About: Myotonic Disorder

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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Myotonic Disorder
rdfs:subClassOf	Muscular Diseases Rare Non-Neoplastic Disorder
Has_NICHD_Parent	Connective and Soft Tissue Disorder
Concept_In_Subset	NICHD Terminology Neonatal Research Network Terminology
Semantic_Type	Disease or Syndrome
Preferred_Name	Myotonic Disorder
UMLS_CUI	C0553604
Contributing_Source	NICHD
FULL_SYN	Myotonic DisorderPTNCI Myotonic DisorderPTNICHD
DEFINITION	An inherited or acquired, localized or generalized disorder affecting the muscles. It may be associated with abnormalities in the chloride or sodium channels of the muscles. It is characterized by delayed muscle relaxation following stimulation or contraction. Representative examples include myotonia congenita and myotonic dystrophy.NCI
code	C84913
is rdfs:subClassOf of	Myotonia Congenita Myotonic Dystrophy
is Has_NICHD_Parent of	Myotonic Dystrophy

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