Disease

Osteopetrosis

About the Disease
Osteopetrosis, also known as marble bone disease, is related to osteopetrosis, autosomal recessive 7 and osteopetrosis, autosomal recessive 5. An important gene associated with Osteopetrosis is CLCN7 (Chloride Voltage-Gated Channel 7), and among its related pathways/superpathways are Innate Immune System and Akt Signaling. The drugs Cyclophosphamide and Fludarabine have been mentioned in the context of this disorder. Affiliated tissues include bone, bone marrow and spleen, and related phenotypes are no effect and no effect

Common Targets
PTGER2 | PLA2G2A | Histone deacetylase (nonspecified subtype) | LEMD3 | cAMP Phosphodiesterase (nonspecified subtype) | JAK3 | GAPDH | G1956 | MIR23A | SOST | G7124 | SNX10 | IFNGR1 | CA1 | G6774 | CA12 | IKBKG | MC2R | CTSL | LRP5 | CASR | PLEKHM1 | TRAF6 | ENG | TNFSF11 | ESR2 | GLO1 | SLC29A3 | CA7 | Estrogen receptor (nonspecified subtype) | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | FERMT3 | ESRRA | ACVRL1 | CSNK1A1 | PTH | TCIRG1 | TNFRSF11A | PTGER4 | MIR214 | SGMS2 | G2099 | CTSK | PLA2G2D | CA9 | Phospholipase A2, Secretory (sPLA2) (nonspecified subtype) | CA2 | G196 | SGMS1 | SLC6A4 | PDE5A | APP | CLCN7 | OSTM1 | P2RX7 | VDR | OSCAR

