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
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