Dolichol kinase deficiency (Q90006): 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/431935004 / rank | |||
Normal rank | |||
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. |