疾病靶点研报
Osteopetrosis

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

Other Diseases

Familial Hypobetalipoproteinemia | Infantile Spasm | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Vitamin K Deficiency | Nephritis, Interstitial | Lupus Erythematosus | DOCK8 Immunodeficiency Syndrome | Lymphoproliferative Disease, X-linked | Feingold Syndrome | Asphyxia Neonatorum | Anorectal Malformations | Biotinidase Deficiency | Primary Familial Brain Calcification | Distal Myopathy 2 | Basal Ganglia Cerebrovascular Disease | Urticaria | Bronchiectasis | Contact Dermatitis | Communication Disorders | Pregnancy, Ectopic | Osteoarthritis | Congenital Bile Acid Synthesis Defect | Congenital Adrenal Hyperplasia 1 | Desmosterolosis | Cherubism | Chylomicron Retention Disease | Migraine | Pituitary Dwarfism | DRESS Syndrome | Camptocormia | Acanthosis Nigricans | Familial Hyperaldosteronism | Thrombocytopenia | Benign Familial Pemphigus | Pachyonychia Congenita | Tricho-hepato-enteric Syndrome | Encephalopathy, Glycine | Erdheim-Chester Disease | Language Disorders | Erectile Dysfunction | Primary Sclerosing Cholangitis | Benign Recurrent Intrahepatic Cholestasis 1 | Thrombophilia | Dysplastic Nevus | Porphyria, Acute Intermittent | Chediak-Higashi Syndrome | Acne | Jacobsen Syndrome | Keratoconjunctivitis | Neurofibromatosis Type 2 | Benign Familial Infantile Seizures | Hyper IgE Syndrome | IgA Deficiency | Epidermal Nevus Syndrome | Globozoospermia | Congenital Hypofibrinogenemia | Mumps | Central Pain Syndrome | MIRAGE Syndrome | Osteopathia Striata With Cranial Sclerosis | Mesothelioma, Malignant | Thanatophoric Dysplasia | Myoclonic Atonic Epilepsy | Pathological Gambling | Mucolipidosis Type III | Holoprosencephaly | Stroke, Hemorrhagic | Pure Red Cell Aplasia | Vitiligo | Spinocerebellar Ataxia Type 10 | Pseudo-pseudohypoparathyroidism | Lymphedema-distichiasis Syndrome | Steel Syndrome | Leukemia-lymphoma, Adult T-cell | Gigantism | Cancer, Kidney | Budd-Chiari Syndrome | Glycogen Storage Disease Type 4 | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Uveitis, Anterior | Gerstmann-Straussler-Scheinker Syndrome | Relapsing Polychondritis | Hypertriglyceridemia | Obesity, Morbid | Angiomyolipoma | Hypervalinemia | Poretti-Boltshauser Syndrome | Neuropathy | Vulvovaginitis | Pseudohermaphroditism | Necrotizing Autoimmune Myopathy | Hyperekplexia | Carcinoma, Signet Ring Cell | Alagille Syndrome | CREST Syndrome | Sorsby Fundus Dystrophy | Osmotic Demyelination Syndrome | Rheumatoid Arthritis | Filariasis | Pantothenate Kinase-associated Neurodegeneration | Scleroderma, Diffuse | Erythema Multiforme | Pernicious Anemia | Polyradiculopathy | Giant Axonal Neuropathy | Prolactinoma | AIDS Dementia Complex | Motion Sickness | Congenital Stationary Night Blindness | Farber Disease | Progressive Osseous Heteroplasia | Donnai-Barrow Syndrome | Periodontitis | Keratoconus | Opisthorchiasis | Norrie Disease | Charcot-Marie-Tooth Disease Type 4B1 | Charcot-Marie-Tooth Disease Axonal Type 2N | Aphasia | Polydactyly | Adenocarcinoma | Miyoshi Myopathy | Retinal Dystrophy, Early-onset Severe | Otitis Media | Aicardi-Goutieres Syndrome | Pleomorphic Xanthoastrocytoma | Pierre Robin Syndrome | Multiple Sclerosis, Primary Progressive | Christianson Syndrome | Neovascular Glaucoma | Adrenomyeloneuropathy | Coronary Artery Disease | Episodic Ataxia Type 1 | Guttate Psoriasis | Primary Erythromelalgia | Chronic Thromboembolic Pulmonary Hypertension | Wagner Disease | Platelet Disorders | Follicular Dendritic Cell Sarcoma | Urethritis | Hepatic Adenomatosis | Pyloric Stenosis, Infantile Hypertrophic | Larsen Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Uveitis | Spinocerebellar Ataxia Type 14 | Kawasaki Disease | Necrobiosis Lipoidica | LMNA-related Congenital Muscular Dystrophy | Corneal Dystrophy And Perceptive Deafness | Benign Familial Neonatal Convulsions | H Syndrome | Bethlem Myopathy | Angioedema | Swine Influenza | Primary Hyperoxaluria | Choriocarcinoma | Hypertension | Chromosome 16p11.2 Deletion Syndrome | Familial Hypertrophic Cardiomyopathy | Multicentric Carpotarsal Osteolysis Syndrome | Pyruvate Carboxylase Deficiency Disease | Babesiosis | Hemolytic Uremic Syndrome, Atypical | Acute Generalized Exanthematous Pustulosis | Calcium Pyrophosphate Deposition Disease | Leukoplakia | Cousin Syndrome | Osteomyelitis | Myasthenia Gravis | Kearns-Sayre Syndrome | Actinomycetoma | Dent Disease | Persistent Hyperplastic Primary Vitreous | Onchocerciasis | Sepiapterin Reductase Deficiency | Early Infantile Epileptic Encephalopathy 28 | Joubert Syndrome 2 | Rotor Syndrome | Periodic Limb Movement Disorder | Hyperglycemia | Sarcoidosis, Pulmonary | Progressive Familial Intrahepatic Cholestasis | Hemolytic Uremic Syndrome | 3-methylglutaconic Aciduria | Hemoglobinopathies | Spinocerebellar Ataxia Type 23 | Autoimmune Autonomic Ganglionopathy | Non-Hodgkin Lymphoma | Focal Facial Dermal Dysplasia | Vertebrobasilar Insufficiency | Kashin-Beck Disease | Spinocerebellar Ataxia Type 42 | Leukoencephalopathy, Progressive Multifocal | Myelodysplasia | Learning Disability | Gaucher Disease | Congenital Lipoid Adrenal Hyperplasia | Creutzfeldt-Jakob