ALG6 congenital disorder of glycosylation
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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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CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I, WITH DEFICIENT GLYCOSYLATION OF DOLICHOL-LINKED OLIGOSACCHARIDE
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C2930997 |
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CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I, WITH DEFICIENT GLYCOSYLATION OF DOLICHOL-LINKED OLIGOSACCHARIDE, FORMERLY
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C2930997 |
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CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE V
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C2930997 |
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CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE V, FORMERLY
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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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congenital disorder of glycosylation type 1C
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C2930997 |
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Congenital disorder of glycosylation type 1c
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C2930997 |
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Congenital disorder of glycosylation type Ic
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C2930997 |
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