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Term:
Early-Onset Myopathy with Fatal Cardiomyopathy (DOID:9006785)
Annotations: Rat: (1) Mouse: (1) Human: (3) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
cardiomyopathy +     
muscular disease +     
alcoholic cardiomyopathy  
Arthrogryposis +   
Ataxia, Deafness, and Cardiomyopathy 
Atrial Dilation and Standstill +   
atrophic muscular disease +   
autosomal recessive limb-girdle muscular dystrophy type 2D  
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Cardiomyopathy Associated with Myopathy and Sudden Death 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods 
Carey-Fineman-Ziter syndrome  
Chagas Cardiomyopathy  
chronic fatigue syndrome  
compartment syndrome +   
Congenital Myopathy with Neuropathy and Deafness  
Contracture +   
Craniomandibular Disorders +   
Danon disease  
Diabetic Cardiomyopathies  
diaphragm disease +   
Dimauro Disease  
Early-Onset Myopathy with Fatal Cardiomyopathy  
Ehlers-Danlos syndrome kyphoscoliotic type 2  
endocardial fibroelastosis +   
endomyocardial fibrosis  
eosinophilia-myalgia syndrome  
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
extrinsic cardiomyopathy +   
Familial Cardiac Lipidosis 
familial periodic paralysis +   
Fatal Fetal Cardiomyopathy due to Myocardial Calcification 
fibromyalgia +   
Fingerprint Body Myopathy 
Gamstorp-Wohlfart syndrome  
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
Hypertaurinuric Cardiomyopathy 
Hypertrophia Musculorum Vera 
infantile histiocytoid cardiomyopathy  
Internal Anal Sphincter Myopathy 
intrinsic cardiomyopathy +   
Kearns-Sayre syndrome  
Keshan disease  
Kocher-Debre-Semelaigne Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
linear skin defects with multiple congenital anomalies 3  
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Mitochondrial Cardiomyopathy  
mitochondrial DNA depletion syndrome 12a  
mitochondrial DNA depletion syndrome 12b  
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
Muscular Dystrophy, Cardiac Type 
Muscular Hypoplasia, Congenital Universal, of Krabbe 
Musculoskeletal Pain +   
Myalgia +   
Myocardial Reperfusion Injury  
myocarditis +   
myofascial pain syndrome +   
myofibrillar myopathy 2  
Myopathic Carnitine Deficiency 
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
myositis +   
myostatin-related muscle hypertrophy  
myotonic disease +   
Myotoxicity 
neutral lipid storage disease +   
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Proximal Myopathy with Focal Depletion of Mitochondria 
Rhabdomyolysis +   
Roifman Syndrome  
Sengers syndrome  
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  

Synonyms
Exact Synonyms: EOMFC ;   SALMY ;   Salih Cmd ;   Salih Congenital Muscular Dystrophy ;   Salih Myopathy
Primary IDs: MESH:C567129
Alternate IDs: OMIM:611705 ;   RDO:0015288 ;   RDO:0015923

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