Informaţii despre

Nume Hypoglycemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice
Clasificari ICD10 Hypoglycaemia, unspecified
Clasificare anatomică Malacards Boli endocrine

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Acinar Cell Carcinoma Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acromegaly Actn3 Deficiency Acute Ackee Fruit Intoxication Acute Diarrhea Acute Generalized Exanthematous Pustulosis Acute Insulin Response Acute Mountain Sickness Acute Myocardial Infarction Acute Pancreatitis Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of Adenocarcinoma Adenohypophysitis Adenoma Adrenal Carcinoma Agammaglobulinemia Aging Al Amyloidosis Alcoholic Hepatitis 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 Amenorrhea Amyloidosis Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anoxia Aromatic L-Amino Acid Decarboxylase Deficiency Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Autonomic Dysfunction Autonomic Neuropathy Babesiosis Bartonellosis B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas Beckwith-Wiedemann Syndrome Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System 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 Brain Edema Brain Injury Brain Ischemia Breast Cancer Carbohydrate Metabolic Disorder Carcinoid Syndrome Carcinoid Tumors, Intestinal Cardiac Arrest Cardiac Arrhythmia Cardiomyopathy, Dilated, 1o Carnitine-Acylcarnitine Translocase Deficiency Carnitine Palmitoyltransferase Ii Deficiency, Infantile Cataract Central Hypoventilation Syndrome, Congenital Central Pontine Myelinolysis Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Charge Syndrome Cholangiocarcinoma Cholestasis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chronic Fatigue Syndrome Coats Disease Colon Adenocarcinoma Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Giant Megaureter Congenital Human Immunodeficiency Virus Congenital Syphilis Congestive Heart Failure Cortical Blindness Costello Syndrome Craniopharyngioma Cystadenocarcinoma Cystic Fibrosis Dementia Desmoplastic Small Round Cell Tumor Diabetes Mellitus Diabetes Mellitus, Insulin-Dependent Diabetes Mellitus, Noninsulin-Dependent Diabetes Mellitus, Permanent Neonatal Diabetes Mellitus, Transient Neonatal, 1 Diabetic Autonomic Neuropathy Diarrhea Differentiated Thyroid Carcinoma Differentiating Neuroblastoma Diffuse Large B-Cell Lymphoma Disseminated Intravascular Coagulation Donnai-Barrow Syndrome Drug-Induced Lupus Erythematosus Dumping Syndrome Duodenal Ulcer Duodenitis Dwarfism Encephalopathy Endocrine Pancreas Disease Endotheliitis Epilepsy Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Factitious Disorder Familial Paroxysmal Nonkinesigenic Dyskinesia Fanconi Anemia, Complementation Group E Fanconi-Bickel Syndrome Fanconi Syndrome Fasting Hypoglycemia Febrile Seizures Fetal Macrosomia Fibrosarcoma Fibrosarcoma of Bone Fibrous Histiocytoma Fructose-1,6-Bisphosphatase Deficiency Galactosemia Gastric Adenocarcinoma Gastric Cancer Gastric Leiomyosarcoma Gastrointestinal Stromal Tumor Gastrointestinal System Disease Generalized Anxiety Disorder Gestational Diabetes Gigantism Glucagonoma Glucose Intolerance Glucose Transporter Type 1 Deficiency Syndrome Glycogen Storage Disease Glycogen Storage Disease 0, Liver Glycogen Storage Disease Iii Glycogen Storage Disease Type 0 Gonadal Dysgenesis Graves' Disease Griscelli Syndrome Growth Hormone Deficiency Hemangiopericytoma, Malignant Hemiplegia Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatitis C Virus Hepatoblastoma Hepatocellular Carcinoma Histiocytoma Holocarboxylase Synthetase Deficiency Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 1 Hyperinsulinemic Hypoglycemia, Familial, 2 Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinemic Hypoglycemia, Familial, 5 