Informaţii despre

Nume Apparent Mineralocorticoid Excess
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Secondary hyperaldosteronism
Clasificare anatomică Malacards Boli cardiovasculare; Boli endocrine; Boli nefrologice (ale rinichilor)

Vezi şi

Boli A-Z Ablepharon-Macrostomia Syndrome Acth-Secreting Pituitary Adenoma Acute Adrenal Insufficiency Acute Thyroiditis Adie Pupil Adrenal Adenoma Adrenal Cortex Disease Adrenal Cortical Hypofunction Adrenal Gland Disease Adrenal Gland Hyperfunction Adult Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Anuria Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 3 Bartter Disease Bartter Syndrome, Type 3 Blood Group--Ahonen Blood Group, I System Conn's Syndrome Corticosteroid-Binding Globulin Deficiency Cystic Fibrosis Diabetes Insipidus Endocrine Organ Benign Neoplasm Familial Glucocorticoid Deficiency Familial Hypertension Gitelman Syndrome Hemangioma-Thrombocytopenia Syndrome Hepatic Adenomas, Familial Hyperaldosteronism, Familial, Type I Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hypoaldosteronism Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypokalemia Inappropriate Adh Syndrome Juvenile Hereditary Hemochromatosis Kabuki Syndrome 1 Liddle Syndrome Mineral Metabolism Disease Musical Perfect Pitch Nelson Syndrome Nephrocalcinosis Ocular Hypertension Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Pseudohypoaldosteronism Pseudohypoaldosteronism, Type I, Autosomal Dominant Pseudohypoaldosteronism, Type I, Autosomal Recessive Renal Tubular Acidosis Renal Tubular Transport Disease Retinitis Steroid Inherited Metabolic Disorder Suprasellar Meningioma Testicular Leydig Cell Tumor Trichinosis