SRD5A3 congenital disorder of glycosylation (Q94046): Difference between revisions
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Trata-se de distúrbio congênito SRD5A3 da reação em que um carboidrato, isto é, um doador de glicosil, está ligado a um hidroxil ou outro grupo funcional de outra molécula (um receptor/aceptador de glicosil). | |||
| description / en | description / en | ||
This refers to SRD5A3 congenital disorder of the reaction in which a carbohydrate, i.e. a glycosyl donor, is attached to a hydroxyl or other functional group of another molecule (a glycosyl acceptor). | |||
Revision as of 09:09, 16 August 2026
This refers to SRD5A3 congenital disorder of the reaction in which a carbohydrate, i.e. a glycosyl donor, is attached to a hydroxyl or other functional group of another molecule (a glycosyl acceptor).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2080284881 |
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| English | SRD5A3 congenital disorder of glycosylation |
This refers to SRD5A3 congenital disorder of the reaction in which a carbohydrate, i.e. a glycosyl donor, is attached to a hydroxyl or other functional group of another molecule (a glycosyl acceptor). |