Hyperinsulinemic Hypoglycemia, Familial, 6 Hyperinsulinemic Hypoglycemia, Familial, 7 Hyperinsulinism Hyperproinsulinemia Hyperprolactinemia Hyperthyroidism Hypertrichosis Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoglycemia, Leucine-Induced Hypoglycemic Coma Hypokalemia Hypoparathyroidism Hypophosphatemia Hypopituitarism Hypothalamic Disease Hypotonia Hypoxia Ichthyosis Insulin Autoimmune Syndrome Insulin-Like Growth Factor I Insulinoma Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity Interstitial Lung Disease Intrahepatic Cholestasis Ischemia Islet Cell Adenomatosis Islet Cell Tumor Isolated Growth Hormone Deficiency Jamaican Vomiting Sickness Johanson-Blizzard Syndrome Lactic Acidosis Large Cell Carcinoma Leiomyosarcoma Leukemia Liposarcoma Lissencephaly, X-Linked, 1 Liver Cirrhosis Locked-in Syndrome Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Long Qt Syndrome Lung Disease Lupus Erythematosus Lymphoblastic Leukemia Lymphoma Lymphosarcoma Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macroglobulinemia Macroglossia Macular Dystrophy, Retinal, 1, North Carolina Type Maple Syrup Urine Disease Maturity-Onset Diabetes of the Young Maturity-Onset Diabetes of the Young, Type 2 Maturity-Onset Diabetes of the Young, Type 3 Mediastinitis Megalencephaly Mehmo Syndrome Meninges Hemangiopericytoma Meningitis Mesenchymal Cell Neoplasm Metabolic Acidosis Metastatic Insulinoma Methemoglobinemia Microcephaly Mitochondrial Complex Iii Deficiency Mitochondrial Dna Depletion Syndrome 4a Monocarboxylate Transporter 1 Deficiency Monocytic Leukemia Monogenic Diabetes Morbid Obesity Multiple Endocrine Neoplasia Multiple Personality Disorder Mumps Munchausen by Proxy Muscular Dystrophy Myeloma, Multiple Myeloproliferative Syndrome, Transient Myocardial Infarction Myotonic Dystrophy Myxedema Neonatal Diabetes Mellitus Neonatal Thyrotoxicosis Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neurofibrosarcoma Neuronitis Neuropathy Obesity, Hyperphagia, and Developmental Delay Ocular Motor Apraxia Omphalocele Organic Acidemia Pancreatic Agenesis Pancreatic Islet Cell Tumors Pancreatic Neuroendocrine Tumor Pancreatic Somatostatinoma Pancreatitis Pancytopenia Paroxysmal Choreoathetosis Paroxysmal Nonkinesigenic Dyskinesia 1 Pepck 1 Deficiency Peritonitis Perlman Syndrome Persistent Vegetative State Personality Disorder Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Adenoma Pituitary Apoplexy Pituitary Gland Disease Pituitary Tumors Platelet Glycoprotein Iv Deficiency Pleural Cancer Pneumonia Polycystic Kidney Disease Polycystic Ovary Syndrome Polycythemia Polymicrogyria Potter's Syndrome Premature Ovarian Failure 7 Primary Cerebellar Degeneration Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ib Psoriasis Psoriasis 13 Psoriatic Arthritis Psychotic Disorder Pulmonary Blastoma Pulmonary Edema Purpura Pustular Psoriasis Pyloric Stenosis Quadriplegia Renal Cell Carcinoma, Nonpapillary Retinitis Retinitis Pigmentosa Retroperitoneal Hemangiopericytoma Retroperitoneal Liposarcoma Retroperitoneal Sarcoma Reye Syndrome Rheumatoid Arthritis Sarcoidosis 2 Sarcoma Seizure Disorder Seizures, Benign Familial Neonatal, 1 Serotonin Syndrome Serous Cystadenocarcinoma Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sleep Apnea Solid Pseudopapillary Carcinoma of the Pancreas Somatostatinoma Sotos Syndrome 1 Spindle Cell Sarcoma Spinocerebellar Degeneration Spondylitis Spondyloarthropathy 1 Status Epilepticus Streptococcal Toxic-Shock Syndrome Sveinsson Chorioretinal Atrophy Syphilis Systemic Lupus Erythematosus Teratoma Three M Syndrome 1 Thrombocytopenia Thrombosis Thrombotic Thrombocytopenic Purpura Thyroid Cancer Thyroid Crisis Thyroiditis Toxic Shock Syndrome Turner Syndrome Type 1 Diabetes Mellitus 15 Uremia Urticaria West Syndrome