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glycogen storage disease Ia
Summary
- Definition
- A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PC gene, which encodes glucose-6-phosphatase (G6Pase), on chromosome 17q21.
- Super Class
- autosomal recessive disease glycogen storage disease I
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 5836 | PYGL | glycogen phosphorylase L | |
| 5837 | PYGM | glycogen phosphorylase, muscle associated | |
| 6476 | SI | sucrase-isomaltase | |
| 6514 | SLC2A2 | solute carrier family 2 member 2 | |
| 6517 | SLC2A4 | solute carrier family 2 member 4 | |
| 6519 | SLC3A1 | solute carrier family 3 member 1 | |
| 7086 | TKT | transketolase | |
| 7355 | SLC35A2 | solute carrier family 35 member A2 | |
| 7360 | UGP2 | UDP-glucose pyrophosphorylase 2 | |
| 7368 | UGT8 | UDP glycosyltransferase 8 |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000991 | Xanthomatosis |
