Informaţii despre

Nume Familial Partial Lipodystrophy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli metabolice; Boli rare
Clasificare anatomică Malacards Boli cardiovasculare; Boli de piele; Boli endocrine
Boli din aceeaşi familie Familial Partial Lipodystrophy Due to Akt2 Mutations; Lipodystrophy, Familial Partial, Type 1; Lipodystrophy, Familial Partial, Type 2; Lipodystrophy, Familial Partial, Type 3; Lipodystrophy, Familial Partial, Type 4; Lipodystrophy, Familial Partial, Type 5; Lipodystrophy, Familial Partial, Type 6; Lipodystrophy, Partial, Acquired

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Abdominal Obesity-Metabolic Syndrome 1 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 Acanthosis Nigricans Acquired Metabolic Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alstrom Syndrome Aniridia 1 Anorexia Nervosa 1 Anovulation Arthrochalasia Ehlers-Danlos Syndrome Autosomal Dominant Limb-Girdle Muscular Dystrophy Berardinelli-Seip Congenital Lipodystrophy Blood Group--Ahonen Blood Group, Dombrock 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 Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1h Congenital Generalized Lipodystrophy Diabetes Mellitus Dilated Cardiomyopathy Eclampsia Emerinopathy Emery-Dreifuss Muscular Dystrophy Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant Fanconi Anemia, Complementation Group E Focal Segmental Glomerulosclerosis Follicular Lymphoma Glomerulonephritis Glucose Metabolism Disease Hepatitis Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Juvenile Hereditary Hemochromatosis Lipid Metabolism Disorder Lipodystrophy Lipodystrophy, Familial Partial, Type 1 Lipodystrophy, Familial Partial, Type 2 Lipodystrophy, Familial Partial, Type 3 Lutheran Suppressor, X-Linked Lymphoma Morbid Obesity Muscular Dystrophy Muscular Dystrophy, Limb-Girdle, Type 1b Myopathy, Proximal, and Ophthalmoplegia Overnutrition Pancreatitis Pelger-Huet Anomaly Pigmentation Disease Placental Choriocarcinoma Polycystic Ovary Syndrome Prediabetes Syndrome Pre-Eclampsia Restrictive Dermopathy, Lethal Sleep Apnea Spastic Paraplegia 17, Autosomal Dominant Thyroiditis Vascular Disease