DPM3 congenital disorder of glycosylation (Q94040): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/1389256016 / rank | |||
Normal rank | |||
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. |
