Dolichol kinase deficiency (Q90006): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A síndrome CDG tipo 1M é uma doença congênita de glicosilação caracterizada por hipotonia muscular e ictiose. | |||
| description / en | description / en | ||
CDG syndrome type Im is a Congenital Disorders of Glycosylation characterised by muscular hypotonia and ichthyosis. | |||
Revision as of 16:56, 15 August 2026
CDG syndrome type Im is a Congenital Disorders of Glycosylation characterised by muscular hypotonia and ichthyosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_431935004 |
||
| English | Dolichol kinase deficiency |
CDG syndrome type Im is a Congenital Disorders of Glycosylation characterised by muscular hypotonia and ichthyosis. |
