Asphyxia Neonatorum

About the Disease
Asphyxia Neonatorum, also known as postnatal asphyxia, is related to neonatal hypoxic and ischemic brain injury and newborn respiratory distress syndrome. An important gene associated with Asphyxia Neonatorum is COL1A1 (Collagen Type I Alpha 1 Chain), and among its related pathways/superpathways are Signal Transduction and PI3K-Akt signaling pathway. The drugs Tocopherol and Sertraline have been mentioned in the context of this disorder. Affiliated tissues include brain, heart and liver, and related phenotypes are no effect and no effect

Common Targets
ACE | NOS1 | G7124 | SMPD4 | CIRBP | XDH | MTHFR | NTSR1 | NOS2 | TH | GSTP1 | AGTR1 | NLRP3 Inflammasome | G114548

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

Other Diseases

Malaria | VACTERL Association | Amish Infantile Epilepsy Syndrome | Chediak-Higashi Syndrome | Acne | Esotropia | Neurofibroma, Plexiform | Thrombophilia | Cannabis Abuse | Keratocystic Odontogenic Tumor | Glioblastoma Multiforme | Dysthymia | Large Granular Lymphocytic Leukemia | Juvenile Hyaline Fibromatosis | Myhre Syndrome | Hypotrichosis Simplex | Nicotine Dependence | Hyper IgE Syndrome | Primary Erythromelalgia | Leukoplakia, Oral | Schnitzler Syndrome | Pyruvate Decarboxylase Deficiency | Angelman Syndrome | Panic Disorder | Schaaf-Yang Syndrome | Lymphedema | Insulin Resistance | Erythrokeratodermia Variabilis | Raine Syndrome | Hyperphenylalaninemia | Mycosis Fungoides | Thalassemia | Astigmatism | Joubert Syndrome | Erdheim-Chester Disease | Cholangitis | Adrenal Insufficiency | Marinesco-Sjogren Syndrome | Osteosarcoma | Acute Myeloid Leukemia | Leri Pleonosteosis | Familial Dysautonomia | Focal Segmental Glomerulosclerosis | Hemorrhoids | Nephritis, Interstitial | Blepharo-cheilo-odontic Syndrome | Glycogen Storage Disease | Anovulation | Scabies | Phenylketonuria | Dwarfism | Plasma Cell Leukemia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Microvillus Inclusion Disease | Mixed Connective Tissue Disease | Neurocysticercosis | Persistent Mullerian Duct Syndrome | Epidermolysis Bullosa Simplex, Localized | Familial Episodic Pain Syndrome | Anorexia Nervosa | Aarskog-Scott Syndrome | Aceruloplasminemia | Neuromyelitis Optica | Restrictive Dermopathy | Cutaneous Mastocytosis | Dermatofibrosarcoma | Cancer, Skin | Episodic Ataxia Type 2 | Sepiapterin Reductase Deficiency | Granular Corneal Dystrophy | Pierson Syndrome | Neurodevelopmental Disorders | Uveitis | Loeys-Dietz Syndrome | Primary Biliary Cholangitis | TARP Syndrome | Mast Cell Leukemia | Sclerocornea | Esthesioneuroblastoma | Presbycusis | Empyema | Dysequilibrium Syndrome | Porokeratosis | Spasticity | Syncope | Alcoholism | Migraine | Learning Disability | Cardiac Sarcoidosis | Long QT Syndrome Type 3 | Alexander Disease | Parkinson Disease 6, Autosomal Recessive Early-onset | Glutaric Aciduria Type 2 | Sclerosteosis | Chronic Inflammatory Demyelinating Polyneuropathy | Carcinoma, Merkel Cell | Precocious Puberty | C3 Glomerulonephritis | Hyperthermia, Malignant | Spinocerebellar Ataxia Type 15 | Epidermolytic Palmoplantar Keratoderma | Ataxia-ocular Apraxia 2 | Parkinsonism | Charcot-Marie-Tooth Disease Type 2E | Tylosis With Esophageal Cancer | Ectodermal Dysplasia | Lipid Metabolism Disorders | Cantu Syndrome | Schizencephaly | Tuberculosis | Androgenic Alopecia | Acne Vulgaris | Non-Hodgkin Lymphoma | Thromboembolism | Congenital Myasthenic Syndrome | Melanoma, Malignant | Fetal Akinesia Deformation Sequence | Oculopharyngeal Muscular Dystrophy | Paget's