Disease #01821 (GSD1C (glycogen storage disease, type IC (GSD1C)), OMIM:232240)
| Official abbreviation |
GSD1C |
| Name |
glycogen storage disease, type IC (GSD1C) |
| OMIM ID |
232240 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC37A4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-02-03 14:20:40 +01:00 (CET) |
Individuals
|