Disease #02635 (CDG1G (glycosylation, congenital disorder of, type Ig (CDG-1G)), OMIM:607143)

Official abbreviation CDG1G
Name glycosylation, congenital disorder of, type Ig (CDG-1G)
OMIM ID 607143
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 1
Associated with 1 gene ALG12
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

3 entries on 1 page. Showing entries 1 - 3.
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00248371 - - - M ? (Italy) - - - - - CDG1G - - ALG12 2 1 Emanuele Agolini
00249658 - - - ? - Denmark - - - - - CDG1G - ALG12 ALG12 2 1 Gert Matthijs
00306212 112 - - M - China - - - - - CDG1G - ALG12 ALG12 2 1 Sha Hong
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