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congenital disorder of glycosylation type 1G
Also see congenital disorder of glycosylation
Genetics:
- associated with mutation in gene for ALG12
Related
dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichyl-alpha-1,6-mannosyltransferase (mannosyltransferase ALG12 homolog, hALG12, membrane protein SB87, ALG12)
General
congenital disorder of glycosylation
Database Correlations
OMIM 607143
References
OMIM :accession 607143