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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 Ic
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C2930997 |
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Congenital Disorder Of Glycosylation, Type Ic
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C2930997 |
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glucosyltransferase 1 deficiency
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C2930997 |
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Congenital disorder of glycosylation, type Ic
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C2930997 |
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ALG6 congenital disorder of glycosylation
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C2930997 |
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Carbohydrate deficient glycoprotein syndrome type 1c
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C2930997 |
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Carbohydrate deficient glycoprotein syndrome type Ic
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C2930997 |
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carbohydrate deficient glycoprotein syndrome type Ic
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C2930997 |
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Carbohydrate deficient glycoprotein syndrome type V
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C2930997 |
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Congenital Disorder of Glycosylation Type Ic
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C2930997 |
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congenital disorder of glycosylation, type Ic
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C2930997 |
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CDG syndrome type Ic
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C2930997 |
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ALG6-congenital disorder of glycosylation 1C
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C2930997 |
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congenital disorder of glycosylation caused by mutation in ALG6
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C2930997 |
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Congenital disorder of glycosylation type 1C
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C2930997 |
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