| 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.
|
5-oxoprolinuria
|
CN030166 |
|
|
GSSD
|
CN030166 |
|
|
Pyroglutamicaciduria
|
CN030166 |
|
|
pyroglutamicaciduria
|
CN030166 |
|
|
oxoprolinase deficiency
|
CN030166 |
|
|
pyroglutamic aciduria
|
CN030166 |
|
|
Glutathione synthetase deficiency
|
CN030166 |
|
|
glutathione synthetase deficiency
|
CN030166 |
|
|
rare inborn error of glutathione synthase activity
|
CN030166 |
|
|
inborn error of glutathione synthase activity
|
CN030166 |
|
|
inborn glutathione synthase activity disorder
|
CN030166 |
|
|
Inherited glutathione synthetase deficiency
|
CN030166 |
|
|
inherited glutathione synthetase deficiency
|
CN030166 |
|
