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Glycogen storage disease due to glycogenin deficiency
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
Synonym(s):
- GSD due to glycogenin deficiency
- GSD type 15
- GSD type XV
- Glycogen storage disease type 15
- Glycogen storage disease type XV
- Glycogenosis due to glycogenin deficiency
- Glycogenosis type 15
- Glycogenosis type XV
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
GYG1 P46976603942
No signs/symptoms info available.