Elevating Your Liddle Syndrome Lifestyle disease
Liddle Syndrome 1, also known as liddle syndrome, is related to hypertension, essential and hypokalemia. An important gene associated with Liddle Syndrome 1 is SCNN1B (Sodium Channel Epithelial 1 Subunit Beta), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Neuropathic ...
Easing Exfoliative Dermatitis: Gentle Care Tips disease
Exfoliative Dermatitis is related to holocarboxylase synthetase deficiency and dermatitis, and has symptoms including exanthema An important gene associated with Exfoliative Dermatitis is SPINK5 (Serine Peptidase Inhibitor Kazal Type 5). Affiliated tissues include skin, liver and bone marrow.
Understanding Hemosiderosis: Genetic Iron Overload disease
Rare Hereditary Hemochromatosis, also known as iron overload, is related to hemochromatosis, type 5 and iron overload in africa. An important gene associated with Rare Hereditary Hemochromatosis is HFE (Homeostatic Iron Regulator), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino ...
Eosinophilic Pneumonia: Symptoms, Lifestyle, and Management disease
Eosinophilic Pneumonia, also known as asthmatic pulmonary eosinophilia, is related to t2-high asthma and chronic eosinophilic pneumonia, and has symptoms including hemoptysis and coughing. An important gene associated with Eosinophilic Pneumonia is IL5 (Interleukin 5), and among its related pathways/superpathways are Innate Immune System and ...
Understanding Autosomal Dominant Polycystic Kidney Disease disease
Autosomal Dominant Polycystic Kidney Disease, also known as polycystic kidney disease, adult type, is related to polycystic kidney disease and polycystic kidney disease 1 with or without polycystic liver disease. An important gene associated with Autosomal Dominant Polycystic Kidney Disease is PKD1 (Polycystin 1, Transient Receptor Potential ...