UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
M M0 M1 M2 M4 M5 M7 M8 M9 MA MB MC MD ME MF MG MH MI MK ML MM MN MO MP MR MS MT MU MV MY
MYA MYB MYC MYD MYE MYH MYI MYL MYO MYP MYR MYT MYX

myotonia congenita

[congenital genetic disease characterized by tonic spasm and rigidity of certain muscles when a voluntary movement is attempted; also known as Thomsen's disease. ( CSP )]
UMLS (CSP) C0027127
 
Disease or Syndrome
Relation/PAR: Genetic Condition
Myotonic disorders
congenital neuromuscular disorder
Heredodegenerative Disorders, Nervous System

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