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SLC39A8-CDG
MONDO:0014746Also known as: CDG syndrome type IIn, CDG-IIn, CDG2N, SLC39A8 deficiency, carbohydrate deficient glycoprotein syndrome type IIn, congenital disorder of glycosylation type 2n, congenital disorder of glycosylation type IIn, congenital disorder of glycosylation, type IIn
1 clinical trial for this condition and its sub-types, 0 tagged with SLC39A8-CDG itself.
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↑ Hereditary neurological disease
(5791)
↑ Developmental anomaly of metabolic origin
(384)
↑ Congenital nervous system disorder
(287)
↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(59)
↑ Central nervous system malformation
(51)
↑ Disorder of protein N-glycosylation
(7)
↑ Congenital disorder of glycosylation type II
(3)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.