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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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Congenital Disorder Of Glycosylation, Type ID
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C1832736 |
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CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE IV
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C1832736 |
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CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE IV, FORMERLY
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C1832736 |
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ALG3-CDG - asparagine-linked glycosylation 3 congenital disorder of glycosylation
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C1832736 |
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Mannosyltransferase 6 deficiency
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C1832736 |
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mannosyltransferase 6 deficiency
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C1832736 |
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ALG3 congenital disorder of glycosylation
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C1832736 |
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Carbohydrate deficient glycoprotein syndrome type Id
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C1832736 |
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carbohydrate deficient glycoprotein syndrome type Id
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C1832736 |
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Congenital Disorder of Glycosylation Type Id
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C1832736 |
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ALG3-congenital disorder of glycosylation
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C1832736 |
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Congenital disorder of glycosylation type 1D
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C1832736 |
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Congenital disorder of glycosylation type 1d
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C1832736 |
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congenital disorder of glycosylation type 1d
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C1832736 |
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Congenital disorder of glycosylation type Id
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C1832736 |
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