Phosphomannose isomerase deficiency (Q94036): Difference between revisions
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A síndrome CDG tipo 1B é um distúrbio congênito de glicosilação caracterizada por manifestações hepático-intestinais (diarreia, vômito e hepatomegalia associada à fibrose hepática). | |||
| description / en | description / en | ||
CDG syndrome type Ib is a Congenital Disorder of Glycosylation characterised by hepatic-intestinal manifestations (diarrhoea, vomiting, and hepatomegaly associated with hepatic fibrosis). | |||
Revision as of 09:09, 16 August 2026
CDG syndrome type Ib is a Congenital Disorder of Glycosylation characterised by hepatic-intestinal manifestations (diarrhoea, vomiting, and hepatomegaly associated with hepatic fibrosis).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_803079134 |
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| English | Phosphomannose isomerase deficiency |
CDG syndrome type Ib is a Congenital Disorder of Glycosylation characterised by hepatic-intestinal manifestations (diarrhoea, vomiting, and hepatomegaly associated with hepatic fibrosis). |