Disease Of The Breast | Glomerulonephritis | Lesch-Nyhan Syndrome | Dubin-Johnson Syndrome | Sporadic Inclusion Body Myositis | Tyrosinemia | Gastritis, Atrophic | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Cleidocranial Dysplasia | Thymoma, Malignant | Generalized Epilepsy And Paroxysmal Dyskinesia | Fabry's Disease | Language Disorders | Paraganglioma, Carotid Body | Atopy | Persistent Truncus Arteriosus | Varices | Trichuriasis | Celiac Disease | Moyamoya Disease | Phosphoglycerate Dehydrogenase Deficiency | Goiter | Amyotrophic Lateral Sclerosis | Nemaline Myopathy | Acrocallosal Syndrome | Skin Fragility-woolly Hair Syndrome | Becker Muscular Dystrophy | Gastric Atrophy | Binge Eating Disorder | Familial Partial Lipodystrophy | Dent Disease | Carney Triad | Dermatomyositis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Werner's Syndrome | Acute Tubular Necrosis | Lennox-Gastaut Syndrome | Noonan Syndrome | IgA Deficiency | Hypercalciuria | Connective Tissue Disorders | Neurodermatitis | Stuve-Wiedemann Syndrome | Multiple Epiphyseal Dysplasia | Retinitis Pigmentosa 3 | Familial Mediterranean Fever | Bulimia Nervosa | Heterotopic Ossification | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Tetraplegia | Spondylo-ocular Syndrome | Keratoacanthoma | Vulvovaginitis | Gynecomastia | Craniometaphyseal Dysplasia | Cancer, Lung | Mumps | Polycystic Kidney, Autosomal Dominant | Cellulitis | Membranous Nephropathy | Homocystinuria | Cat Eye Syndrome | Rhinitis | Diabetic Encephalopathy | Chondromyxoid Fibroma | Cystinosis | Rubeosis Iridis | Hepatoblastoma | Oculodentodigital Dysplasia | COACH Syndrome | Hereditary Sensory And Autonomic Neuropathy | Carcinoma, Squamous Cell | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Agranulocytosis | Mevalonate Kinase Deficiency | Encephalitis, Tick-borne | Thrombosis | Acute Chest Syndrome | Tardive Dyskinesia | Retinitis Pigmentosa | Hypopigmentation | Juvenile Xanthogranuloma | Encephalocele | Pneumoconiosis | Impetigo | Filariasis | Gout | Sarcoma, Alveolar Soft Part | Peripheral T-cell Lymphoma | Mucolipidosis | Mucolipidosis Type III | Renal Medullary Carcinoma | Infectious Diarrhea | Viral Meningitis | Erythema Nodosum | Short-chain Acyl-CoA Dehydrogenase Deficiency | Autosomal Recessive Congenital Ichthyosis | Proteasome-associated Autoinflammatory Syndrome 2 | Meningioma | VEXAS Syndrome | Bartter Syndrome | Gastroenteritis, Eosinophilic | Epidermolysis Bullosa Dystrophica | Basal Ganglia Cerebrovascular Disease | Antiphospholipid Syndrome | Poretti-Boltshauser Syndrome | Rolandic Epilepsy | Peeling Skin Syndrome Type B | Congenital Muscular Dystrophy | N-acetylglutamate Synthase Deficiency | Japanese Encephalitis | Early Infantile Epileptic Encephalopathy 4 | Barakat Syndrome | B-cell Prolymphocytic Leukemia | Congenital Sodium Diarrhea | Iron Overload | Adenomatoid Tumor | Rhabdoid Tumor | VACTERL/VATER Association | Fibrosarcoma | Blepharitis | Multiple Sclerosis, Secondary Progressive | Temporal Lobe Epilepsy | Benign Familial Neonatal Convulsions | Myeloid Leukemia | Congenital Generalized Lipodystrophy | Ventricular Septal Defect | Ocular Hypertension | Ollier Disease | Rhabdomyosarcoma, Alveolar | Spinocerebellar Ataxia Type 3 | Norrie Disease | Geleophysic Dysplasia | Adenosine Deaminase Deficiency | Adenylosuccinate Lyase Deficiency | Rift Valley Fever | Leukocyte Adhesion Deficiency | Hepatorenal Syndrome | Oligodendroglioma | Thyroiditis | Progressive Familial Intrahepatic Cholestasis Type 1 | Macrophagic Myofasciitis | Congenital