Ontology Browser

Term:
eosinophilia-myalgia syndrome (DOID:998)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (0) Bonobo: (0) Dog: (1) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
Eosinophilia +     
muscular disease +     
Anal Sphincter Myopathy, Internal 
Arthrogryposis +   
atrophic muscular disease +   
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Carey-Fineman-Ziter syndrome  
chronic fatigue syndrome  
Chronic Myeloproliferative Disorder with Eosinophilia  
compartment syndrome +   
Congenital Myopathy with Neuropathy and Deafness  
Contracture +   
Craniomandibular Disorders +   
diaphragm disease +   
Dimauro Disease  
disseminated eosinophilic collagen disease 
Early-Onset Myopathy with Fatal Cardiomyopathy  
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2  
eosinophilia-myalgia syndrome  
A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. Diagnostic features generally include EOSINOPHILIA, myalgia severe enough to limit usual activities of daily living, and the absence of coexisting infectious, autoimmune or other conditions that may induce eosinophilia. Biopsy of affected tissue reveals a microangiopathy associated with diffuse inflammation involving connective tissue. (From Spitzer et al., J Rheumatol Suppl 1996 Oct;46:73-9; Blackburn WD, Semin Arthritis Rheum 1997 Jun;26(6):788-93)
Eosinophilic Enteropathy +   
eosinophilic esophagitis  
Eosinophilic Fasciitis 
eosinophilic gastritis 
Eosinophilic Granuloma 
Eosinophilic Pustular Folliculitis  
Eosinophilic Synovitis 
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
Familial Eosinophilia 
familial periodic paralysis +   
fibromyalgia +   
Fingerprint Body Myopathy 
Gamstorp-Wohlfart syndrome  
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
hypereosinophilic syndrome +   
Hypertrophia Musculorum Vera 
Kimura disease 
Kocher-Debre-Semelaigne Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Lethal Congenital Neutropenia with Eosinophilia 
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
Muscular Hypoplasia, Congenital Universal, of Krabbe 
Musculoskeletal Pain +   
Myalgia +   
myofascial pain syndrome +   
Myopathic Carnitine Deficiency 
myopathy +   
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
Myopathy, Hyaline Body, Autosomal Recessive  
Myopathy, Myosin Storage  
MYOPATHY, SCAPULOHUMEROPERONEAL  
myositis +   
myostatin-related muscle hypertrophy  
myotonic disease +   
neutral lipid storage disease +   
Omenn syndrome  
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Pdgfra-Associated Chronic Eosinophilic Leukemia  
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE  
polymyalgia rheumatica  
Proximal Myopathy with Focal Depletion of Mitochondria 
pulmonary eosinophilia +   
Rhabdomyolysis +   
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Treft Sanborn Carey Syndrome 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Uruguay Faciocardiomusculoskeletal Syndrome  
Vacuolar Myopathy  
very long chain acyl-CoA dehydrogenase deficiency  
Wells Syndrome 

Synonyms
Exact Synonyms: Eosinophilia-Myalgia Syndromes ;   L-Tryptophan-Related Eosinophilia-Myalgia Syndrome ;   L-Tryptophan-Related Eosinophilia-Myalgia Syndromes
Primary IDs: MESH:D016603 ;   RDO:0006980
Xrefs: GARD:6345
Definition Sources: MESH:D016603

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.