| C0349653 |
Congenital disorder of glycosylation type 1A |
DO |
congenital disorder of glycosylation Ia
|
0080552 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
EFO |
congenital disorder of glycosylation type I
|
0005545 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
MONDO |
congenital disorder of glycosylation type I
|
0005500 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
MONDO |
PMM2-CDG
|
0008907 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
MSH |
Congenital disorder of glycosylation type 1A
|
C535739 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
NCI |
CDGIa
|
C126868 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
NCI |
Congenital Disorder of Glycosylation Type Ia
|
C126868 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
OMIM |
JAEKEN SYNDROME
|
212065 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
OMIM |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia
|
212065 |
| C0349653 |
Congenital disorder of glycosylation type 1A |
ORDO |
PMM2-CDG
|
79318 |