DPM3 congenital disorder of glycosylation (Q94040): Difference between revisions
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Revision as of 09:09, 16 August 2026
Congenital disorder of glycosylation type 1o (CDG-Io) is an extremely rare form of CDG syndrome characterised clinically in the single reported case by muscle weakness, waddling gait, and dilated cardiomyopathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1389256016 |
||
| English | DPM3 congenital disorder of glycosylation |
Congenital disorder of glycosylation type 1o (CDG-Io) is an extremely rare form of CDG syndrome characterised clinically in the single reported case by muscle weakness, waddling gait, and dilated cardiomyopathy. |
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CID11:ID_1389256016
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dki-india-ID_1389256016
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Concluído
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