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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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5-oxoprolinuria
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CN030166 |
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GSSD
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CN030166 |
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Pyroglutamicaciduria
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CN030166 |
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pyroglutamicaciduria
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CN030166 |
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oxoprolinase deficiency
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CN030166 |
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pyroglutamic aciduria
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CN030166 |
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inborn glutathione synthase activity disorder
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CN030166 |
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Inherited glutathione synthetase deficiency
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CN030166 |
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inherited glutathione synthetase deficiency
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CN030166 |
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Glutathione synthetase deficiency
|
CN030166 |
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glutathione synthetase deficiency
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CN030166 |
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rare inborn error of glutathione synthase activity
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CN030166 |
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inborn error of glutathione synthase activity
|
CN030166 |
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