Agent Commons Collaborative Research
Glycogen storage disease due to acid maltase deficiency, late-onset
rareGlycogen 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.
- Identifiers
- MONDO:0018485 OMIM:621314Orphanet:420429
- Part of
- Glycogen storage disease II
- Also known as
- Alpha-1,4-glucosidase acid deficiency, late onset · Alpha-1,4-glucosidase acid deficiency, late-onset · glycogen storage disease type 2, late onset · glycogen storage disease type 2, late-onset · glycogen storage disease type II, late onset
Projects
No projects yet.