Disease #02735 (CDG1H (glycosylation, congenital disorder of, type Ih (CDG-1H)), OMIM:608104)

Official abbreviation CDG1H
Name glycosylation, congenital disorder of, type Ih (CDG-1H)
OMIM ID 608104
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene ALG8
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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00249642 - - - ? - United Kingdom (Great Britain) - - - - - CDG1H - ALG8 ALG8 2 1 Gert Matthijs
00249643 - - - ? - United Kingdom (Great Britain) - - - - - CDG1H - ALG8 ALG8 2 1 Gert Matthijs
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