Details of Disease | DrugMAP

General Information of Disease (ID: DISP0QHJ)

Disease Name	Congenital disorder of glycosylation, type IIw
Synonyms	CDG2W
Disease Hierarchy	DISEMWE1: Congenital disorder of glycosylation type II DISP0QHJ: Congenital disorder of glycosylation, type IIw
Disease Identifiers	MONDO ID MONDO_0030437 UMLS CUI C5561986 OMIM ID 619525 MedGen ID 1794196

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SLC37A4	DTLHZFU	Strong	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
SLC37A4	OTLCYA32	Strong	Autosomal dominant	[1]
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References

1	SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation. Mol Genet Metab Rep. 2020 Aug 21;25:100636. doi: 10.1016/j.ymgmr.2020.100636. eCollection 2020 Dec.