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
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