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Ontology Browser

Term:
myopathy, lactic acidosis, and sideroblastic anemia (DOID:0080099)
Annotations: Rat: (4) Mouse: (4) Human: (4) Chinchilla: (3) Bonobo: (3) Dog: (4) Squirrel: (3) Pig: (4)
Parent Terms Term With Siblings Child Terms
MELAS syndrome +     
myopathy +     
Alcohol Myopathy  
centronuclear myopathy +   
congenital myopathy +   
congenital structural myopathy +   
Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy and Myopathy  
MERRF/MELAS Overlap Syndrome  
mitochondrial myopathy +   
Multiple Epiphyseal Dysplasia with Myopathy 
muscular atrophy +   
muscular dystrophy +   
myofascial pain syndrome +   
myofibrillar myopathy +   
myoglobinuria +   
Myopathy due to Malate-Aspartate Shuttle Defect 
MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  
myopathy of extraocular muscle +   
myopathy with extrapyramidal signs  
Myopathy with Giant Abnormal Mitochondria 
Myopathy, Cataract, Hypogonadism Syndrome 
myopathy, lactic acidosis, and sideroblastic anemia +   
myositis +   
Myostitis 
polymyalgia rheumatica  
reducing body myopathy +   
Secretory Diarrhea, Myopathy, and Deafness 
spheroid body myopathy  
X-linked myopathy with excessive autophagy  

Synonyms
Exact Synonyms: HEREDITARY SIDEROBLASTIC ANEMIA WITH MYOPATHY AND LACTIC ACIDOSIS ;   MLASA ;   Mitochondrial myopathy and sideroblastic anemia
Primary IDs: MESH:C536101
Alternate IDs: RDO:0001536
Xrefs: OMIM:PS600462

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