Dolichol kinase deficiency (Q90006)
From determinar.ia.br - Determine suas informações
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. |
Statements
CID11:ID_431935004
0 references
