | Lysosomal Acid Lipase Deficiency | Transthyretin-related Amyloidosis | Marshall-Smith Syndrome | Hypothyroidism | Stroke, Ischemic | Trimethylaminuria | Gerstmann-Straussler-Scheinker Syndrome | Pituitary Disorders | Fundus Albipunctatus | Osteomalacia | Ophthalmoplegia | Dystonia-parkinsonism, X-linked | Tricho-hepato-enteric Syndrome | Goiter, Nodular | Acrodysostosis | Neurotoxicity | Dentinogenesis Imperfecta | Aphasia | Eczema | H Syndrome | Birk-Barel Syndrome | Multiple System Atrophy | Overactive Bladder | Large Granular Lymphocytic Leukemia | Contact Dermatitis | Epidermolytic Hyperkeratosis | Oligospermia | Proctitis | Babesiosis | Pernicious Anemia | Walker-Warburg Syndrome | Pyoderma Gangrenosum | Chronic Leukemia | Pyruvate Kinase Deficiency | Arthritis, Psoriatic | Chromosome 9q34.3 Deletion Syndrome | Sarcoidosis | Thin Basement Membrane Disease | Poikiloderma With Neutropenia | Tendinitis | Chondrodysplasia Punctata | Birt-Hogg-Dube Syndrome | Metachromatic Leukodystrophy | Thalassemia | Focal Segmental Glomerulosclerosis | Blepharoconjunctivitis | Frontometaphyseal Dysplasia | Nephroblastoma | Retinal Dystrophy, Early-onset Severe | Hereditary Multiple Exostoses | Usher Syndrome Type IIC | Gyrate Atrophy Of The Choroid And Retina | Primary Torsion Dystonia | ICF Syndrome | Leri Pleonosteosis | Pilomatrix Carcinoma | Warsaw Breakage Syndrome | Papillon-Lefevre Syndrome | Hypoplastic Left Heart Syndrome | Thyroiditis, Autoimmune | Carney Triad | Hepatitis A | Klippel-Feil Syndrome | Optic Atrophy 2 | Proteasome-associated Autoinflammatory Syndrome 2 | Blau Syndrome | Anorectal Fistula | Donnai-Barrow Syndrome | Hypermetropia | Keratosis, Actinic | Pneumothorax | Infantile Liver Failure Syndrome 1 | Neutrophilia | Spinocerebellar Ataxia Type 15 | Reticular Dysgenesis | Bacterial Meningitis | Hemophilia | Hyperandrogenemia | Polyradiculopathy | Pleurisy | Chylomicron Retention Disease | Bartter Syndrome | Synovitis | Relapsing Polychondritis | Hyperoxaluria | Lennox-Gastaut Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Olmsted Syndrome | Gilbert Syndrome | Pyruvate Carboxylase Deficiency Disease | Nephrocalcinosis | Gastritis | Hermansky-Pudlak Syndrome | Peters-plus Syndrome | Crisponi Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Congenital Afibrinogenemia | Thrombotic Microangiopathy | Meningioma | Cardiomyopathy, Restrictive | Intestinal Pseudo-obstruction | Myositis | Pseudohypoparathyroidism Type 1C | Salla Disease | Lentigo | Cerebral Amyloid Angiopathy | Fontaine Progeroid Syndrome | Waardenburg Syndrome Type 2 | Encephalopathy, Glycine | Cancer, Prostate | Episodic Ataxia | Pulmonary Veno-occlusive Disease | Sick Sinus Syndrome | Mastitis | Methylmalonic Acidemia | Keloid | Hemolytic Uremic Syndrome, Atypical | Ectrodactyly | Chordoma | LMNA-related Congenital Muscular Dystrophy | Haim-Munk Syndrome | Hydrocephalus | Renal Tubular Dysgenesis | Peripheral T-cell Lymphoma | Epilepsy Of Infancy With Migrating Focal Seizures | Cartilage Disorders | Stroke, Hemorrhagic | Benign Hereditary Chorea | Long QT Syndrome Type 3 | Necrotizing Autoimmune Myopathy | Amenorrhea | TARP Syndrome | Osteosarcoma | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Teratozoospermia | Whipple's Disease | Hypoalbuminemia | Pfeiffer Syndrome | Werner's Syndrome | Pleural Tuberculosis | Lymphoma, AIDS-related | Venous Insufficiency | Papillorenal Syndrome | Beckwith-Wiedemann Syndrome | Rotor Syndrome | Hemorrhage | Intermittent Claudication | Eccrine Porocarcinoma | Vitreoretinopathy, Proliferative | Urofacial Syndrome | Canavan Disease | Panuveitis | Hypertension, Essential | Melanocytic Nevus | Histiocytosis | Megaloblastic Anemia | Thanatophoric Dysplasia Type 1 | Microvillus Inclusion Disease | Porokeratosis | Congenital Bile Acid Synthesis Defect | Colon Adenoma | Neurofibroma, Plexiform | Neuroma | Non-Hodgkin Lymphoma | Lymphopenia | Peroxisomal Disorder | Congenital Lipoid Adrenal Hyperplasia | Blue Nevus | Inflammatory Myofibroblastic Tumor | Leukoplakia, Oral | Acute Coronary Syndrome | Emery-Dreifuss Muscular Dystrophy | Epiphyseal Chondrodysplasia, Miura Type | Neurodegeneration With Brain Iron Accumulation | Kaposi Sarcoma | Lipid Metabolism Disorders | Diabetic Nephropathy | Congenital Disorders Of Glycosylation Type II | Postpartum Depression | Leukemia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Monilethrix | Asthma, Exercise-induced | Familial Pheochromocytoma-paraganglioma | Leishmaniasis, Visceral | Gangliosidosis, GM1 | Sorsby Fundus Dystrophy | Diabetes Insipidus, Neurogenic | Supravalvular Aortic Stenosis | Scleritis | Thyroid Hormone Resistance | Idiopathic Pulmonary Fibrosis | Central Retinal Artery Occlusion | Charcot-Marie-Tooth Disease Type 4D | Parkinson's Disease | Crigler-Najjar Syndrome | Cutaneous T-cell Lymphoma | Idiopathic Multicentric Castleman Disease | Atopy | Episodic Ataxia Type 2 | Mountain Sickness | Colorectal Adenoma | Chronic Kidney Disease | Toxoplasmosis | Lassa Fever | Corneal Edema | Sweet Syndrome | Plasmacytoma | Fibrodysplasia Ossificans Progressiva | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Osteogenesis Imperfecta Type V | Hyperferritinemia-cataract Syndrome | Nance-Horan Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Esophageal Adenocarcinoma | Hepatitis, Autoimmune | Alkaptonuria