Autosomal recessive hereditary disorder
Congenital myopathy
Disorder of skeletal muscle
Glycogen storage disease
Hereditary disorder of musculoskeletal system
Hereditary myopathy
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Glycogen storage disease due to lactate dehydrogenase deficiency (disorder)
Glycogen storage disease due to lactate dehydrogenase deficiency
Glycogen storage disease type XI
glycogeenstapelingsziekte door deficiëntie van lactaatdehydrogenase
glycogeenstapelingsziekte door LDH-deficiëntie
glycogeenstapelingsziekte type XI
glycogenose type 11
Id1186809004
StatusPrimitive
Due toLactate dehydrogenase deficiency
Finding siteSkeletal muscle structure
OccurrenceCongenital
ICD-10 complex map reference set
TargetE74.4
RuleTRUE
AdviceALWAYS E74.4
CorrelationSNOMED CT source code to target map code correlation not specified