Disease #07130 (CDG1DD (glycosylation, congenital disorder of, type 1DD), OMIM:301133)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	CDG1DD
Name	glycosylation, congenital disorder of, type 1DD
OMIM ID	301133
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DHRSX
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-23 09:41:45 +01:00 (CET)
Date last edited	N/A

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