Informaţii despre

Nume Tuberous Sclerosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Tuberous sclerosis
Clasificare anatomică Malacards Boli ale ochiului; Boli de piele; Boli nefrologice (ale rinichilor); Boli neuronale
Boli din aceeaşi familie Tuberous Sclerosis 1; Tuberous Sclerosis 2

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Boli A-Z Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion Acute Pancreatitis Adenocarcinoma Adenoma Adermatoglyphia Adie Pupil Adrenal Gland Pheochromocytoma Adult Hepatocellular Carcinoma Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis, Hereditary, Transthyretin-Related Anaplastic Ependymoma Anaplastic Ganglioglioma Androgen Insensitivity Syndrome, Mild Aneurysm Angiocentric Glioma Angiolipoma Angiomatosis Angiomyolipoma Angiomyoma Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Aortic Disease Apert Syndrome Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Asphyxiating Thoracic Dystrophy Asthma Astroblastoma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Attention Deficit-Hyperactivity Disorder Atypical Autism Autism Autism Spectrum Disorder Autosomal Dominant Polycystic Kidney Disease Bednar Tumor Behr Syndrome Benign Ependymoma Bier Spots Bipolar Disorder Birt-Hogg-Dube Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Boerhaave Syndrome Bullous Pemphigoid Calcifying Epithelial Odontogenic Tumor Capgras Syndrome Capillary Malformations, Congenital Carpal Tunnel Syndrome Cerebellar Atrophy, Developmental Delay, and Seizures Cerebral Primitive Neuroectodermal Tumor Cerebritis Cervicitis Chordoid Meningioma Chordoma Chromophobe Renal Cell Carcinoma Clear Cell Ependymoma Clear Cell Papillary Renal Cell Carcinoma Clear Cell Renal Cell Carcinoma Clivus Chordoma Cohen-Gibson Syndrome Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly Congenital Lymphedema Cortical Blindness Cortical Dysplasia, Complex, with Other Brain Malformations 7 Costello Syndrome Cowden Disease Crouzon Syndrome with Acanthosis Nigricans Cutaneous Leiomyosarcoma Cutis Verticis Gyrata Cystic Kidney Disease Dementia Dermatosis Papulosa Nigra Desmoplastic Infantile Ganglioglioma Desmoplastic Small Round Cell Tumor Diabetes Mellitus Diffuse Lipomatosis Dilated Cardiomyopathy Double Discordia Dyschromatosis Universalis Hereditaria Dysembryoplastic Neuroepithelial Tumor Ehlers-Danlos Syndrome Embryonal Rhabdomyosarcoma Encephalitis Encephalocele Encephalopathy Endometrial Adenocarcinoma Endotheliitis End Stage Renal Failure Ependymoma Epidermoid Cysts Epilepsy Epithelioid Leiomyosarcoma Epulis Estrogen-Receptor Positive Breast Cancer Extracranial Carotid Artery Aneurysm Extraventricular Neurocytoma Fanconi Anemia, Complementation Group E Fanconi Syndrome Febrile Seizures Fetishism Fibrillary Astrocytoma Fibromatosis Fibrous Dysplasia Fibrous Histiocytoma Fibrous Meningioma Focal Cortical Dysplasia, Type Ii Focal Epilepsy Fragile X Syndrome Frontotemporal Dementia Ganglioglioma Ganglioneuroma Gastric Adenocarcinoma Gemistocytic Astrocytoma Giant Cell Tumor Gigantism Gingival Overgrowth Gingivitis Gliofibroma Glioma Glioma Susceptibility 1 Granular Cell Tumor Granulosa Cell Tumor of the Ovary Head Injury Heart Cancer Hemangioblastoma Hemimegalencephaly Hepatic Adenomas, Familial Hepatic Angiomyolipoma Hepatitis Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hereditary Hemorrhagic Telangiectasia Hidradenoma Histiocytoma Horseshoe Kidney Hydrocephalus Hydromyelia Hydrops Fetalis, Nonimmune Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hyperparathyroidism Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypomelanosis of Ito Hypoxia Infertility Insulinoma Intracranial Aneurysm Intracranial Cysts Islet Cell Tumor Juvenile Type Testicular Granulosa Cell Tumor Keratoconus Kidney Angiomyolipoma Kidney Benign Neoplasm Kidney Cancer Klippel-Trenaunay-Weber Syndrome Learning Disability Leiomyoma Leiomyomatosis Leiomyosarcoma Lennox-Gastaut Syndrome Lentigo Maligna Melanoma Leukemia Leydig Cell Tumor Lipomatosis Lissencephaly with Cerebellar Hypoplasia Lung Benign Neoplasm Lung Combined Type Small Cell Carcinoma Lung Disease Lung Leiomyoma Lupus Erythematosus Lymphangiectasia, Intestinal Lymphangioleiomyomatosis Lymphangioma Lymphatic Malformations Lymphedema Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Malignant Glandular Tumor of Peripheral Nerve Sheath Malignant Triton Tumor Mediastinitis Medulloblastoma Medulloepithelioma Megalencephaly Melanoma Melanotic Neuroectodermal Tumor Meningioma, Familial Meningitis Microcephaly, Epilepsy, and Diabetes Syndrome Mononeuropathy of the Median Nerve, Mild Mucolipidosis Iii Alpha/beta Mucolipidosis Iii Gamma Mutism Myoepithelioma Myxopapillary Ependymoma Nail-Patella Syndrome Nephrocalcinosis Nervous System Cancer Neurilemmoma Neuroblastoma Neuroendocrine Tumor Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuronitis Nevus Anemicus Obsessive-Compulsive Disorder Obstructive Hydrocephalus Odontogenic Myxoma Oncocytoma Optic Nerve Glioma Ossifying Fibroma Osteomalacia Pachygyria Pancreatic Cancer Pancreatic Gastrinoma Pancreatic Islet Cell Tumors Pancreatic Neuroendocrine Tumor Pancreatic Somatostatinoma Pancreatitis Pancytopenia Papillary Carcinoma Papillary Ependymoma Papilledema Papilloma of Choroid Plexus Paraganglioma Parathyroid Adenoma Pericardial Mesothelioma Pericoronitis Perineurioma Perivascular Epithelioid Cell Tumor Periventricular Nodular Heterotopia Persistent Hyperplastic Primary Vitreous Pervasive Developmental Disorder Peutz-Jeghers Syndrome Pheochromocytoma Pilocytic Astrocytoma Pineocytoma Placental Abruption Pleomorphic Adenoma Pleomorphic Xanthoastrocytoma Pneumonia Pneumothorax Polycystic Kidney Disease Polycystic Kidney Disease 1 Polycystic Kidney Disease, Infantile Severe, with Tuberous Sclerosis Polymicrogyria Portal Hypertension Portal Vein Thrombosis Precocious Puberty Primary Hepatic Neuroendocrine Carcinoma Primary Hyperparathyroidism Primary Intestinal Lymphangiectasia Primitive Neuroectodermal Tumor of the Cervix Uteri Prostate Cancer Prostatitis Protein C Deficiency Pseudoainhum Pulmonary Edema Pyelonephritis Rasmussen Encephalitis Refractive Error Renal Clear Cell Carcinoma Renal Dysplasia Renal Oncocytoma Renal Tubular Acidosis Retinitis Rett Syndrome Rhabdoid Meningioma Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Sarcoma Schizencephaly Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Situs Inversus Sleep Disorder Somatostatinoma Spina Bifida Occulta Status Epilepticus Strabismus Sturge-Weber Syndrome Subependymal Giant Cell Astrocytoma Subependymal Glioma Subependymoma Subvalvular Aortic Stenosis Syringocystadenoma Papilliferum Syringoma Systemic Lupus Erythematosus Telangiectasis Testicular Cancer Thrombosis Thyroiditis Transitional Cell Carcinoma Transposition of the Great Arteries Triple-Receptor Negative Breast Cancer Tuberous Sclerosis 1 Tuberous Sclerosis 2 Turner Syndrome Uremia Ventricular Septal Defect Vitelliform Macular Dystrophy Vitreoretinopathy, Neovascular Inflammatory Von Hippel-Lindau Syndrome Weber Syndrome West Syndrome Wilms Tumor 6 Wolff-Parkinson-White Syndrome