Disease #03232 (GSD9C (storage disease, glycogen, type IXc (GSD-9C)), OMIM:613027)
Official abbreviation |
GSD9C |
Name |
storage disease, glycogen, type IXc (GSD-9C) |
OMIM ID |
613027 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
23 |
Phenotype entries for this disease |
20 |
Associated with 1 gene |
PHKG2 |
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
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