| Glycogen storage disease due to acid maltase deficiency, late-onset (disorder) | | Glycogen storage disease due to acid maltase deficiency, late-onset | | Glycogen storage disease type II late onset
Pompe disease, late onset
Glycogenosis type II, late onset
Alpha-1,4-glucosidase acid deficiency, late onset
| | Glycogen storage disease due to acid maltase deficiency, late onset (AMDL), a form of Glycogen storage disease due to acid maltase deficiency (AMD), a degenerative metabolic myopathy particularly affecting respiratory and skeletal muscles, is characterized by an accumulation of glycogen in lysosomes. |
| | Id | 722343009 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | E74.0 | | Rule | TRUE | | Advice | ALWAYS E74.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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