Informaţii despre

Nume Von Hippel-Lindau Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Other phakomatoses, not elsewhere classified
Clasificare anatomică Malacards Boli ale ochiului; Boli cardiovasculare; Boli endocrine; Boli nefrologice (ale rinichilor); Boli neuronale

Vezi şi

Boli A-Z Acute Mountain Sickness Adenocarcinoma Adenoma Adrenal Medulla Cancer Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amenorrhea Aneurysm Angiomatosis Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonia Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autosomal Dominant Polycystic Kidney Disease Autosomal Genetic Disease 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 Branchiootic Syndrome 1 Breast Cancer Breast Papillary Carcinoma Capillary Hemangioma Carcinoid Syndrome Carcinoid Tumors, Intestinal Carney Complex Variant Carney Triad Cerebellar Astrocytoma Cerebritis Cervicitis Chiasmal Syndrome Chondroma Chondrosarcoma Chromosome 3p Deletion Clear Cell Papillary Renal Cell Carcinoma Clear Cell Renal Cell Carcinoma Colon Adenocarcinoma Colorectal Adenocarcinoma Cone-Rod Dystrophy 2 Cowden Disease Cystadenoma Cystic Kidney Disease Delusional Disorder Dilated Cardiomyopathy Duodenal Somatostatinoma Duodenitis Encephalopathy Endocrine Gland Cancer Endolymphatic Sac Tumor Endotheliitis Epithelioid Malignant Peripheral Nerve Sheath Tumor Erythrocytosis, Familial, 2 Extra-Adrenal Pheochromocytoma Familial Renal Papillary Carcinoma Fibrous Meningioma Fumarate Hydratase Deficiency Gallbladder Cancer Gastrinoma Gastrointestinal Neuroendocrine Tumor Gastrointestinal Stromal Tumor Gitelman Syndrome Glioma Glucagonoma Headache Heart Cancer Hemangioblastoma Hemangioma Hepatitis Hereditary Leiomyomatosis and Renal Cell Cancer Hereditary Paraganglioma-Pheochromocytoma Syndromes Hereditary Renal Cell Carcinoma Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperparathyroidism Hyperparathyroidism 2 with Jaw Tumors Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypogonadism Hypoxia Intracranial Aneurysm Intravascular Papillary Endothelial Hyperplasia Islet Cell Tumor Juvenile Hereditary Hemochromatosis Kidney Cancer Leukemia Lung Cancer Lymph Node Disease Macular Holes Malignant Glioma Mediastinitis Meningioma, Familial Meningitis Microcystic Adenoma Mitochondrial Complex Ii Deficiency Multiple Endocrine Neoplasia Multiple Endocrine Neoplasia Type 1 and Type 2 Multiple Endocrine Neoplasia, Type I Multiple Endocrine Neoplasia, Type Iia Multiple Sclerosis Myasthenia Gravis Myelitis Myeloid Leukemia Neural Crest Tumor Neuroendocrine Tumor Neurofibromatosis, Type Iv, of Riccardi Obstructive Hydrocephalus Obstructive Jaundice Optic Nerve Glioma Ovarian Serous Cystadenocarcinoma Pancreatic Cancer Pancreatic Cystadenoma Pancreatic Gastrinoma Pancreatic Islet Cell Tumors Pancreatic Neuroendocrine Tumor Pancreatic Serous Cystadenoma Pancreatitis Papillary Adenoma Paraganglioma Paraganglioma and Gastric Stromal Sarcoma Paragangliomas 1 Paraplegia Parathyroid Adenoma Parathyroid Carcinoma Peritonitis Persistent Generalized Lymphadenopathy Persistent Hyperplastic Primary Vitreous Petrositis Peutz-Jeghers Syndrome Phaeochromocytoma Pharyngitis Pheochromocytoma Pituitary Adenoma Pneumonia Polycystic Kidney Disease Portal Hypertension Primary Hyperparathyroidism Proteus Syndrome Renal Cell Carcinoma, Nonpapillary Renal Clear Cell Carcinoma Retinal Detachment Retinal Hemangioblastoma Retinitis Somatostatinoma Spastic Ataxia, Charlevoix-Saguenay Type Sporadic Pheochromocytoma Sturge-Weber Syndrome Thymoma Thyroid Carcinoma, Familial Medullary Tuberous Sclerosis Weber Syndrome Zollinger-Ellison Syndrome