Lipid Storage Diseases

About the Disease
Lipid Storage Disease, also known as lipoidosis, is related to chanarin-dorfman syndrome and sphingolipidosis. An important gene associated with Lipid Storage Disease is PNPLA2 (Patatin Like Phospholipase Domain Containing 2), and among its related pathways/superpathways are Metabolism and Glucose / Energy Metabolism. The drugs Bezafibrate and Clofibric Acid have been mentioned in the context of this disorder. Affiliated tissues include brain, liver and bone marrow, and related phenotypes are liver/biliary system and homeostasis/metabolism

Common Targets
Tubulin | UGCG | KIT | PNPLA2 | ABHD5 | CYP27A1 | Sphingolipid delta(4)-desaturase (nonspecified subtype) | DEGS2 | DEGS1

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Thrombocythemia, Essential | 3C Syndrome | Cannabis Abuse | Apraxia | Japanese Encephalitis | Prurigo Nodularis | Achromatopsia | Hemorrhoids | Acromesomelic Dysplasia | Hereditary Spastic Paraplegia | Sick Sinus Syndrome | Tay-Sachs Disease | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Leishmaniasis, Visceral | Lipodystrophy | Mucolipidosis Type IV | Hypothyroidism | Ichthyosis Hystrix, Curth-Macklin Type | Epidermolytic Palmoplantar Keratoderma | Sarcoma, Alveolar Soft Part | Osteogenesis Imperfecta | Hepatitis B, Chronic | Sengers Syndrome | Chronic Idiopathic Myelofibrosis | Arteriovenous Malformations | Infantile Neuroaxonal Dystrophy | Chronic Neutrophilic Leukemia | Corneal Edema | Antiphospholipid Syndrome | Patent Ductus Arteriosus | Blue Rubber Bleb Nevus Syndrome | Ganglioneuroma | Stuve-Wiedemann Syndrome | Hypermetropia | Photosensitivity | Hyperhomocysteinemia | Chronic Beryllium Disease | Diarrhea | Necrotizing Autoimmune Myopathy | Bethlem Myopathy | Kaposiform 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Vulvovaginitis | Glutaric Aciduria Type 1 | Anxiety Disorders | Colitis, Microscopic | Hypercalciuria | Sporadic Hemiplegic Migraine | Rickets | Parapsoriasis | Hypotrichosis Simplex | Frontometaphyseal Dysplasia | Polycystic Liver | Myofibrillar Myopathy | Panniculitis | Lathosterolosis | Gastroschisis | Medulloblastoma | Avellino Corneal Dystrophy | Dyslipidemia | Myofibromatosis | Neuroma | Glomerulonephritis, Membranoproliferative | Proximal Symphalangism | Chronic Granulomatous Disease | Uremic Pruritus | Clouston Hidrotic Ectodermal Dysplasia | Hyperostosis | Obesity, Morbid | Agammaglobulinemia | Lactose Intolerance | Retinopathy, Diabetic | Antisynthetase Syndrome | Spondyloarthritis | Diabetes Gestational | Hemimegalencephaly | Atrial Septal Defect | Bullous Pemphigoid | Palmoplantar Keratoderma | Sleep Apnea, Obstructive | Angiosarcoma Of The Breast | Xeroderma Pigmentosum Variant Type | Krabbe Disease | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Spinal 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Tumor | Crigler-Najjar Syndrome | Haim-Munk Syndrome | Mucormycosis | Angioimmunoblastic T-cell Lymphoma | Gastritis | Occipital Neuralgia | Arthritis, Gouty | Sarcoma | Dystonia-parkinsonism, X-linked | Bronchiolitis | Brachial Plexus Neuropathy | Primary Aldosteronism | Snyder-Robinson Syndrome | Anal Fissure | Dengue Shock Syndrome | Carpal Tunnel Syndrome | Leukoplakia | Monilethrix | Chronic Leukemia | Premature Ejaculation | Hypertensive Retinopathy | Antithrombin III Deficiency | Heart Block | Poretti-Boltshauser Syndrome | Scleroderma | Campomelic Dysplasia | Pure Autonomic Failure | Aldosterone Deficiency | Jawad Syndrome | Chronic Lymphocytic Leukemia | Multiple Sclerosis, Secondary Progressive | Familial Isolated Hyperparathyroidism | Thin Basement Membrane Disease | Vitamin A Deficiency | Overactive Bladder | Liddle Syndrome | Myoclonus | Avian Influenza | Primary Hyperoxaluria Type 1 | Chondrodysplasia Punctata 1, X-linked Recessive | Hydrolethalus Syndrome | Acne Vulgaris 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