Disease #00544 (GLUT1DS1 (GLUT1 deficiency syndrome, type 1, infantile onset, severe (GLUT1DS-1)), OMIM:606777)
| Official abbreviation |
GLUT1DS1 |
| Name |
GLUT1 deficiency syndrome, type 1, infantile onset, severe (GLUT1DS-1) |
| OMIM ID |
606777 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
9 |
| Associated with 1 gene |
SLC2A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|