DK1 deficiency (medical condition): Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type Im is caused by a defect on chromosome 9q34.11 and involves a defect in the TMEM15 gene.
See also:
Congenital disorder of glycosylation type 1M:
»Introduction: Congenital disorder of glycosylation type 1M
»Symptoms of Congenital disorder of glycosylation type 1M
These medical condition or symptom topics may be relevant to medical information for DK1 deficiency:
DK1 deficiency: Another name for Congenital disorder of glycosylation type 1M (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 1M
»Symptoms of Congenital disorder of glycosylation type 1M
Some of the symptoms of DK1 deficiency incude:
See full list of 15 symptoms of DK1 deficiency (Congenital disorder of glycosylation type 1M)
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