Disease #02341

Official abbreviation CDG-1D
Name glycosylation, congenital disorder of, type Id (CDG-1D)
OMIM ID 601110
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene ALG3
Associated tissues -
Disease features -
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00081089 - Trujillano et al., submitted unaffected parents - - - - - 0 - - CDG-1D Congenital disorder of glycosylation, type Id (OMIM:601110) ALG3 ALG3 1 1 Daniel Trujillano
00249657 - - - ? - Germany - - 0 - - CDG-1D - ALG3 ALG3 1 1 Gert Matthijs
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