Diabetes mellitus associated with genetic syndrome
Genetic disease
Mitochondrial myopathy
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Myopathy and diabetes mellitus (disorder)
Myopathy and diabetes mellitus
A rare genetic mitochondrial DNA-related mitochondrial myopathy disorder with characteristics of slowly progressive muscular weakness (proximal greater than distal), predominantly involving the facial muscles and scapular girdle, associated with insulin-dependent diabetes mellitus. Neurological involvement and congenital myopathy may be variably observed. The phenotype is caused by mutation in the mitochondrially-encoded tRNA-glu gene (MTTE).
myopathie en diabetes mellitus
Id783722008
StatusPrimitive
Finding siteSkeletal muscle structure
Associated withGenetic disease
Finding siteStructure of endocrine system
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG71.3
RuleTRUE
AdviceALWAYS G71.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified