Autosomal dominant hereditary disorder
Congenital myopathy with fiber type disproportion
Developmental hereditary disorder
Hereditary disorder of musculoskeletal system
||||
Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation (disorder)
Congenital fiber-type disproportion myopathy due to MYH7 mutation
Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation
Congenital myopathy with fiber-type disproportion associated with the MYH7 (myosin heavy chain 7) gene on the cytogenetic location 14q11.2 inherited in an autosomal dominant manner.
Id1209168005
StatusPrimitive
Associated morphologyMorphologically abnormal structure
Finding siteSkeletal muscle structure
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
TargetG71.2
RuleTRUE
AdviceALWAYS G71.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified