KCNMA1 Gene and Epilepsy Management disease
Paroxysmal Nonkinesigenic Dyskinesia, 3, with or Without Generalized Epilepsy, also known as generalized epilepsy and paroxysmal dyskinesia, is related to benign familial infantile epilepsy and autosomal dominant nocturnal frontal lobe epilepsy, and has symptoms including absence seizures An important gene associated with Paroxysmal ...
Living with Superficial Spreading Melanoma disease
Superficial Spreading Melanoma, also known as superficial spreading malignant melanoma of skin, is related to melanoma and congenital lipomatous overgrowth, vascular malformations, and epidermal nevi. Affiliated tissues include skin, bone and lymph node.
Kidney Disease Management: Lifestyle and Care disease
Kidney Disease, also known as renal failure, is related to chronic kidney disease and polycystic kidney disease, and has symptoms including polyuria An important gene associated with Kidney Disease is TSC1 (TSC Complex Subunit 1), and among its related pathways/superpathways are Ciliopathies and Bardet-Biedl syndrome. The drugs Amiodarone ...
Cerebrovascular Disease: Risk Factors and Prevention disease
Cerebrovascular Disease, also known as cerebrovascular disorder, is related to basal ganglia cerebrovascular disease and stroke, ischemic, and has symptoms including headache, transient ischemic attacks, stereotypic symptoms and angina pectoris. An important gene associated with Cerebrovascular Disease is HOTAIR (HOX Transcript Antisense ...
Elevating Your Aarskog-Scott Syndrome Care disease
Aarskog-Scott Syndrome, also known as aarskog syndrome, is related to unilateral focal polymicrogyria and aarskog syndrome, autosomal dominant. An important gene associated with Aarskog-Scott Syndrome is FGD1 (FYVE, RhoGEF And PH Domain Containing 1), and among its related pathways/superpathways are Signal Transduction and GPCR downstream ...