Disease

Fetal And Neonatal Alloimmune Thrombocytopenia

About the Disease
Fetal and Neonatal Alloimmune Thrombocytopenia, also known as neonatal alloimmune thrombocytopenia, is related to thrombocytopenia and thrombocytopenia due to platelet alloimmunization. An important gene associated with Fetal and Neonatal Alloimmune Thrombocytopenia is CD109 (CD109 Molecule), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and PI3K-Akt signaling pathway. The drugs gamma-Globulins and Rho(D) Immune Globulin have been mentioned in the context of this disorder. Affiliated tissues include brain, skin and whole blood, and related phenotypes are neonatal alloimmune thrombocytopenia and petechiae

Common Targets
CD36 | ITGB3

疾病靶点研报
Fetal And Neonatal Alloimmune Thrombocytopenia

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

Other Diseases

Amyotrophic Lateral Sclerosis, Juvenile | Imerslund-Grasbeck Syndrome | Dubin-Johnson Syndrome | Goiter | Alpha-mannosidosis | Norrie Disease | Schizotypal Personality Disorder | Schamberg Disease | Hypobetalipoproteinemias | Vulvovaginitis | Cornelia De Lange Syndrome | Thrombophilia | Paroxysmal Kinesigenic Dyskinesia | Adenomatoid Tumor | Vascular Cognitive Impairment | Porphyria Cutanea Tarda | X-linked Acrogigantism | Mood Disorder | Hypervalinemia | Exocrine Pancreatic Insufficiency | Hereditary Coproporphyria | Leukocyte Adhesion Deficiency Type 1 | Eccrine Porocarcinoma | Jacobsen Syndrome | Motor Neuron Diseases | Infantile Nephropathic Cystinosis | Gangliosidosis, GM1 | Sclerosing Cholangitis | Primary Hyperoxaluria | Hypermetropia | Angioimmunoblastic T-cell Lymphoma | Liver Failure | Abetalipoproteinemia | Pigment Dispersion Syndrome | Angioedema, Acquired | Bullous Pemphigoid | Intracerebral Hemorrhage | Congenital Dysfibrinogenemia | Acute Tubular Necrosis | Disseminated Intravascular Coagulation | Distal Spinal Muscular Atrophy | Chondrodysplasia Punctata 1, X-linked Recessive | Schizencephaly | Macular Degeneration | Hypoplastic Left Heart Syndrome | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Hypertension, Renovascular | Pontocerebellar Hypoplasia Type 7 | Hepatic Steatosis | Familial Hypertrophic Cardiomyopathy | Osteopetrosis | Birk-Barel Syndrome | Arthrogryposis | Hyperandrogenemia | Atelosteogenesis Type 1 | Thalassemia | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Glomerulonephritis, Membranoproliferative | Measles | Fabry's Disease | Atrioventricular Septal Defect | Uveitis, Anterior | Epidermolysis Bullosa Dystrophica | Neural Tube Defect | Thyrotoxic Periodic Paralysis | Glioma | Renal Hypomagnesemia 3 | Macrodactyly | Bainbridge-Ropers Syndrome | Tyrosinemia | Retinitis Pigmentosa | Cardiomyopathy, Peripartum | Hyperbilirubinemia | Smoldering Myeloma | Primary Carnitine Deficiency | Familial Male-limited Precocious Puberty | Congenital Diaphragmatic Hernia | Parkinsonism | Myofibrillar Myopathy | Lymphoma | Lymphedema-distichiasis Syndrome | L-2-Hydroxyglutaric Aciduria | Mastitis | Dystonia-parkinsonism, X-linked | Stiff-man Syndrome | Teratozoospermia | Lymphangiomatosis | Esthesioneuroblastoma | Pseudohermaphroditism | Urethritis | Hyperacusis | Congenital Disorders Of Glycosylation Type II | Neurodevelopmental Disorders | Subacute Sclerosing Panencephalitis | Blepharo-cheilo-odontic Syndrome | Acral Lentiginous Melanoma | Tic Disorder | Aspartylglycosaminuria | Kernicterus | Sclerosteosis | Cardiomyopathy, Restrictive | Rash | Intestinal Hypomagnesemia 1 | Joubert Syndrome | Atopy | Optic Neuritis | Anxiety Disorders | Spinocerebellar Ataxia Type 8 | Veno-occlusive