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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 18-10-2022
Symbol CMD1LL
Location 22q11.21
Name cardiomyopathy, dilated, 1LL
Corresponding gene TXNRD2
Main clinical features nonsyndromic dilated cardiomyopathy
Genetic determination not applicable
Function/system disorder cardiovascular
Type disease
Remark(s)