Informaţii despre

Nume Adrenal Adenoma
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare; Bolile canceroase
Clasificare anatomică Malacards Boli endocrine

Vezi şi

Boli A-Z Achalasia-Addisonianism-Alacrima Syndrome Acromegaly Acth Deficiency, Isolated Acth-Secreting Pituitary Adenoma Acute Adrenal Insufficiency Adenocarcinoma Adenoma Adrenal Carcinoma Adrenal Cortex Disease Adrenal Cortical Adenoma Adrenal Cortical Hypofunction Adrenal Gland Disease Adrenal Gland Hyperfunction Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete Adrenal Rest Tumor Adrenocortical Carcinoma, Hereditary Aging Aldosterone-Producing Adenoma Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amenorrhea Aneurysm Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Antley-Bixler Syndrome Apparent Mineralocorticoid Excess Arthritis Arthrochalasia Ehlers-Danlos Syndrome Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia Autosomal Dominant Polycystic Kidney Disease Beckwith-Wiedemann Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Breast Cancer Carney Complex Variant Cell Type Benign Neoplasm Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Clear Cell Renal Cell Carcinoma Conn's Syndrome Cortisone Reductase Deficiency Cytochrome P450 Oxidoreductase Deficiency Diabetes Insipidus Ectopic Cushing Syndrome Empty Sella Syndrome Encephalopathy Endocrine Organ Benign Neoplasm Endotheliitis Familial Adenomatous Polyposis Familial Glucocorticoid Deficiency Familial Hyperaldosteronism Fatty Liver Disease Fibromuscular Dysplasia Gardner-Diamond Syndrome Glucocorticoid Deficiency 1 Gynecomastia Hepatic Adenomas, Familial Hepatocellular Carcinoma Hyperaldosteronism, Familial, Type I Hyperandrogenism Hyperparathyroidism Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypoadrenalism Hypoadrenocorticism, Familial Hypoaldosteronism Hypokalemia Hypothalamic Disease Inappropriate Adh Syndrome Infant Gynecomastia Intracranial Hypertension Kidney Cancer Leydig Cell Tumor Lipoid Congenital Adrenal Hyperplasia Liver Disease Lung Cancer Lupus Erythematosus Malignant Hypertension Medullary Sponge Kidney Multiple Endocrine Neoplasia Multiple Endocrine Neoplasia, Type I Myasthenia Gravis Myopathy Myxosarcoma Nelson Syndrome Olivopontocerebellar Atrophy Open-Angle Glaucoma Organ System Benign Neoplasm Paraneoplastic Syndromes Pemphigus Pemphigus Foliaceus Peritonitis Pheochromocytoma Pituitary Adenoma Pituitary Carcinoma Pituitary-Dependent Cushing's Disease Pituitary Gland Disease Polycystic Kidney Disease Polycystic Ovary Syndrome Precocious Puberty Premenstrual Tension Prostatitis Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Renovascular Hypertension Rheumatoid Arthritis Sertoli-Leydig Cell Tumor Sex Differentiation Disease Sheehan Syndrome Sleep Apnea Steroid Inherited Metabolic Disorder Suprasellar Meningioma Systemic Lupus Erythematosus Testicular Leydig Cell Tumor Thyroiditis Thyrotoxic Periodic Paralysis Transsexualism