Disease #02762 (CDG1K (glycosylation, congenital disorder of, type Ik (CDG-1K)), OMIM:608540)
Official abbreviation |
CDG1K |
Name |
glycosylation, congenital disorder of, type Ik (CDG-1K) |
OMIM ID |
608540 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
40 |
Phenotype entries for this disease |
39 |
Associated with 1 gene |
ALG1 |
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
|