MPDU1-congenital disorder of glycosylation

MONDO:0012211

The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type If is characterized by psychomotor delay, seizures, failure to thrive, and cutaneous and ocular anomalies.

Also known as: CDG syndrome type If, CDG-If, CDG1F, CDGIf, MPDU1-CDG, carbohydrate deficient glycoprotein syndrome type If, congenital disorder of glycosylation type 1f, congenital disorder of glycosylation type If

0 clinical trials for this condition and its sub-types, 0 tagged with MPDU1-congenital disorder of glycosylation itself.

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↑ Disorder of multiple glycosylation (9) ↑ Congenital disorder of glycosylation type I (7)

Including sub-types (0) Tagged with MPDU1-congenital disorder of glycosylation (0)

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