Dyserythropoietic Anemia Type 1 | Hodgkin Lymphoma | Peeling Skin Syndrome, Acral Type | Dyslexia | Duchenne Muscular Dystrophy | Dengue Shock Syndrome | Carcinoma In Situ | Zellweger Syndrome | Seborrheic Dermatitis | Glycogen Storage Disease Type 5 | Relapsing Polychondritis | Hepatopulmonary Syndrome | Hypogammaglobulinemia | Angiodysplasia | Pycnodysostosis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Hypothyroidism | Carney-Stratakis Syndrome | Hereditary Inclusion Body Myopathy | Pancreatitis | Chudley-McCullough Syndrome | Klinefelter Syndrome | Wolff-Parkinson-White Syndrome | Inflammatory Bowel Disease | Neonatal Progeroid Syndrome | Mastitis | GM2-gangliosidosis AB Variant | Eczema | Antenatal Bartter Syndrome Type 1 | Tangier Disease | Tricho-hepato-enteric Syndrome | Antisocial Personality Disorder | Double Outlet Right Ventricle | Cervical Dystonia | Bietti Crystalline Dystrophy | Partington Syndrome | Avellino Corneal Dystrophy | Hemimegalencephaly | IgA Nephropathy | Combined Pituitary Hormone Deficiency | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Speech Disorders | Renal Tubular Dysgenesis | Pneumococcal Meningitis | Pyruvate Dehydrogenase Deficiency | Waardenburg Syndrome Type 4A | Protein S Deficiency | Veno-occlusive Disease | Epidermolysis Bullosa Simplex | Hereditary Folate Malabsorption | Branchiootorenal Syndrome | Diabetes Mellitus, Transient Neonatal | Otopalatodigital Syndrome Type 2 | Panniculitis | Hemosiderosis | Glioma | Facioscapulohumeral Muscular Dystrophy | Hydronephrosis | Eclampsia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Feingold Syndrome | DEND Syndrome | Stuttering | Dowling-Degos Disease | Cystitis | Asthma | Optic Neuropathy, Anterior Ischemic | Trachoma | Nicotine Addiction | Narcolepsy | Charcot-Marie-Tooth Disease Type 4B1 | Sezary Syndrome | Tendinitis | Poirier-Bienvenu Neurodevelopmental Syndrome | Myositis | Polycythemia | Craniofrontonasal Syndrome | Neuroblastoma | Amyotrophic Lateral Sclerosis, Juvenile | Sialoadenitis | Encephalopathy, Ethylmalonic | Jaundice, Obstructive | LRBA Deficiency | Peutz-Jeghers Syndrome | Tatton-Brown-Rahman Syndrome | Hypoalbuminemia | Astrocytoma, Anaplastic | Hernia, Inguinal | Spinocerebellar Ataxia Type 28 | Methemoglobinemia Type IV | Cirrhosis | Tuberculous Meningitis | Myasthenia Gravis | X-linked Creatine Transporter Deficiency | Pulmonary Alveolar Microlithiasis | Nephrotic Syndrome Type 1 | Preaxial Polydactyly | Chronic Granulomatous Disease | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Malignant Peripheral Nerve Sheath Tumor | 3-methylglutaconic Aciduria | Distal Spinal Muscular Atrophy | Hypertension, Pulmonary | Atherosclerosis | Pemphigus | Takayasu's Arteritis | Open-angle Glaucoma | Giant Cell Arteritis | Crigler-Najjar Syndrome | Neuronal Ceroid Lipofuscinosis | Hyperinsulinemia | Osteoarthritis | Sarcoma, Endometrial Stromal | Benign Recurrent Intrahepatic Cholestasis 1 | Retinal Detachment | Deafness, Dystonia, And Cerebral Hypomyelination | Fetal Alcohol Syndrome | Cousin Syndrome | Eiken Syndrome | Blood Protein Disorders | Hyperkalemic Periodic Paralysis | Silver-Russell Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Sarcoidosis | Purpura | Melanocytic Nevus | Auriculocondylar Syndrome | Alveolar Capillary Dysplasia | Carcinoid Syndrome | Cryptosporidiosis | Schwannoma | Apert Syndrome | 3-methylglutaconic Aciduria Type I | Epidermolysis Bullosa Acquisita | Placenta Previa | Colitis | Krabbe Disease | Ichthyosis Bullosa Of Siemens | H Syndrome | Hypolipoproteinemia