Disease #02790 (CDG1L (glycosylation, congenital disorder of, type Il (CDG-1L)), OMIM:608776)
Official abbreviation |
CDG1L |
Name |
glycosylation, congenital disorder of, type Il (CDG-1L) |
OMIM ID |
608776 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
ALG9 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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