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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|