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Glycogen storage disease due to acid maltase deficiency, infantile onset
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Glycogen storage disease due to acid maltase deficiency, juvenile onset
1 associated gene
No signs/symptoms info
Glycogen storage disease due to acid maltase deficiency, infantile onset
Glycogen storage disease due to acid maltase deficiency, juvenile onset

GAA
(UniProt - OMIM)
 GAA
(UniProt - OMIM)

COMMON
GENES 		GAA


Citations in the biomedical literature:


Glycogen storage disease due to acid maltase deficiency, infantile onset
GAA
Glycogen storage disease due to acid maltase deficiency, juvenile onset



Glycogen storage disease due to acid maltase deficiency, infantile onset
Glycogen storage disease due to acid maltase deficiency, juvenile onset

Synonym(s):
- Alpha-1,4-glucosidase acid deficiency, infantile onset
- GSD due to acid maltase deficiency, infantile onset
- GSD type 2, infantile onset
- Glycogen storage disease type 2, infantile onset
- Glycogenosis due to acid maltase deficiency, infantile onset
- Glycogenosis type 2, infantile onset
- Pompe disease, infantile onset
Synonym(s):
- Alpha-1,4-glucosidase acid deficiency, juvenile onset
- GSD due to acid maltase deficiency, juvenile onset
- GSD type 2, juvenile onset
- Glycogen storage disease type 2, juvenile onset
- Glycogenosis due to acid maltase deficiency, juvenile onset
- Glycogenosis type 2, juvenile onset
- Pompe disease, juvenile onset
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.