Disease #05462 (CDG1AA (glycosylation, congenital disorder of, type Iaa (CDG1AA)), OMIM:617082)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CDG1AA
Name	glycosylation, congenital disorder of, type Iaa (CDG1AA)
OMIM ID	617082
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NUS1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2018-07-18 22:50:59 +02:00 (CEST)
Date last edited	2021-10-14 19:33:00 +02:00 (CEST)

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