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Name: Solute carrier family 35 member A1 congenital disorder of glycosylation (disorder) See more descriptions.

- Solute carrier family 35 member A1 congenital disorder of glycosylation (disorder)
- Solute carrier family 35 member A1 congenital disorder of glycosylation
- SLC35A1 congenital disorder of glycosylation
- CMP-sialic acid transporter deficiency
- Carbohydrate deficient glycoprotein syndrome type IIf
- Congenital disorder of glycosylation type 2f
- Congenital disorder of glycosylation type IIf
- SLC35A1 (solute carrier family 35 member A1) congenital disorder of glycosylation
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Concept ID: 723624008
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ICD-10 Codes: E778
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