Informaţii despre

Nume Lipodystrophy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Lipodystrophy, not elsewhere classified
Clasificare anatomică Malacards Boli de piele; Boli endocrine
Boli din aceeaşi familie Localized Lipodystrophy

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Abdominal Obesity-Metabolic Syndrome 1 Acanthosis Nigricans Acquired Generalized Lipodystrophy Acquired Immunodeficiency Syndrome Acquired Metabolic Disease Acromegaly Acute Pancreatitis Adermatoglyphia Adiposis Dolorosa Adrenomyodystrophy Adult Dermatomyositis Aging Aland Island Eye Disease Alopecia 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 Anauxetic Dysplasia 1 Angiolipoma Angiomatosis Aniridia 1 Anorexia Nervosa 1 Apnea, Obstructive Sleep Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Autoimmune Disease Autoimmune Hepatitis Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Autonomic Dysfunction Berardinelli-Seip Congenital Lipodystrophy 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 Injury Branchiootic Syndrome 1 Brittle Diabetes C3 Glomerulopathy Calcinosis Cardiac Arrhythmia Cataract Cerebellar Degeneration Cervicitis Cholesterol Ester Storage Disease Choroiditis Chromosomal Triplication Clark-Baraitser Syndrome Cockayne Syndrome Congenital Generalized Lipodystrophy Connective Tissue Disease Cutis Verticis Gyrata Cytophagic Histiocytic Panniculitis Darier-White Disease Dermatomyositis Diabetes Mellitus Diencephalic Syndrome Dilated Cardiomyopathy Dystonia Eclampsia Emery-Dreifuss Muscular Dystrophy Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive Encephalopathy Encephalopathy, Progressive, with or Without Lipodystrophy Endocrine Pancreas Disease Endosteal Hyperostosis, Autosomal Dominant Endotheliitis Epidermolysis Bullosa Pruriginosa Epilepsy Epithelial Recurrent Erosion Dystrophy Extrinsic Allergic Alveolitis Familial Partial Lipodystrophy Fanconi Anemia, Complementation Group E Fatty Liver Disease Focal Segmental Glomerulosclerosis Follicular Lymphoma Gas Gangrene Gestational Diabetes Gigantism Glomerulonephritis Glucose Intolerance Glucose Metabolism Disease Growth Hormone Deficiency Gynecomastia Hematopoietic Stem Cell Transplantation Hepatic Adenomas, Familial Hepatitis Human Coronavirus Sensitivity Hutchinson-Gilford Progeria Syndrome Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypogonadism Ichthyosis Idiopathic Edema Idiopathic Recurrent Pericarditis Immunoglobulin E Concentration, Serum Infant Gynecomastia Insulin-Like Growth Factor I Leukemia Leukemia, Chronic Myeloid Lichen Amyloidosis Limb-Girdle Muscular Dystrophy Lipedema Lipid Metabolism Disorder Lipodystrophy, Congenital Generalized, Type 1 Lipodystrophy, Congenital Generalized, Type 2 Lipodystrophy, Congenital Generalized, Type 3 Lipodystrophy, Congenital Generalized, Type 4 Lipodystrophy, Familial Partial, Type 1 Lipodystrophy, Familial Partial, Type 2 Lipodystrophy, Familial Partial, Type 3 Lipodystrophy, Partial, Acquired Lipomatosis Lipomatosis, Multiple Liver Disease Localized Lipodystrophy Localized Scleroderma Long Qt Syndrome Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphoblastic Leukemia Lymphoma Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome Mandibuloacral Dysplasia with Type a Lipodystrophy Marfan Lipodystrophy Syndrome Marfan Syndrome Mass Syndrome Membranoproliferative Glomerulonephritis Meningitis Meningococcal Meningitis Microcytic Anemia Morbid Obesity Multiple Sclerosis Multiple Symmetrical Lipomatosis Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Congenital, Lmna-Related Myocardial Infarction Myoclonus Myoclonus Epilepsy Myopathy Myositis Myospherulosis Neurodegeneration with Brain Iron Accumulation 2a Neuropathy Nicolaides-Baraitser Syndrome Nonalcoholic Steatohepatitis Non-Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis Nontuberculous Mycobacterial Lung Disease Obesity, Hyperphagia, and Developmental Delay Obesity-Hypoventilation Syndrome Optic Atrophy 3, Autosomal Dominant Oral Submucous Fibrosis Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Ovarian Cystadenoma Ovarian Disease Overnutrition Pancreatitis Panniculitis Pelger-Huet Anomaly Pilocytic Astrocytoma Poems Syndrome Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy Polycystic Ovary Syndrome Polydactyly, Postaxial, with Progressive Myopia Prediabetes Syndrome Pre-Eclampsia Progressive Myoclonus Epilepsy Pulmonary Eosinophilia Pulmonary Tuberculosis Restrictive Dermopathy, Lethal Retinitis Reynolds Syndrome Salt and Pepper Developmental Regression Syndrome Scleredema Scleredema Adultorum Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Short Syndrome Sleep Apnea Spastic Paraplegia 17, Autosomal Dominant Spiradenoma Synovitis Systemic Lupus Erythematosus Tay-Sachs Disease Thrombocytopenia Thyroiditis Triple X Syndrome Trisomy 22 Undifferentiated Connective Tissue Disease Vaginitis Vascular Disease Werner Syndrome