Disease #05973 (CDG1CC (glycosylation, congenital disorder of, type Icc (CDG1CC)), OMIM:301031)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	CDG1CC
Name	glycosylation, congenital disorder of, type Icc (CDG1CC)
OMIM ID	301031
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MAGT1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-10-15 10:30:05 +02:00 (CEST)
Date last edited	2021-10-15 10:30:56 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.