Informaţii despre

Nume Glycogen Storage Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Glycogen storage disease
Clasificare anatomică Malacards Boli cardiovasculare; Boli de sânge; Boli endocrine; Boli hepatice; Boli musculare; Boli nefrologice (ale rinichilor); Boli neuronale
Boli din aceeaşi familie Glycogen Storage Disease Ia; Glycogen Storage Disease Ib; Glycogen Storage Disease Ic; Glycogen Storage Disease Ii; Glycogen Storage Disease Iii; Glycogen Storage Disease Iv; Glycogen Storage Disease Ix; Glycogen Storage Disease Ixa; Glycogen Storage Disease Ixb; Glycogen Storage Disease Ixc; Glycogen Storage Disease Type 0; Glycogen Storage Disease V; Glycogen Storage Disease Vi; Glycogen Storage Disease Vii; Glycogen Storage Disease Viii; Glycogen Storage Disease X; Glycogen Storage Disease Xii; Glycogen Storage Disease Xiii; Glycogen Storage Disease Xv; Glycogen Storage Disease, Type Ixd

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Acrocallosal Syndrome Acute Pancreatitis Adenoma Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amyloidosis Amyotonia Congenita Anauxetic Dysplasia 1 Aneurysm Aniridia 1 Anorexia Nervosa 1 Apolipoprotein C-Iii Deficiency Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Biliary Atresia Biotin Deficiency Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Candidiasis Carbohydrate Metabolic Disorder Carnitine Deficiency, Systemic Primary Castleman Disease Cerebrovascular Disease Cleft Lip Colitis Costello Syndrome Crohn's Colitis Crohn's Disease Cystic Angiomatosis of Bone, Diffuse Danon Disease Deoxyguanosine Kinase Deficiency Diabetes Mellitus Endotheliitis Epilepsy Familial Hyperlipidemia Fanconi-Bickel Syndrome Fanconi Syndrome Fasting Hypoglycemia Fructose-1,6-Bisphosphatase Deficiency Galactose Epimerase Deficiency Gardner-Diamond Syndrome Gastric Cancer Gerstmann-Straussler Disease Glycogen Storage Disease 0, Liver Glycogen Storage Disease 0, Muscle Glycogen Storage Disease Due to Liver Phosphorylase Kinase Deficiency Glycogen Storage Disease Ia Glycogen Storage Disease Ib Glycogen Storage Disease Ic Glycogen Storage Disease Ii Glycogen Storage Disease Iii Glycogen Storage Disease Iv Glycogen Storage Disease Ixa Glycogen Storage Disease Ixa1 Glycogen Storage Disease Type 0 Glycogen Storage Disease V Glycogen Storage Disease Vi Glycogen Storage Disease Vii Glycogen Storage Disease X Gout Growth Hormone Deficiency Hepatic Adenomas, Familial Hepatitis Hepatoblastoma Hepatocellular Adenoma Hepatocellular Carcinoma Holocarboxylase Synthetase Deficiency Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hypercholesterolemia, Autosomal Dominant, 3 Hyperglycemia Hyperinsulinism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypotonia Inflammatory Bowel Disease Inflammatory Bowel Disease 1 Kwashiorkor Lactic Acidosis Laryngeal Cleft Leukemia Liver Cirrhosis Liver Disease Macroglossia Medulloblastoma Mitochondrial Myopathy Muscle Disorders Myasthenia Gravis Myeloid Leukemia Myoclonic Epilepsy of Lafora Myoclonus Myoclonus Epilepsy Myopathy Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Neuropathy Neutropenia Neutrophilia, Hereditary Niemann-Pick Disease Pancreatitis Paraplegia Peliosis Hepatis Pfeiffer Syndrome Phenylketonuria Phosphoglycerate Kinase Deficiency Phosphoglycerate Mutase Deficiency Phosphorylase Kinase Deficiency Pick Disease of Brain Pituitary Hypoplasia Progressive Myoclonus Epilepsy Pulmonary Hypertension Renal Fibrosis Rheumatic Fever Rheumatic Fever-Related Antigen Sickle Cell Anemia Syncope Tendinitis Thyroiditis Ulcerative Colitis Undifferentiated Pleomorphic Sarcoma Xanthomatosis