Understanding Osteogenesis Imperfecta Type V disease
Osteogenesis Imperfecta, Type V, also known as osteogenesis imperfecta type 5, is related to osteogenesis imperfecta, type vi and brittle bone disorder. An important gene associated with Osteogenesis Imperfecta, Type V is IFITM5 (Interferon Induced Transmembrane Protein 5), and among its related pathways/superpathways are Binding and Uptake ...
Living with PDA: Tips for Management disease
Patent Ductus Arteriosus 1, also known as patent ductus arteriosus, is related to aortic aneurysm, familial thoracic 4 and holt-oram syndrome. An important gene associated with Patent Ductus Arteriosus 1 is FLNA (Filamin A), and among its related pathways/superpathways are Cardiac conduction and Human Embryonic Stem Cell Pluripotency. The ...
Arteriosclerosis: Preventive Measures and Lifestyle disease
Arteriosclerosis, also known as arteriosclerotic vascular disease, is related to arteriosclerosis obliterans and aortic atherosclerosis, and has symptoms including angina pectoris An important gene associated with Arteriosclerosis is HS3ST1 (Heparan Sulfate-Glucosamine 3-Sulfotransferase 1), and among its related pathways/superpathways are ...
Understanding Reflex Epilepsy: Symptoms and Care disease
Reflex Epilepsy, also known as epilepsy, reflex, is related to photosensitive epilepsy and episodic kinesigenic dyskinesia 1. An important gene associated with Reflex Epilepsy is SCNM1 (Sodium Channel Modifier 1), and among its related pathways/superpathways are Transmission across Chemical Synapses and Neuroscience. The drugs Valproic acid ...
Gaze Palsy: Managing Symptoms and Lifestyle disease
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 2, with Impaired Intellectual Development, also known as gaze palsy, familial horizontal, with progressive scoliosis, 2, is related to mirror movements 1 and corpus callosum, agenesis of. An important gene associated with Gaze Palsy, Familial Horizontal, with Progressive Scoliosis ...