Disease #02735

Official abbreviation CDG-1H
Name glycosylation, congenital disorder of, type Ih (CDG-1H)
OMIM ID 608104
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 0
Associated with 1 gene ALG8
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Disease features -
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00249642 - - - ? - United Kingdom (Great Britain) - - 0 - - CDG-1H - ALG8 ALG8 2 1 Gert Matthijs
00249643 - - - ? - United Kingdom (Great Britain) - - 0 - - CDG-1H - ALG8 ALG8 2 1 Gert Matthijs
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