Disease #02434 (CDG1B (glycosylation, congenital disorder of, type Ib (CDG-1B)), OMIM:602579)

Official abbreviation CDG1B
Name glycosylation, congenital disorder of, type Ib (CDG-1B)
OMIM ID 602579
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease -
Associated with 1 gene MPI
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

6 entries on 1 page. Showing entries 1 - 6.
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00229636 - - - ? - Netherlands - - - - - CDG1B - MPI MPI 2 1 Gert Matthijs
00229637 - - - ? - Germany - - - - - CDG1B - MPI MPI 2 1 Gert Matthijs
00229638 - - - ? - France - - - - - CDG1B - MPI MPI 2 1 Gert Matthijs
00229639 - - - ? - United Kingdom (Great Britain) - - - - - CDG1B - MPI MPI 1 1 Gert Matthijs
00229640 - - - ? - United States - - - - - CDG1B - MPI MPI 2 1 Gert Matthijs
00229641 - - - ? - Poland - - - - - CDG1B - MPI MPI 2 1 Gert Matthijs
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