Glycogen Storage Disease Type Vi
Disease ID: disease_node_3530
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:E74.09, MESH:D006013, MIM:232700, NCI:C126875, ORDO:369, SNOMEDCT_US_2023_03_01:29291001, UMLS_CUI:C0017925 |
|---|---|
| Subclassof | DOID_2747, DOID_0050737 |
| Data Source | DOID, MESH |
| Synonyms | Glycogen storage disease 6, Hers' disease, glycogen storage disease type VI, hepatic glycogen phosphorylase deficiency, hepatophosphorylase deficiency glycogenosis |
| Mesh Id | D006013 |
| Mesh Label | Glycogen Storage Disease Type VI |
| Mesh Subclassof | D006008 |
| Doid Label | glycogen storage disease VI |
| Doid Description | A glycogen storage disease characterized by enlargement of the liver, moderately low blood sugar, elevated levels of acetone and other ketone bodies in the blood and moderate growth retardation. Xref MGI. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_3530 |
| Doid Id | DOID_2754 |
| Label | Glycogen Storage Disease Type Vi |
- Outgoing r'ship
SUBCLASS_OFto/from Glycogen Storage Disease(ID:disease_node_3514) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)