Informaţii despre

Nume Adrenocortical Carcinoma, Hereditary
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Malignant neoplasm: Cortex of adrenal gland
Clasificare anatomică Malacards Boli ale sistemului reproducator; Boli cardiovasculare; Boli endocrine; Boli nefrologice (ale rinichilor)

Vezi şi

Boli A-Z 46,xx Sex Reversal 1 46 Xy Gonadal Dysgenesis Acute Adrenal Insufficiency Adenocarcinoma Adenoma Adie Pupil Adrenal Adenoma Adrenal Carcinoma Adrenal Cortex Disease Adrenal Cortical Adenoma Adrenal Cortical Hypofunction Adrenal Gland Disease Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Adrenal Hypoplasia, Congenital Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete Adrenal Rest Tumor Adrenocortical Carcinoma with Pure Aldosterone Hypersecretion Aging Aldosterone-Producing Adenoma Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Antley-Bixler Syndrome Aplasia Cutis Congenita Aplasia Cutis Congenita, Nonsyndromic Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia Beckwith-Wiedemann Syndrome Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bornholm Eye Disease Carpal Tunnel Syndrome Cellular Ependymoma Central Nervous System Primitive Neuroectodermal Neoplasm Cerebellum Cancer Cerebral Neuroblastoma Cerebral Ventricle Cancer Cerebritis Cerebrum Cancer Choriocarcinoma Choroiditis Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conn's Syndrome Corpus Callosum, Agenesis of Cytochrome P450 Oxidoreductase Deficiency Diphtheria Dowling-Degos Disease 1 Endotheliitis Familial Glucocorticoid Deficiency Familial Hyperaldosteronism Ganglioneuroblastoma Ganglioneuroma Gastrointestinal Stromal Tumor Genitopatellar Syndrome Gestational Trophoblastic Neoplasm Glomus Tumor Gynecomastia Hemihyperplasia, Isolated Hepatic Adenomas, Familial Hepatitis Hepatocellular Carcinoma Horseshoe Kidney Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoadrenocorticism, Familial Hypoglycemia Hypokalemia Hypopituitarism Immunodeficiency, Common Variable, 10 Infant Gynecomastia Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Kaposi Sarcoma Leiomyomatosis Leydig Cell Tumor Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Lipoid Congenital Adrenal Hyperplasia Liposarcoma Lung Cancer Luteoma Lymphoma Lynch Syndrome Mantle Cell Lymphoma Meninges Sarcoma Multiple Endocrine Neoplasia Myopathy, Distal, with Anterior Tibial Onset Myxosarcoma Neuroblastoma Neuroendocrine Tumor Neuronitis Organ System Benign Neoplasm Papillary Thyroid Microcarcinoma Papilloma of Choroid Plexus Papillomatosis, Confluent and Reticulated Paraganglioma Periodontitis, Aggressive, 1 Peritonitis Persistent Idiopathic Facial Pain Peutz-Jeghers Syndrome Pheochromocytoma Pleomorphic Xanthoastrocytoma Polycystic Ovary Syndrome Precocious Puberty Premature Ovarian Failure 1 Prostatitis Pseudohermaphroditism Pyle Disease Retinoblastoma Retroperitoneal Liposarcoma Rhabdomyosarcoma Sarcoma Seminoma Sertoli Cell Tumor Sex Cord-Gonadal Stromal Tumor Sex Differentiation Disease Silver-Russell Syndrome Due to a Point Mutation Spastic Paraplegia 17, Autosomal Dominant Squamous Cell Carcinoma Steroid Inherited Metabolic Disorder Teratoma Testicular Leydig Cell Tumor Testicular Seminoma Thrombosis Thyroid Cancer Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Transsexualism Turner Syndrome Umbilical Hernia Uterine Corpus Endometrial Carcinoma Varicocele Wilms Tumor 1