Disease | Exfoliative Dermatitis | Acrodysostosis | Chanarin-Dorfman Syndrome | Pulmonary Veno-occlusive Disease | Pemphigus | GM2-gangliosidosis AB Variant | Thrombasthenia | Congenital Torticollis | Epidermolysis Bullosa Acquisita | Congenital Fiber-type Disproportion Myopathy | Dyskeratosis Congenita | Lymphoma Lymphoblastic | Antenatal Bartter Syndrome Type 1 | Glycogen Storage Disease Type 1a | Cardiomyopathy, Hypertrophic | Open-angle Glaucoma | Lymphoma, B-cell | Neurofibromatosis-Noonan Syndrome | Renal Oncocytoma | Retinitis Pigmentosa 3 | Hypereosinophilic Syndrome | Microcephaly, Seizures, And Developmental Delay | Primary Biliary Cholangitis | Neuroleptic Malignant Syndrome | Atrial Septal Defect | Spondyloepiphyseal Dysplasia Tarda, X-linked | Sjogren Syndrome | Frontotemporal Dementia | Vitreoretinal Degeneration, Snowflake Type | Gardner Syndrome | Succinic Semialdehyde Dehydrogenase Deficiency | Exostoses | Myhre Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Carey-Fineman-Ziter Syndrome | Renal-hepatic-pancreatic Dysplasia | Spondylometaphyseal Dysplasia | Lennox-Gastaut Syndrome | Ebstein Anomaly | Geleophysic Dysplasia | Colitis, Microscopic | Spinocerebellar Ataxia Type 28 | Carcinoma In Situ | Myelofibrosis | Osteoporosis-pseudoglioma Syndrome | Gastritis, Atrophic | Sotos Syndrome | Tinea Versicolor | Behcet's Disease | Microtia | Hemosiderosis | Acral Lentiginous Melanoma | Conn Syndrome | Sclerosteosis | NGLY1 Deficiency | Panic Disorder | Myopia | Encephalitis, Tick-borne | Spitzoid Melanoma | Amblyopia | Infantile Liver Failure Syndrome 1 | Rett Syndrome | Prediabetes | Syndactyly | Left Ventricular Noncompaction | Occipital Neuralgia | Liver Failure | Mastitis | Meckel-Gruber Syndrome | T-cell Chronic Lymphocytic Leukemia | Immunoproliferative Disorders | Becker Muscular Dystrophy | NDH Syndrome | Wolfram Syndrome 2 | Familial Exudative Vitreoretinopathy | Growth Hormone Excess | Autosomal Recessive Spastic Paraplegia Type 75 | Hyperbilirubinemia, Neonatal | Mucormycosis | Ureteropelvic Junction Obstruction | Progressive Familial Intrahepatic Cholestasis Type 1 | Asthma, Nocturnal | Diabetes Insipidus, Neurogenic | Congenital Dysfibrinogenemia | Chondrodysplasia Punctata 2, X-linked Dominant | Myotonia | Autonomic Nervous System Disorders | Cutaneous Angiosarcoma | Nasodigitoacoustic Syndrome | Influenza | Isobutyryl-CoA Dehydrogenase Deficiency | Corneal Dystrophies, Hereditary | Tic Disorder | Nephroblastoma | Transthyretin-related Amyloidosis | T-cell Lymphoma, Subcutaneous Panniculitis-like | Multifocal Motor Neuropathy | Familial Episodic Pain Syndrome | Bladder Exstrophy | Carcinoma, Small Cell | Glycogen Storage Disease Type 9 | Spasticity | Congenital Heart Block | Congenital Dyserythropoietic Anemia Type 1 | Pyruvate Decarboxylase Deficiency | Patent Ductus Arteriosus | Lymphangioma | Glomerulonephritis | Kallmann Syndrome | Primary Aldosteronism | Hemochromatosis Type 2 | Tatton-Brown-Rahman Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Mucolipidosis Type IV | Hemangioendothelioma | Chronic Periodontitis | Osteosarcoma | Congenital Adrenal Hyperplasia | Parkinsonism | Pain | Prolidase Deficiency | Spinocerebellar Ataxia Type 13 | Diffuse Palmoplantar Keratoderma | Sezary Syndrome | Odonto-onycho-dermal Dysplasia | Cutaneous Lupus Erythematosus | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Chronic Granulomatous Disease, X-linked | Lymphoma | Corneal Ulcer | Fucosidosis | Osteogenesis Imperfecta Type V | Glanzmann Thrombasthenia | B-cell Chronic Lymphocytic Leukemia | Corneal Neovascularization | Oligoastrocytoma | Fetal Alcohol Syndrome | Dyslexia | Infectious Diarrhea | Neutropenia | Vici Syndrome | Trismus-pseudocamptodactyly Syndrome | Achromatopsia | Lattice Corneal Dystrophy | Dystonia Musculorum Deformans | Currarino Syndrome | Veno-occlusive Disease | Supravalvular Aortic Stenosis | Dupuytren Disease | Early Infantile Epileptic Encephalopathy 4 | Ischemia | Lymphangioleiomyomatosis | Cryptorchidism | Purpura, Thrombotic Thrombocytopenic | Intermittent Explosive Disorder | Brenner Tumor | Asperger Syndrome | Osteochondroma | Tardive Dyskinesia | Alcoholism | Macrodactyly | Spastic Paraplegia Type 7 | Poirier-Bienvenu Neurodevelopmental Syndrome | Unverricht-Lundborg Syndrome | Acrocallosal Syndrome | Joubert Syndrome | Hepatic Steatosis | Pouchitis | Empyema | Dementia | Ulcerative Colitis | Omenn Syndrome | Peritonitis | Gastroenteritis, Eosinophilic | Schwartz-Jampel-Aberfeld Syndrome | Specific Granule Deficiency | Spinocerebellar Ataxia Type 5 | Hypoglycemia | Klippel-Feil Syndrome | Still Disease | Li-Fraumeni Syndrome | Granular Corneal Dystrophy Type 1 | Prurigo Nodularis | Lissencephaly 2 | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Seizures | 5-oxoprolinase Deficiency | Dowling-Degos Disease | Nicolaides-Baraitser Syndrome | Spinocerebellar Ataxia Type 21 | Metanephric Adenoma | Lipid Storage Diseases | Antisocial Personality Disorder | Hereditary Spherocytosis | Nephrotic Syndrome Type 1 | Waardenburg Syndrome Type 1 | Crigler-Najjar Syndrome | Blepharoconjunctivitis | Osteoglophonic Dysplasia | Conjunctivitis, Allergic | Bartsocas-Papas Syndrome