Informaţii despre

Nume Ataxia-Telangiectasia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Cerebellar ataxia with defective DNA repair
Clasificare anatomică Malacards Boli ale ochiului; Boli ale sistemului imunitar; Boli ale sistemului reproducator; Boli ale urechii; Boli de piele; Boli de sânge; Boli endocrine; Boli neuronale
Boli din aceeaşi familie Ataxia-Telangiectasia-Like Disorder 1; Ataxia-Telangiectasia-Like Disorder 2

Vezi şi

Boli A-Z Acardia Aceruloplasminemia Acute Leukemia Acute Liver Failure Acute Lymphocytic Leukemia Adenocarcinoma Adie Pupil Agammaglobulinemia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alpha-Thalassemia/mental Retardation Syndrome, X-Linked Alport Syndrome, X-Linked Al-Raqad Syndrome Andersen Cardiodysrhythmic Periodic Paralysis Aniridia 1 Anorexia Nervosa 1 Apraxia Artemis Deficiency Arterial Tortuosity Syndrome Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia Ataxia-Microcephaly-Cataract Syndrome Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia-Like Disorder 1 Autonomic Dysfunction Autosomal Recessive Cerebellar Ataxia B-Cell Lymphomas Bilateral Breast Cancer Biliary Atresia Bladder Cancer Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bloom Syndrome Brain Edema Brca1 Hereditary Breast and Ovarian Cancer Syndrome Breast Cancer Breast-Ovarian Cancer, Familial 1 Bronchopneumonia Burkitt Lymphoma Cataract Cerebellar Degeneration Cerebral Palsy Cerebritis Cervical Cancer Cervical Dystonia Cervicitis Childhood Leukemia Cholestasis-Lymphedema Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chromosomal Triplication Chronic Eosinophilic Pneumonia Cleft Larynx, Posterior Cockayne Syndrome Colorectal Cancer Cowden Disease Craniopharyngioma Cystic Fibrosis Cystitis Diabetes Mellitus Diffuse Large B-Cell Lymphoma Down Syndrome Dyschromatosis Symmetrica Hereditaria Dystonia Endodermal Sinus Tumor Endotheliitis Eosinophilic Pneumonia Esophageal Cancer Familial Retinoblastoma Gastric Cancer Glioblastoma Glioblastoma Multiforme Glioma Gonadoblastoma Granulocytopenia Growth Hormone Deficiency Hair Disease Hashimoto Thyroiditis Hemolytic Anemia Hemorrhagic Cystitis Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatoblastoma Hepatocellular Carcinoma Hereditary Ataxia Hereditary Breast Ovarian Cancer Syndrome Hereditary Wilms' Tumor Herpes Simplex Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Human Immunodeficiency Virus Type 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypogonadism Hypoxia Ichthyosis Prematurity Syndrome Immunoglobulin Alpha Deficiency Incontinentia Pigmenti Insulin-Like Growth Factor I Interstitial Lung Disease Laryngitis Leiomyosarcoma Leukemia Leukodystrophy Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Lig4 Syndrome Light Fixation Seizure Syndrome Liver Disease Lung Cancer Lung Cancer Susceptibility 1 Lung Disease Lymphoblastic Leukemia Lymphoma Lymphoma, Hodgkin, Classic Lymphoma, Mucosa-Associated Lymphoid Type Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Malignant Pleural Mesothelioma Mantle Cell Lymphoma Megalencephaly Melanoma Microcephaly Mucositis Multiple Mitochondrial Dysfunctions Syndrome 5 Muscular Atrophy Mutagen Sensitivity Myeloid Leukemia Myocardial Infarction Myoclonus Myoepithelioma Myxosarcoma Necrobiosis Lipoidica Neuroblastoma Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Nicolaides-Baraitser Syndrome Nijmegen Breakage Syndrome Nijmegen Breakage Syndrome-Like Disorder Nodular Regenerative Hyperplasia Nonalcoholic Steatohepatitis Ocular Motor Apraxia Oral Cancer Oromandibular Dystonia Ovarian Cancer Ovarian Gonadoblastoma Ovary Papillary Carcinoma Pancreatitis Papillary Carcinoma Paralytic Poliomyelitis Pharyngitis Pharynx Cancer Pneumonia Poliomyelitis Polykaryocytosis Inducer Premature Ovarian Failure 1 Primary Agammaglobulinemia Prolymphocytic Leukemia Prostatitis Pulmonary Valve Stenosis Purpura Retinitis Retinoblastoma Rhabdomyosarcoma Riddle Syndrome Right Atrial Isomerism Roberts Syndrome Rosacea Seckel Syndrome Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Smith-Mccort Dysplasia 1 Spinal Muscular Atrophy Sporadic Breast Cancer Squamous Cell Carcinoma Suppressor of Tumorigenicity 3 Synchronous Bilateral Breast Carcinoma T Cell Deficiency T-Cell Leukemia T-Cell Lymphoma 1a T-Cell Prolymphocytic Leukemia Telangiectasis Testicular Yolk Sac Tumor Tetraamelia Syndrome, Autosomal Recessive Thrombasthenia Thyroid Cancer, Nonmedullary, 1 Thyroiditis Tumor Suppressor Gene on Chromosome 11 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Werner Syndrome Wilms Tumor 6 X-Ray Sensitivity