Disease | Glutathione Synthetase Deficiency | Lymphopenia | Peripheral Neuropathy | Supravalvular Aortic Stenosis | Diabetic Neuropathy | Amelanotic Melanoma | Rotor Syndrome | Carbamoyl Phosphate Synthetase I Deficiency | Meningococcal Meningitis | Klippel-Feil Syndrome | Hartnup Disease | Vertebrobasilar Insufficiency | Maternally Inherited Diabetes And Deafness | Osteopathia Striata With Cranial Sclerosis | Facioscapulohumeral Muscular Dystrophy | Hemosiderosis | Blepharospasm | Spina Bifida | Oculocutaneous Albinism Type 4 | Tendinitis | Glycogen Storage Disease Type 6 | Raine Syndrome | Hypocalcemia | Idiopathic Multicentric Castleman Disease | Jalili Syndrome | Alopecia Areata | Usher Syndrome Type II | Chronic Granulomatous Disease, X-linked | Mesothelioma, Malignant | Neurodegeneration With Brain Iron Accumulation | Ectrodactyly | Congenital Central Hypoventilation Syndrome | Chromosome 9q34.3 Deletion Syndrome | Early Infantile Epileptic Encephalopathy 4 | AIDS | Toxoplasmosis | Familial Isolated Hyperparathyroidism | Marfan Syndrome | Hemorrhoids | Charcot-Marie-Tooth Disease, Type 2C | Glanzmann Thrombasthenia | Gangliosidosis | Haim-Munk Syndrome | Familial Hemiplegic Migraine | Hemolytic Anemia | Angiomyolipoma | X-linked Sideroblastic Anemia | Takayasu's Arteritis | Keratopathy | Prolactinoma | Sarcoma, Alveolar Soft Part | Erythema Multiforme | Recurrent Respiratory Papillomatosis | Ischemia | Fraser Syndrome | Heart Failure | Periventricular Nodular Heterotopia | Prolymphocytic Leukemia | Pseudohypoparathyroidism Type 1A | Hyperthermia, Malignant | Chronic Enteropathy Associated With SLCO2A1 Gene | Polymicrogyria | Ectopia Lentis, Isolated, Autosomal Recessive | Gallstones | Lipid Storage Diseases | Nephrotic Syndrome | Leiomyoma | Acquired Partial Lipodystrophy | Leri-Weill Dyschondrosteosis | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Hyperostosis | Gyrate Atrophy Of The Choroid And Retina | Congenital Aniridia | Inflammatory Myofibroblastic Tumor | Spinal And Bulbar Muscular Atrophy | Leukodystrophies | Hyperuricemia | Pneumoconiosis | Aceruloplasminemia | Neurocysticercosis | Osteochondroma | Oculocutaneous Albinism | Spasticity | Presbyopia | Obesity | Anuria | Apert Syndrome | Tyrosinemia Type 2 | Gilbert Syndrome | Juvenile Hyaline Fibromatosis | Hyperparathyroidism | Panic Disorder | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Non-Langerhans Cell Histiocytosis | Lentigo | Exotropia | Bone Marrow Necrosis | Vitreoretinal Degeneration, Snowflake Type | Iron Overload | Cabezas Syndrome | Aldosteronism | Combined Deficiency Of Factor V And Factor VIII | Meleda Disease | Sialoadenitis | Aplasia Cutis Congenita | Sleep Apnea, Central | Hemangioblastoma | Congenital Heart Block | Myhre Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Alkaptonuria | Dysmorphophobia | Hemolytic Uremic Syndrome, Atypical | Echinococcosis | Gardner Syndrome | NDH Syndrome | Treacher Collins Syndrome | Cholesteryl Ester Storage Disease | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Facioscapulohumeral Muscular Dystrophy Type 1 | Down Syndrome | Proteus Syndrome | Adenomyosis | Cryptosporidiosis | Nijmegen Breakage Syndrome | Sturge-Weber Syndrome | Nail-Patella Syndrome | Photosensitivity | Mannosidase Deficiency Diseases | Spinocerebellar Ataxia Type 16 | Iron Deficiency Anemia | Megalencephaly | Persistent Truncus Arteriosus | Presbycusis | Rhabdomyosarcoma, Embryonal | Myositis | Hemochromatosis Type 1 | Hemochromatosis | Heart Block | Glycogen Storage Disease | Neuropathy | Corneal Dystrophies, Hereditary | Personality Disorders | Van Der Knaap Disease | Sarcoma, Endometrial Stromal | Gestational Trophoblastic Disease | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Corneal Ulcer | Otosclerosis | Arthropathy | Lipoma | Lamellar Ichthyosis | Ataxia-ocular Apraxia 2 | Adenoma, Pleomorphic | Ureteropelvic Junction Obstruction | Ganglioglioma | Esotropia | Vogt-Koyanagi-Harada Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Arts Syndrome | Glycogen Storage Disease Type 3 | Mycosis Fungoides | Hypereosinophilic Syndrome | Learning Disability | Dental Caries | Cluster Headache | Ocular Albinism Type 1 | Pilomatrix Carcinoma | Yellow Fever | Gaucher Disease | Postpoliomyelitis Syndrome | Cystinosis | Antenatal Bartter Syndrome Type 1 | Nevus | Botulism | Pseudoexfoliation Syndrome | Dysferlinopathy | Proopiomelanocortin Deficiency | Loeys-Dietz Syndrome | Keratocystic Odontogenic Tumor | Adrenomyeloneuropathy | Cryoglobulinemia | Guanidinoacetate Methyltransferase Deficiency | Pituitary Dwarfism | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Bardet-Biedl Syndrome | Retinitis | Perry Syndrome | GM2-gangliosidosis AB Variant | Shock, Cardiogenic | Metaphyseal Chondrodysplasia, Schmid Type | Psoriasis | Pyloric Stenosis, Infantile Hypertrophic | Hemangioma | Impulse Control Disorder | Methylmalonic Acidemia | Gastroschisis | Amenorrhea | Cyclic Vomiting Syndrome | Cardiomyopathy, Hypertrophic | Pancreatitis, Chronic | Pulverulent Zonular Cataract | Stuttering | Pulmonary Alveolar Proteinosis | Gnathodiaphyseal Dysplasia | Early Infantile Epileptic Encephalopathy 13 | Hypertensive Retinopathy | IgA Deficiency | Dent Disease | Crohn's Disease | Majeed Syndrome | Congenital Poikiloderma | Papulopustular Rosacea | Erythromelalgia | Pyelonephritis | Hartsfield Syndrome | Hydrocephalus, Normal Pressure | Colitis, Lymphocytic | Fibronectin Glomerulopathy | Nephrosclerosis | Chylomicron Retention Disease | Autoimmune Polyendocrine Syndrome | Primary Ovarian Insufficiency | Spinal Muscular Atrophy | Chondrosarcoma | Epicondylitis | Scleroderma, Diffuse | Gynecomastia | Marshall-Smith Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Schwannomatosis | Charcot-Marie-Tooth Disease, Type 6 | Congenital Disorders Of Glycosylation | Carpenter Syndrome | Zellweger Syndrome | Cataract | Waldenstrom Macroglobulinemia | Carcinoma, Transitional Cell | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Ovarian Sex Cord-stromal Tumor | Hydrocephalus | Kindler Syndrome | Tenosynovial Giant Cell Tumor | Ophthalmoplegia | Chondroma | Thyroid Dysgenesis | Cranioectodermal Dysplasia | Papilledema | Myelitis | Gitelman Syndrome | Neutrophilia | DEND Syndrome | Hemorrhagic Disorders | T-cell Chronic Lymphocytic Leukemia | Primary Sclerosing Cholangitis | Low Tension Glaucoma | Pyoderma Gangrenosum | Polyomavirus Nephropathy | Bipolar Disorder | T-cell Lymphoma, Subcutaneous Panniculitis-like | Nemaline Myopathy 8 | Peyronie's Disease | Panuveitis | Fibromyalgia | Multiple Myeloma | Fascioliasis | Peripheral T-cell Lymphoma | Costello Syndrome | Cardiospondylocarpofacial Syndrome | DICER1 Syndrome | Dengue Shock Syndrome | Anosmia, Congenital | Danon Disease | Pseudohypoparathyroidism Type 1C | Polycythemia | Hypokalemic Periodic Paralysis | Autosomal Recessive Spastic Paraplegia Type 35 | Rubeosis Iridis | Ectodermal Dysplasia | Metabolic Syndrome | Trimethylaminuria | Sialidosis | 3-methylglutaconic Aciduria Type I | Familial Dysautonomia | Open-angle Glaucoma | Aneurysm, Thoracic Aortic | Hepatitis, Alcoholic | Olmsted Syndrome | Spinocerebellar Ataxia Type 5