Familial Partial Lipodystrophy

About the Disease
Familial Partial Lipodystrophy, also known as lipodystrophy, familial partial, is related to lipodystrophy, familial partial, type 1 and lipodystrophy, familial partial, type 6, and has symptoms including myalgia An important gene associated with Familial Partial Lipodystrophy is LMNA (Lamin A/C), and among its related pathways/superpathways are Metabolism and Signal Transduction. The drugs Chenodeoxycholic acid and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include skin, liver and pancreas, and related phenotypes are no effect and no effect

Common Targets
ANGPTL3 | PPARG | Peroxisome Proliferator-Activated Receptors (PPAR) (nonspecified subtype) | APOC3 | LEPR | PNPLA2 | LMNA | PLIN1 | LIPE | POLD1

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3C Syndrome | Apparent Mineralocorticoid Excess Syndrome | Asthma, Exercise-induced | Allergic Contact Dermatitis | Hernia, Inguinal | Isobutyryl-CoA Dehydrogenase Deficiency | Pleural Tuberculosis | Celiac Disease | Iron Overload | Adrenomyeloneuropathy | Cancer, Brain | Histoplasmosis | Oligospermia | Pilomatrix Carcinoma | Cranial Nerve Disease | Non-proliferative Diabetic Retinopathy | Hypertension, Essential | Crimean-Congo Hemorrhagic Fever | Creatine Deficiency Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Amelanotic Melanoma | Rotor Syndrome | Congenital Nephrotic Syndrome | Acromesomelic Dysplasia | Retinopathy, Diabetic | Glycogen Storage Disease Type 0, Muscle | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Paroxysmal Nocturnal Hemoglobinuria | Ebstein Anomaly | Pyloric Stenosis, Infantile Hypertrophic | Congenital Myopathy | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Syphilis | Riboflavin Transporter Deficiency Neuronopathy | 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Hypercalciuria | Kleine-Levin Syndrome | Cardiomyopathy, Restrictive | Gangliosidosis, GM1 | Keratosis, Seborrheic | Distal Myopathy | Spondylo-ocular Syndrome | Systemic Mastocytosis | Chondrodysplasia Punctata 2, X-linked Dominant | Rosacea | Thrombotic Microangiopathy | Hypokalemia | Dysgerminoma | Malignant Peripheral Nerve Sheath Tumor | Aspartylglycosaminuria | Globozoospermia | Split Hand-foot Malformation | Parkinson Disease 6, Autosomal Recessive Early-onset | Liver Diseases | Glycogen Storage Disease Type 3 | Endophthalmitis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | IgA Nephropathy | Crisponi Syndrome | Blastoma, Pleuropulmonary | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Hemangioblastoma | Ameloblastic Carcinoma | Fibronectin Glomerulopathy | Lactose Intolerance | Pre-eclampsia | Megaloblastic Anemia | Lafora Disease | Glucagonoma | Retinitis | Molybdenum Cofactor Deficiency | Keratosis, Actinic | Cardiospondylocarpofacial Syndrome | Pneumonia, 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