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Ontology Browser

Myotonia Congenita, Autosomal Dominant (DOID:9001336)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
myotonia congenita +     
Brody myopathy  
Myotonia Congenita, Autosomal Dominant  
A nondystrophic skeletal muscle disorder characterized by muscle stiffness and an inability of the muscle to relax after voluntary contraction. (OMIM)
Myotonia Congenita, Autosomal Recessive  
Myotonia with Skeletal Abnormalities and Mental Retardation 
Native American myopathy  
Potassium Aggravated Myotonia  

Exact Synonyms: THD ;   THOMSEN DISEASE ;   Thomsen Generalized Myotonia ;   Thomsen's Disease ;   Thomsens disease ;   congenital myotonia, autosomal dominant form ;   generalized myotonia of Thomsen
Primary IDs: OMIM:160800
Alternate IDs: RDO:0008077

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