Disease #01690 (CDG2A (glycosylation, congenital disorder of, type IIa (CDG-2A)), OMIM:212066)
| Official abbreviation |
CDG2A |
| Name |
glycosylation, congenital disorder of, type IIa (CDG-2A) |
| OMIM ID |
212066 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
MGAT2 |
| 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.
|