| manager |
|
| language |
- |
| license |
- |
| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
|
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
|
622,528 entries
|
There is 0 pattern entry.
|
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE V, FORMERLY
|
C2930997 |
|
|
Glucosyltransferase 1 deficiency
|
C2930997 |
|
|
glucosyltransferase 1 deficiency
|
C2930997 |
|
|
ALG6 congenital disorder of glycosylation
|
C2930997 |
|
|
Carbohydrate deficient glycoprotein syndrome type 1c
|
C2930997 |
|
|
Carbohydrate deficient glycoprotein syndrome type Ic
|
C2930997 |
|
|
carbohydrate deficient glycoprotein syndrome type Ic
|
C2930997 |
|
|
Carbohydrate deficient glycoprotein syndrome type V
|
C2930997 |
|
|
Congenital Disorder of Glycosylation Type Ic
|
C2930997 |
|
|
ALG6-congenital disorder of glycosylation 1C
|
C2930997 |
|
|
congenital disorder of glycosylation caused by mutation in ALG6
|
C2930997 |
|
|
Congenital disorder of glycosylation type 1C
|
C2930997 |
|
|
congenital disorder of glycosylation type 1C
|
C2930997 |
|
|
Congenital disorder of glycosylation type 1c
|
C2930997 |
|
|
Congenital disorder of glycosylation type Ic
|
C2930997 |
|
