Subjects who meet the 1994 Fukuda et al. criteria for chronic fatigue syndrome1 as well as 2003 Carruthers et al. criteria for myalgic encephalomyelitis.
"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001015"],"study_history":[null],"attribution":["Principal Investigator - Vincent C. Lombardi, PhD - Nevada Center for Biomedical Research, University of Nevada, NV, USA","Funding Source - R01 AI078234 - National Institutes of Health, Bethesda, MD, USA"],"repository":["dbGaP"],"description_synonyms":["Pilot, other disease, Chronic Fatigue Syndromes, Systemic Exertion Intolerance Disease, Fatigue-Fibromyalgia Syndromes, single-organism developmental process, acetylglucosaminyltransferase-like protein, postnatal development, Goal, Mbp1, mEET, growth and development, Normalcies, LARGE1, Fatigue Syndromes, ME/CFS, froggy, Gyltl1a, Life Quality, Myalgic, diseases, NEDD4 WW domain-binding protein 3, Studies, disease or disorder, Project, diseases and disorders, Postviral Fatigue, systemic exertion intolerance disease, myd, Postviral fatigue syndrome, Health Related Quality Of Life, Normalities, average, study, human disease, like-acetylglucosaminyltransferase, Infectious Mononucleosis Like Syndrome, MDDGB6, CFS, study., Mbp-1, Chronic Fatigue and Immune Dysfunction Syndrome, LARGE, Health-Related Quality Of Life, Chronic Fatigue Fibromyalgia Syndrome, LPS-induced TNF-alpha factor homolog, Chronic Fatigue-Fibromyalgia Syndromes, non-neoplastic, LITAF-like protein, Postviral Fatigue Syndromes, Study, Pilot Project, BPFD#36, Syndrome, Fatigue Disorder, Chronic, disorder, Chronic Fatigue-Fibromyalgia Syndrome, myalgic encephalomeyelitis/chronic fatigue syndrome, Homo sapiens disease, myalgic encephalitis, chronic fatigue immune dysfunction syndrome, Myalgic Encephalomyelitis, Individual Health, Chronic Fatigue Disorder, Infectious Mononucleosis-Like Syndrome, process quality of life cycle, myalgic encephalomyelitis, gyltl1b-b, disorders, Chronic Fatigue Disorders, medical condition, Normalcy, Postviral Fatigue Syndrome, development, Fatigue Syndrome, Fatigue-Fibromyalgia Syndrome, Royal Free Disease, MDDGA6, mKIAA0609, Diseases, condition, Individual, HRQOL, KIAA0609, acetylglucosaminyltransferase-like 1A, fg, Encephalomyelitis, gyltl1b, Projects, SEID, Normality, Chronic Fatigue Syndrome, postnatal growth, mdc1d, LARGE_HUMAN, Postviral, disease, MDC1D, Health, like-glycosyltransferase, enr, Pilot Study, chronic fatigue syndrome, growth, Pilot Studies, Estrogen-enhanced transcript protein, glycosyltransferase-like protein LARGE1"],"additional_accession":[]},"is_claimable":false,"name":"Deciphering the Pathophysiology of Chronic Fatigue Syndrome","description":"Myalgic encephalomyelitis, also known as chronic fatigue syndrome or ME/CFS, is a complex and heterogeneous disease that severely impacts the health and quality of life of those afflicted. Several lines of evidence support the possibility that ME/CFS development may involve a heritable component. In this pilot study, 42 cases that meet the diagnostic criteria of ME/CFS and 38 healthy controls were consented into this study. The goal of this study was to identify candidate polymorphisms that can be used for a large multi-center screening study.
","dates":{"last_modification":"2016-09-27","creation":"2015-10-27"},"accession":"phs001015","cross_references":{"MESH":["Fatigue Syndrome, Chronic"],"PMID":["7978722"]}}