Disease #05462 (CDG1AA (glycosylation, congenital disorder of, type Iaa (CDG1AA)), OMIM:617082)
| Official abbreviation |
CDG1AA |
| Name |
glycosylation, congenital disorder of, type Iaa (CDG1AA) |
| OMIM ID |
617082 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NUS1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2018-07-18 22:50:59 +02:00 (CEST) |
| Date last edited |
2021-10-14 19:33:00 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|