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Ontology Browser

Term:
MYOPATHY, CONGENITAL, WITH TREMOR (DOID:9004398)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Tremor +     
Compton-North congenital myopathy  
congenital fiber-type disproportion +   
Congenital Myopathy with Excess of Muscle Spindles  
Congenital Myopathy with Fast-Twitch (Type ii) Fiber Atrophy  
cylindrical spirals myopathy 
early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome  
essential tremor +   
fragile X-associated tremor/ataxia syndrome  
Geniospasm 
hyaline body myopathy +   
MYOPATHY, CONGENITAL, WITH TREMOR  
An autosomal dominant muscle disorder characterized by onset of hypotonia and tremor in infancy. Patients have mildly delayed walking, unsteady gait, proximal muscle weakness, and a high-frequency tremor of the limbs.
myotonia congenita +   
Primary Orthostatic Tremor 
Progressive Congenital Myopathy with Scoliosis  
Tremor of Intention, Ataxia, and Lipofuscinosis 
tubular aggregate myopathy  

Synonyms
Exact Synonyms: MYOGENIC TREMOR ;   MYOTREM ;   congenital myopathy with tremor
Primary IDs: OMIM:618524
Definition Sources: OMIM:618524

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