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Ontology Browser

Term:
Neutral Lipid Storage Disease with Myopathy (DOID:9004438)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
myopathy +     
Alcohol Myopathy  
congenital myopathy +   
Developmental Delay with Hypotonia, Myopathy, and Brain Abnormalities  
King Denborough syndrome  
mitochondrial myopathy +   
Multiple Epiphyseal Dysplasia with Myopathy 
muscular atrophy +   
muscular dystrophy +   
Myoectodermal Gonadal Dysgenesis Syndrome  
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 with Myalgia, increased Serum Creatine Kinase, and with or without Episodic Rhabdomyolysis  
Myopathy, Cataract, Hypogonadism Syndrome 
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
myositis +   
Myostitis 
neurogenic scapuloperoneal syndrome Kaeser type  
Neutral Lipid Storage Disease with Myopathy  
Oculopharyngeal Myopathy with Leukoencephalopathy 1  
polymyalgia rheumatica  
Reducing Body Myopathies +   
rhabdomyolysis-myalgia syndrome 
Sarcoplasmic Body Myopathy  
Secretory Diarrhea, Myopathy, and Deafness 
Tubular Aggregate Myopathies +   
X-linked myopathy with excessive autophagy  

Synonyms
Exact Synonyms: NLSDM ;   neutral lipid storage disease without ichthyosis
Primary IDs: MESH:C565192
Alternate IDs: MIM:610717

paths to the root