Dolichol kinase deficiency (Q90006)
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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
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dki-india-ID_431935004
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Concluído
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13 August 2026
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