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Congenital muscular dystrophy with intellectual disability and severe epilepsy

MONDO:0014023

Also known as: CDG syndrome type Iu, CDG-Iu, CDG1U, CMD with intellectual disability and severe epilepsy, DPM2-CDG, carbohydrate deficient glycoprotein syndrome type Iu, congenital disorder of glycosylation type 1u, congenital disorder of glycosylation type Iu

5 clinical trials for this condition and its sub-types, 0 tagged with Congenital muscular dystrophy with intellectual disability and severe epilepsy itself.

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