Disease #02341 (CDG1D (glycosylation, congenital disorder of, type Id (CDG-1D)), OMIM:601110)

Official abbreviation CDG1D
Name glycosylation, congenital disorder of, type Id (CDG-1D)
OMIM ID 601110
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene ALG3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00081089 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - CDG1D Congenital disorder of glycosylation, type Id (OMIM:601110) ALG3 ALG3 1 1 Daniel Trujillano
00249657 - - - ? - Germany - - - - - CDG1D - ALG3 ALG3 1 1 Gert Matthijs
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