Disease #01819 (GSD1A (storage disease, glycogen, type 1A (GSD-1A)), OMIM:232200)
Official abbreviation |
GSD1A |
Name |
storage disease, glycogen, type 1A (GSD-1A) |
OMIM ID |
232200 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
G6PC |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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